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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 12:38:24 UTC

Update Date

2022-09-22 17:45:02 UTC

HMDB ID

HMDB0253783

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Ketanserin

Description

Ketanserin belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Ketanserin is a very strong basic compound (based on its pKa). It was discovered at Janssen Pharmaceutica in 1980. It has been used in cardiac surgery. The same research team found no significant correlation with age in their homogenate binding study. It has also been found to block the vesicular monoamine transporter 2 (VMAT2). With tritium (3H) radioactively labeled ketanserin is used as a radioligand for serotonin 5-HT2 receptors, e.g. in receptor binding assays and autoradiography. Ketanserin is a high-affinity non-selective antagonist of 5-HT2 receptors in rodents, with Ki values of 2–3 nM for the 5-HT2A receptor and 28 nM for the 5-HT2C receptor). However, due to the significant adverse effect burden, the authors concluded that ketanserin's utility for this indication is likely unbeneficial. Ketanserin (INN, USAN, BAN) (brand name Sufrexal; former developmental code name R41468) is a drug used clinically as an antihypertensive agent and in scientific research to study the serotonin system; specifically, the 5-HT2 receptor family. This compound has been identified in human blood as reported by (PMID: 31557052 ). Ketanserin is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Ketanserin is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1533004241521382D          

 29 32  0  0  0  0            999 V2000
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -0.4125    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 12 15  1  0  0  0  0
  3 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

HMDB0253783
     RDKit          3D
Ketanserin
 51 54  0  0  0  0  0  0  0  0999 V2000
    4.5892   -0.5196   -2.1383 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355   -0.1452   -0.9804 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1898   -0.2058    0.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8399    0.2582    1.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7291    0.1903    2.4318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9659   -0.3496    2.2084 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9029   -0.4579    3.1851 F   0  0  0  0  0  0  0  0  0  0  0  0
    7.3172   -0.8139    0.9646 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4537   -0.7599   -0.1036 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8455    0.3405   -0.8114 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1702    0.3780   -2.1552 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6743    0.2788   -2.0766 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2198   -0.7989   -1.2500 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9644   -0.5437   -0.5110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1732   -0.4252   -1.4359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3793   -0.1687   -0.6793 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1227   -1.2095   -0.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7109   -2.3714   -0.5018 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2520   -0.9851    0.4709 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6970    0.2511    0.7624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8481    0.5001    1.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2606    1.7890    1.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5143    2.8465    1.2988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3619    2.6050    0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9573    1.3191    0.3177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8067    1.0826   -0.3984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0763    2.0234   -0.8393 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2223   -1.4941   -0.5506 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395   -0.5658    0.1646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8841    0.6923    1.5696 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4882    0.5474    3.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2945   -1.2437    0.7773 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7095   -1.1208   -1.0947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9062    1.3463   -0.3366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4130    1.3579   -2.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5687   -0.4027   -2.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2244    1.2178   -1.6963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2774    0.1241   -3.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1627   -1.4146    0.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9306    0.3734    0.1073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2639   -1.3092   -2.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9774    0.4701   -2.0824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8042   -1.8149    0.8026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4330   -0.3523    1.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1809    1.9778    2.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7846    3.8762    1.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7370    3.4302    0.2072 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8448   -2.1661   -1.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7224   -2.1303    0.2369 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9068   -1.2302    0.6677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6644   -0.0071    0.9851 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  2 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 13 28  1  0
 28 29  1  0
  9  3  1  0
 29 10  1  0
 26 16  1  0
 25 20  1  0
  4 30  1  0
  5 31  1  0
  8 32  1  0
  9 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 19 43  1  0
 21 44  1  0
 22 45  1  0
 23 46  1  0
 24 47  1  0
 28 48  1  0
 28 49  1  0
 29 50  1  0
 29 51  1  0
M  END


  Mrv1533004241521382D          

 29 32  0  0  0  0            999 V2000
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -0.4125    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 12 15  1  0  0  0  0
  3 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0253783

