Record Information |
---|
Version | 5.0 |
---|
Status | Detected but not Quantified |
---|
Creation Date | 2009-02-04 15:11:57 UTC |
---|
Update Date | 2022-09-22 18:34:20 UTC |
---|
HMDB ID | HMDB0011691 |
---|
Secondary Accession Numbers | |
---|
Metabolite Identification |
---|
Common Name | Cytidine 2',3'-cyclic phosphate |
---|
Description | Cytidine 2',3'-cyclic phosphate is a cytidine nucleotide containing a pyrophosphate group esterified to C2 and C3(cyclic) of the sugar moiety. A cyclic nucleotide is any nucleotide in which the phosphate group is bonded to two of the sugar's hydroxyl groups, forming a cyclical or ring structure. 2',3' cyclic CMP is a substrate for 2',3'-cyclic-nucleotide 3'-phosphodiesterase (EC 3.1.4.37). This enzyme (also called CNP) catalyzes the chemical reaction: nucleoside 2',3'-cyclic phosphate + H2O <-> nucleoside 2'-phosphate. CNP is a myelin-associated enzyme that makes up 4% of total CNS myelin protein, and is thought to undergo significant age-associated changes. The absence of CNP causes axonal swelling and neuronal degeneration. The biological role of cyclic 2',3' monophosphates is not clear, although it is thought to have something to do with neuronal stasis or development. |
---|
Structure | NC1=NC(=O)N(C=C1)C1O[C@H](CO)[C@H]2OP(O)(=O)O[C@@H]12 InChI=1S/C9H12N3O7P/c10-5-1-2-12(9(14)11-5)8-7-6(4(3-13)17-8)18-20(15,16)19-7/h1-2,4,6-8,13H,3H2,(H,15,16)(H2,10,11,14)/t4-,6-,7-,8?/m1/s1 |
---|
Synonyms | Value | Source |
---|
2',3' Cyclic CMP | HMDB | 2',3' Cyclic-CMP | HMDB | Cyclic(2',3')-CMP | HMDB | Cytidine-2',3'-cyclophosphate | HMDB | Cytidine 2',3'-cyclic phosphoric acid | Generator |
|
---|
Chemical Formula | C9H12N3O7P |
---|
Average Molecular Weight | 305.1812 |
---|
Monoisotopic Molecular Weight | 305.041286265 |
---|
IUPAC Name | 1-[(3aR,6R,6aR)-2-hydroxy-6-(hydroxymethyl)-2-oxo-tetrahydro-2H-2λ⁵-furo[3,4-d][1,3,2]dioxaphosphol-4-yl]-4-amino-1,2-dihydropyrimidin-2-one |
---|
Traditional Name | 1-[(3aR,6R,6aR)-2-hydroxy-6-(hydroxymethyl)-2-oxo-tetrahydro-2λ⁵-furo[3,4-d][1,3,2]dioxaphosphol-4-yl]-4-aminopyrimidin-2-one |
---|
CAS Registry Number | 15718-51-1 |
---|
SMILES | NC1=NC(=O)N(C=C1)C1O[C@H](CO)[C@H]2OP(O)(=O)O[C@@H]12 |
---|
InChI Identifier | InChI=1S/C9H12N3O7P/c10-5-1-2-12(9(14)11-5)8-7-6(4(3-13)17-8)18-20(15,16)19-7/h1-2,4,6-8,13H,3H2,(H,15,16)(H2,10,11,14)/t4-,6-,7-,8?/m1/s1 |
---|
InChI Key | NMPZCCZXCOMSDQ-ZRTZXPPTSA-N |
---|
Chemical Taxonomy |
---|
Description | Belongs to the class of organic compounds known as peptides. Peptides are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another. |
---|
Kingdom | Organic compounds |
---|
Super Class | Organic acids and derivatives |
---|
Class | Carboxylic acids and derivatives |
---|
Sub Class | Amino acids, peptides, and analogues |
---|
Direct Parent | Peptides |
---|
Alternative Parents | |
---|
Substituents | - Alpha peptide
- N-acyl-alpha-amino acid
- N-acyl-alpha amino acid or derivatives
- Tetracarboxylic acid or derivatives
- Alpha-amino acid
- Alpha-amino acid or derivatives
- L-alpha-amino acid
- Amino acid or derivatives
- Amino acid
- Dialkyldisulfide
- Organic disulfide
- Carboximidic acid
- Carboximidic acid derivative
- Carboxylic acid
- Organic 1,3-dipolar compound
- Propargyl-type 1,3-dipolar organic compound
- Sulfenyl compound
- Amine
- Hydrocarbon derivative
- Organic oxide
- Primary aliphatic amine
- Organic oxygen compound
- Organic nitrogen compound
- Organonitrogen compound
- Organooxygen compound
- Organosulfur compound
- Organopnictogen compound
- Primary amine
- Carbonyl group
- Aliphatic acyclic compound
|
---|
Molecular Framework | Aliphatic acyclic compounds |
---|
External Descriptors | |
---|
Ontology |
---|
Physiological effect | Not Available |
---|
Disposition | |
---|
Process | Not Available |
---|
Role | Not Available |
---|
Physical Properties |
---|
State | Solid |
---|
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 | Experimental Collision Cross Sections |
---|
Predicted Molecular Properties | |
---|
Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
---|