> <DATABASE_NAME>
hmdb

> <SMILES>
FC1=CC=C(C=C1)C(=O)C1CCN(CCN2C(=O)NC3=CC=CC=C3C2=O)CC1

> <INCHI_IDENTIFIER>
InChI=1S/C22H22FN3O3/c23-17-7-5-15(6-8-17)20(27)16-9-11-25(12-10-16)13-14-26-21(28)18-3-1-2-4-19(18)24-22(26)29/h1-8,16H,9-14H2,(H,24,29)

> <INCHI_KEY>
FPCCSQOGAWCVBH-UHFFFAOYSA-N

> <FORMULA>
C22H22FN3O3

> <MOLECULAR_WEIGHT>
395.434

> <EXACT_MASS>
395.164519743

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
39.88583845464984

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{2-[4-(4-fluorobenzoyl)piperidin-1-yl]ethyl}-1,2,3,4-tetrahydroquinazoline-2,4-dione

> <ALOGPS_LOGP>
2.92

> <JCHEM_LOGP>
3.609319796

> <ALOGPS_LOGS>
-3.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
16.566906004254218

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.424021035928964

> <JCHEM_PKA_STRONGEST_BASIC>
7.285732205758433

> <JCHEM_POLAR_SURFACE_AREA>
69.72

> <JCHEM_REFRACTIVITY>
109.10730000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.56e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ketanserin

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0253783
     RDKit          3D
Ketanserin
 51 54  0  0  0  0  0  0  0  0999 V2000
    4.5892   -0.5196   -2.1383 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355   -0.1452   -0.9804 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1898   -0.2058    0.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8399    0.2582    1.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7291    0.1903    2.4318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9659   -0.3496    2.2084 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9029   -0.4579    3.1851 F   0  0  0  0  0  0  0  0  0  0  0  0
    7.3172   -0.8139    0.9646 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4537   -0.7599   -0.1036 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8455    0.3405   -0.8114 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1702    0.3780   -2.1552 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6743    0.2788   -2.0766 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2198   -0.7989   -1.2500 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9644   -0.5437   -0.5110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1732   -0.4252   -1.4359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3793   -0.1687   -0.6793 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1227   -1.2095   -0.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7109   -2.3714   -0.5018 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2520   -0.9851    0.4709 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6970    0.2511    0.7624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8481    0.5001    1.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2606    1.7890    1.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5143    2.8465    1.2988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3619    2.6050    0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9573    1.3191    0.3177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8067    1.0826   -0.3984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0763    2.0234   -0.8393 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2223   -1.4941   -0.5506 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395   -0.5658    0.1646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8841    0.6923    1.5696 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4882    0.5474    3.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2945   -1.2437    0.7773 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7095   -1.1208   -1.0947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9062    1.3463   -0.3366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4130    1.3579   -2.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5687   -0.4027   -2.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2244    1.2178   -1.6963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2774    0.1241   -3.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1627   -1.4146    0.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9306    0.3734    0.1073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2639   -1.3092   -2.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9774    0.4701   -2.0824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8042   -1.8149    0.8026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4330   -0.3523    1.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1809    1.9778    2.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7846    3.8762    1.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7370    3.4302    0.2072 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8448   -2.1661   -1.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7224   -2.1303    0.2369 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9068   -1.2302    0.6677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6644   -0.0071    0.9851 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  2 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 13 28  1  0
 28 29  1  0
  9  3  1  0
 29 10  1  0
 26 16  1  0
 25 20  1  0
  4 30  1  0
  5 31  1  0
  8 32  1  0
  9 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 19 43  1  0
 21 44  1  0
 22 45  1  0
 23 46  1  0
 24 47  1  0
 28 48  1  0
 28 49  1  0
 29 50  1  0
 29 51  1  0
M  END

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -2.667   0.000   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -6.668   3.850   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -10.669   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -9.336   2.310   0.000  0.00  0.00           C+0
HETATM   15  F   UNK     0     -12.003  -0.770   0.000  0.00  0.00           F+0
HETATM   16  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       1.334  -0.770   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       2.667  -3.080   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   16                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15   12                                                            
CONECT   16    3   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   28                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   18   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

COMPND    HMDB0253783
HETATM    1  O1  UNL     1       4.589  -0.520  -2.138  1.00  0.00           O  
HETATM    2  C1  UNL     1       4.235  -0.145  -0.980  1.00  0.00           C  
HETATM    3  C2  UNL     1       5.190  -0.206   0.135  1.00  0.00           C  
HETATM    4  C3  UNL     1       4.840   0.258   1.378  1.00  0.00           C  
HETATM    5  C4  UNL     1       5.729   0.190   2.432  1.00  0.00           C  
HETATM    6  C5  UNL     1       6.966  -0.350   2.208  1.00  0.00           C  
HETATM    7  F1  UNL     1       7.903  -0.458   3.185  1.00  0.00           F  
HETATM    8  C6  UNL     1       7.317  -0.814   0.965  1.00  0.00           C  
HETATM    9  C7  UNL     1       6.454  -0.760  -0.104  1.00  0.00           C  
HETATM   10  C8  UNL     1       2.846   0.340  -0.811  1.00  0.00           C  
HETATM   11  C9  UNL     1       2.170   0.378  -2.155  1.00  0.00           C  
HETATM   12  C10 UNL     1       0.674   0.279  -2.077  1.00  0.00           C  
HETATM   13  N1  UNL     1       0.220  -0.799  -1.250  1.00  0.00           N  
HETATM   14  C11 UNL     1      -0.964  -0.544  -0.511  1.00  0.00           C  
HETATM   15  C12 UNL     1      -2.173  -0.425  -1.436  1.00  0.00           C  
HETATM   16  N2  UNL     1      -3.379  -0.169  -0.679  1.00  0.00           N  
HETATM   17  C13 UNL     1      -4.123  -1.209  -0.232  1.00  0.00           C  
HETATM   18  O2  UNL     1      -3.711  -2.371  -0.502  1.00  0.00           O  
HETATM   19  N3  UNL     1      -5.252  -0.985   0.471  1.00  0.00           N  
HETATM   20  C14 UNL     1      -5.697   0.251   0.762  1.00  0.00           C  
HETATM   21  C15 UNL     1      -6.848   0.500   1.478  1.00  0.00           C  
HETATM   22  C16 UNL     1      -7.261   1.789   1.748  1.00  0.00           C  
HETATM   23  C17 UNL     1      -6.514   2.846   1.299  1.00  0.00           C  
HETATM   24  C18 UNL     1      -5.362   2.605   0.583  1.00  0.00           C  
HETATM   25  C19 UNL     1      -4.957   1.319   0.318  1.00  0.00           C  
HETATM   26  C20 UNL     1      -3.807   1.083  -0.398  1.00  0.00           C  
HETATM   27  O3  UNL     1      -3.076   2.023  -0.839  1.00  0.00           O  
HETATM   28  C21 UNL     1       1.222  -1.494  -0.551  1.00  0.00           C  
HETATM   29  C22 UNL     1       2.139  -0.566   0.165  1.00  0.00           C  
HETATM   30  H1  UNL     1       3.884   0.692   1.570  1.00  0.00           H  
HETATM   31  H2  UNL     1       5.488   0.547   3.432  1.00  0.00           H  
HETATM   32  H3  UNL     1       8.294  -1.244   0.777  1.00  0.00           H  
HETATM   33  H4  UNL     1       6.710  -1.121  -1.095  1.00  0.00           H  
HETATM   34  H5  UNL     1       2.906   1.346  -0.337  1.00  0.00           H  
HETATM   35  H6  UNL     1       2.413   1.358  -2.614  1.00  0.00           H  
HETATM   36  H7  UNL     1       2.569  -0.403  -2.834  1.00  0.00           H  
HETATM   37  H8  UNL     1       0.224   1.218  -1.696  1.00  0.00           H  
HETATM   38  H9  UNL     1       0.277   0.124  -3.098  1.00  0.00           H  
HETATM   39  H10 UNL     1      -1.163  -1.415   0.147  1.00  0.00           H  
HETATM   40  H11 UNL     1      -0.931   0.373   0.107  1.00  0.00           H  
HETATM   41  H12 UNL     1      -2.264  -1.309  -2.089  1.00  0.00           H  
HETATM   42  H13 UNL     1      -1.977   0.470  -2.082  1.00  0.00           H  
HETATM   43  H14 UNL     1      -5.804  -1.815   0.803  1.00  0.00           H  
HETATM   44  H15 UNL     1      -7.433  -0.352   1.830  1.00  0.00           H  
HETATM   45  H16 UNL     1      -8.181   1.978   2.319  1.00  0.00           H  
HETATM   46  H17 UNL     1      -6.785   3.876   1.478  1.00  0.00           H  
HETATM   47  H18 UNL     1      -4.737   3.430   0.207  1.00  0.00           H  
HETATM   48  H19 UNL     1       1.845  -2.166  -1.177  1.00  0.00           H  
HETATM   49  H20 UNL     1       0.722  -2.130   0.237  1.00  0.00           H  
HETATM   50  H21 UNL     1       2.907  -1.230   0.668  1.00  0.00           H  
HETATM   51  H22 UNL     1       1.664  -0.007   0.985  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   10
CONECT    3    4    4    9
CONECT    4    5   30
CONECT    5    6    6   31
CONECT    6    7    8
CONECT    8    9    9   32
CONECT    9   33
CONECT   10   11   29   34
CONECT   11   12   35   36
CONECT   12   13   37   38
CONECT   13   14   28
CONECT   14   15   39   40
CONECT   15   16   41   42
CONECT   16   17   26
CONECT   17   18   18   19
CONECT   19   20   43
CONECT   20   21   21   25
CONECT   21   22   44
CONECT   22   23   23   45
CONECT   23   24   46
CONECT   24   25   25   47
CONECT   25   26
CONECT   26   27   27
CONECT   28   29   48   49
CONECT   29   50   51
END