Cytidine 2',3'-cyclic phosphate,1TMS,isomer #1 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N)=NC2=O)[C@@H]2OP(=O)(O)O[C@H]12 | 2770.2 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,1TMS,isomer #2 | C[Si](C)(C)OP1(=O)O[C@H]2C(N3C=CC(N)=NC3=O)O[C@H](CO)[C@H]2O1 | 2774.7 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,1TMS,isomer #3 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O)O[C@@H]23)C=C1 | 2824.7 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #1 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C)O[C@H]12 | 2779.9 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #1 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C)O[C@H]12 | 2805.4 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #1 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C)O[C@H]12 | 3897.5 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #2 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C)[C@H]3OP(=O)(O)O[C@@H]23)C=C1 | 2838.7 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #2 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C)[C@H]3OP(=O)(O)O[C@@H]23)C=C1 | 2801.7 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #2 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C)[C@H]3OP(=O)(O)O[C@@H]23)C=C1 | 3957.7 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #3 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O[Si](C)(C)C)O[C@@H]23)C=C1 | 2834.6 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #3 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O[Si](C)(C)C)O[C@@H]23)C=C1 | 2810.7 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #3 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O[Si](C)(C)C)O[C@@H]23)C=C1 | 3762.3 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #4 | C[Si](C)(C)N(C1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O)O[C@@H]23)C=C1)[Si](C)(C)C | 2798.8 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #4 | C[Si](C)(C)N(C1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O)O[C@@H]23)C=C1)[Si](C)(C)C | 2868.5 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TMS,isomer #4 | C[Si](C)(C)N(C1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O)O[C@@H]23)C=C1)[Si](C)(C)C | 3930.6 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TMS,isomer #1 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C)[C@H]3OP(=O)(O[Si](C)(C)C)O[C@@H]23)C=C1 | 2867.5 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TMS,isomer #1 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C)[C@H]3OP(=O)(O[Si](C)(C)C)O[C@@H]23)C=C1 | 2869.8 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TMS,isomer #1 | C[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C)[C@H]3OP(=O)(O[Si](C)(C)C)O[C@@H]23)C=C1 | 3571.7 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TMS,isomer #2 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]2OP(=O)(O)O[C@H]12 | 2797.8 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TMS,isomer #2 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]2OP(=O)(O)O[C@H]12 | 2907.6 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TMS,isomer #2 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]2OP(=O)(O)O[C@H]12 | 3613.2 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TMS,isomer #3 | C[Si](C)(C)OP1(=O)O[C@H]2C(N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)O[C@H](CO)[C@H]2O1 | 2822.6 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TMS,isomer #3 | C[Si](C)(C)OP1(=O)O[C@H]2C(N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)O[C@H](CO)[C@H]2O1 | 2931.5 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TMS,isomer #3 | C[Si](C)(C)OP1(=O)O[C@H]2C(N3C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC3=O)O[C@H](CO)[C@H]2O1 | 3452.1 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,4TMS,isomer #1 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C)O[C@H]12 | 2837.1 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,4TMS,isomer #1 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C)O[C@H]12 | 2944.6 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,4TMS,isomer #1 | C[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C)O[C@H]12 | 3283.4 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,1TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N)=NC2=O)[C@@H]2OP(=O)(O)O[C@H]12 | 2988.8 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,1TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OP1(=O)O[C@H]2C(N3C=CC(N)=NC3=O)O[C@H](CO)[C@H]2O1 | 3003.4 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,1TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O)O[C@@H]23)C=C1 | 3083.3 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@H]12 | 3191.4 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@H]12 | 3228.6 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@H]12 | 4041.5 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H]3OP(=O)(O)O[C@@H]23)C=C1 | 3294.0 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H]3OP(=O)(O)O[C@@H]23)C=C1 | 3270.5 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H]3OP(=O)(O)O[C@@H]23)C=C1 | 4053.2 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@@H]23)C=C1 | 3311.1 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@@H]23)C=C1 | 3245.6 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@@H]23)C=C1 | 3922.0 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)N(C1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O)O[C@@H]23)C=C1)[Si](C)(C)C(C)(C)C | 3224.4 