HMDB0253783
     RDKit          3D
Ketanserin
 51 54  0  0  0  0  0  0  0  0999 V2000
    4.5892   -0.5196   -2.1383 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355   -0.1452   -0.9804 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1898   -0.2058    0.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8399    0.2582    1.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7291    0.1903    2.4318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9659   -0.3496    2.2084 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9029   -0.4579    3.1851 F   0  0  0  0  0  0  0  0  0  0  0  0
    7.3172   -0.8139    0.9646 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4537   -0.7599   -0.1036 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8455    0.3405   -0.8114 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1702    0.3780   -2.1552 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6743    0.2788   -2.0766 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2198   -0.7989   -1.2500 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9644   -0.5437   -0.5110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1732   -0.4252   -1.4359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3793   -0.1687   -0.6793 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1227   -1.2095   -0.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7109   -2.3714   -0.5018 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2520   -0.9851    0.4709 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6970    0.2511    0.7624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8481    0.5001    1.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2606    1.7890    1.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5143    2.8465    1.2988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3619    2.6050    0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9573    1.3191    0.3177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8067    1.0826   -0.3984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0763    2.0234   -0.8393 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2223   -1.4941   -0.5506 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395   -0.5658    0.1646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8841    0.6923    1.5696 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4882    0.5474    3.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2945   -1.2437    0.7773 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7095   -1.1208   -1.0947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9062    1.3463   -0.3366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4130    1.3579   -2.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5687   -0.4027   -2.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2244    1.2178   -1.6963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2774    0.1241   -3.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1627   -1.4146    0.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9306    0.3734    0.1073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2639   -1.3092   -2.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9774    0.4701   -2.0824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8042   -1.8149    0.8026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4330   -0.3523    1.8295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1809    1.9778    2.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7846    3.8762    1.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7370    3.4302    0.2072 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8448   -2.1661   -1.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7224   -2.1303    0.2369 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9068   -1.2302    0.6677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6644   -0.0071    0.9851 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  2 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 13 28  1  0
 28 29  1  0
  9  3  1  0
 29 10  1  0
 26 16  1  0
 25 20  1  0
  4 30  1  0
  5 31  1  0
  8 32  1  0
  9 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 19 43  1  0
 21 44  1  0
 22 45  1  0
 23 46  1  0
 24 47  1  0
 28 48  1  0
 28 49  1  0
 29 50  1  0
 29 51  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
3-[2-[4-(4-Fluorobenzoyl)-1-piperidyl]ethyl]-1H-quinazoline-2,4-dione	ChEBI
Ketanserina	ChEBI
Ketanserine	ChEBI
Ketanserinum	ChEBI
3-(2-(4-(4-Fluorobenzoyl)piperidinol)ethyl)-2,4(1H,3H)-quinazolinedione	MeSH

Chemical Formula

C₂₂H₂₂FN₃O₃

Average Molecular Weight

395.434

Monoisotopic Molecular Weight

395.164519743

IUPAC Name

3-{2-[4-(4-fluorobenzoyl)piperidin-1-yl]ethyl}-1,2,3,4-tetrahydroquinazoline-2,4-dione

Traditional Name

ketanserin

CAS Registry Number

Not Available

SMILES

FC1=CC=C(C=C1)C(=O)C1CCN(CCN2C(=O)NC3=CC=CC=C3C2=O)CC1

InChI Identifier

InChI=1S/C22H22FN3O3/c23-17-7-5-15(6-8-17)20(27)16-9-11-25(12-10-16)13-14-26-21(28)18-3-1-2-4-19(18)24-22(26)29/h1-8,16H,9-14H2,(H,24,29)

InChI Key

FPCCSQOGAWCVBH-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Diazanaphthalene
Quinazoline
Benzoyl
Aryl alkyl ketone
Fluorobenzene
Halobenzene
Hydroxypyrimidine
Pyrimidone
Aryl fluoride
Aryl halide
Monocyclic benzene moiety
Gamma-aminoketone
Piperidine
Pyrimidine
Benzenoid
Heteroaromatic compound
Lactam
Tertiary amine
Tertiary aliphatic amine
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Amine
Organonitrogen compound
Organofluoride
Organohalogen compound
Organic oxide
Hydrocarbon derivative
Organopnictogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