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)N(C1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O)O[C@@H]23)C=C1)[Si](C)(C)C(C)(C)C | 3305.8 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,2TBDMS,isomer #4 | CC(C)(C)[Si](C)(C)N(C1=NC(=O)N(C2O[C@H](CO)[C@H]3OP(=O)(O)O[C@@H]23)C=C1)[Si](C)(C)C(C)(C)C | 3957.0 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H]3OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@@H]23)C=C1 | 3504.3 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H]3OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@@H]23)C=C1 | 3470.1 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)NC1=NC(=O)N(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H]3OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@@H]23)C=C1 | 3826.1 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]2OP(=O)(O)O[C@H]12 | 3432.4 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]2OP(=O)(O)O[C@H]12 | 3543.1 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TBDMS,isomer #2 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]2OP(=O)(O)O[C@H]12 | 3776.6 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OP1(=O)O[C@H]2C(N3C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)O[C@H](CO)[C@H]2O1 | 3421.6 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OP1(=O)O[C@H]2C(N3C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)O[C@H](CO)[C@H]2O1 | 3522.2 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,3TBDMS,isomer #3 | CC(C)(C)[Si](C)(C)OP1(=O)O[C@H]2C(N3C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)O[C@H](CO)[C@H]2O1 | 3664.4 | Standard polar | 33892256 | Cytidine 2',3'-cyclic phosphate,4TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@H]12 | 3582.0 | Semi standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,4TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@H]12 | 3712.6 | Standard non polar | 33892256 | Cytidine 2',3'-cyclic phosphate,4TBDMS,isomer #1 | CC(C)(C)[Si](C)(C)OC[C@H]1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]2OP(=O)(O[Si](C)(C)C(C)(C)C)O[C@H]12 | 3576.4 | Standard polar | 33892256 |
|
---|
| GC-MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
---|
Predicted GC-MS | Predicted GC-MS Spectrum - Cytidine 2',3'-cyclic phosphate GC-MS (Non-derivatized) - 70eV, Positive | splash10-00rx-5940000000-8ab4c4a156dd13eee927 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Cytidine 2',3'-cyclic phosphate GC-MS (1 TMS) - 70eV, Positive | splash10-00di-3913000000-33e0f0bba64d9939e84e | 2017-10-06 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - Cytidine 2',3'-cyclic phosphate GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum |
MS/MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
---|
Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 10V, Positive-QTOF | splash10-03di-0901000000-f9f0fdfd685c0f6d0009 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 20V, Positive-QTOF | splash10-03di-0900000000-dad12eb9fc7a3373782c | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 35V, Negative-QTOF | splash10-03di-0900000000-6e1a86cabcec8891dda9 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 40V, Positive-QTOF | splash10-03di-4900000000-aecd73e537bb4318b1c3 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 20V, Positive-QTOF | splash10-03di-1900000000-b74f28f59440ae1f96f5 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 40V, Positive-QTOF | splash10-03di-3900000000-9cc2cbbabcad93d3efec | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 10V, Positive-QTOF | splash10-03di-0900000000-72e18b487faf7c919791 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 35V, Positive-QTOF | splash10-03di-0900000000-3b3614c0d13e95e4d276 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 20V, Negative-QTOF | splash10-03di-0900000000-15c4e619992ee25f8e94 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 10V, Negative-QTOF | splash10-03di-0901000000-7ef02eb4f51fe6099399 | 2021-09-20 | HMDB team, MONA | View Spectrum | Experimental LC-MS/MS | LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 40V, Negative-QTOF | splash10-03xu-9600000000-2921e887ac0b2dfcf98e | 2021-09-20 | HMDB team, MONA | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 10V, Positive-QTOF | splash10-03di-0901000000-e7f102f4bea63f5e5fda | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 20V, Positive-QTOF | splash10-03di-2900000000-cb3d80cc5dffe05f6888 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 40V, Positive-QTOF | splash10-03di-9600000000-6f0a550e121f5621a2f4 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 10V, Negative-QTOF | splash10-0nmi-1394000000-318f2cd988d67fcae4ca | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 20V, Negative-QTOF | splash10-03di-7971000000-a038ae20ec94c0e427e7 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