piperidines (CHEBI:6123 )
organofluorine compound (CHEBI:6123 )
aromatic ketone (CHEBI:6123 )
quinazolines (CHEBI:6123 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	2.92	ALOGPS
logP	3.61	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	11.42	ChemAxon
pKa (Strongest Basic)	7.29	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	69.72 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	109.11 m³·mol⁻¹	ChemAxon
Polarizability	39.89 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	193.535	30932474
DeepCCS	[M-H]-	191.177	30932474
DeepCCS	[M-2H]-	225.198	30932474
DeepCCS	[M+Na]+	200.426	30932474
AllCCS	[M+H]+	193.1	32859911
AllCCS	[M+H-H2O]+	190.5	32859911
AllCCS	[M+NH4]+	195.4	32859911
AllCCS	[M+Na]+	196.1	32859911
AllCCS	[M-H]-	193.2	32859911
AllCCS	[M+Na-2H]-	193.2	32859911
AllCCS	[M+HCOO]-	193.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Ketanserin	FC1=CC=C(C=C1)C(=O)C1CCN(CCN2C(=O)NC3=CC=CC=C3C2=O)CC1	4237.9	Standard polar	33892256
Ketanserin	FC1=CC=C(C=C1)C(=O)C1CCN(CCN2C(=O)NC3=CC=CC=C3C2=O)CC1	3527.1	Standard non polar	33892256
Ketanserin	FC1=CC=C(C=C1)C(=O)C1CCN(CCN2C(=O)NC3=CC=CC=C3C2=O)CC1	3627.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Ketanserin,1TMS,isomer #1	C[Si](C)(C)N1C(=O)N(CCN2CCC(C(=O)C3=CC=C(F)C=C3)CC2)C(=O)C2=CC=CC=C21	3406.1	Semi standard non polar	33892256
Ketanserin,1TMS,isomer #1	C[Si](C)(C)N1C(=O)N(CCN2CCC(C(=O)C3=CC=C(F)C=C3)CC2)C(=O)C2=CC=CC=C21	3194.5	Standard non polar	33892256
Ketanserin,1TMS,isomer #1	C[Si](C)(C)N1C(=O)N(CCN2CCC(C(=O)C3=CC=C(F)C=C3)CC2)C(=O)C2=CC=CC=C21	4234.3	Standard polar	33892256
Ketanserin,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N1C(=O)N(CCN2CCC(C(=O)C3=CC=C(F)C=C3)CC2)C(=O)C2=CC=CC=C21	3581.8	Semi standard non polar	33892256
Ketanserin,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N1C(=O)N(CCN2CCC(C(=O)C3=CC=C(F)C=C3)CC2)C(=O)C2=CC=CC=C21	3391.8	Standard non polar	33892256
Ketanserin,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N1C(=O)N(CCN2CCC(C(=O)C3=CC=C(F)C=C3)CC2)C(=O)C2=CC=CC=C21	4254.6	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Ketanserin GC-MS (Non-derivatized) - 70eV, Positive	splash10-00di-7950000000-74fc2a746ecc54e92943	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Ketanserin GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 10V, Positive-QTOF	splash10-0002-0219000000-78bf9d9276e44824d54c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 20V, Positive-QTOF	splash10-000i-0912000000-29399db0edad451149f2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 40V, Positive-QTOF	splash10-03dl-3900000000-b1898672b4a7b2b23a5b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 10V, Negative-QTOF	splash10-01ox-0609000000-d3c3bc35fe222b97c7c8	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 20V, Negative-QTOF	splash10-0006-1439000000-279eefb55f3e7f2ac984	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 40V, Negative-QTOF	splash10-0006-9820000000-8f95a266435787172658	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 10V, Negative-QTOF	splash10-0006-0009000000-37133899d8dc7c385562	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 20V, Negative-QTOF	splash10-0006-0309000000-52033eafdd30495390be	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 40V, Negative-QTOF	splash10-0297-5961000000-38afc0786a1f7ed525ba	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 10V, Positive-QTOF	splash10-0002-0009000000-0a62af1817793f2b6956	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 20V, Positive-QTOF	splash10-000i-0903000000-5980133a99d44b5b6844	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ketanserin 40V, Positive-QTOF	splash10-000i-1900000000-43dc6e5f3f18c054604a	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details
Urine	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	34436864	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

DB12465

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C07464

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Ketanserin

METLIN ID

Not Available

PubChem Compound

3822

PDB ID

Not Available

ChEBI ID

6123

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for Ketanserin (HMDB0253783)

MOL for HMDB0253783 (Ketanserin)

3D MOL for HMDB0253783 (Ketanserin)

3D SDF for HMDB0253783 (Ketanserin)

3D-SDF for HMDB0253783 (Ketanserin)

PDB for HMDB0253783 (Ketanserin)

3D PDB for HMDB0253783 (Ketanserin)

SMILES for HMDB0253783 (Ketanserin)

INCHI for HMDB0253783 (Ketanserin)

Structure for HMDB0253783 (Ketanserin)

3D Structure for HMDB0253783 (Ketanserin)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra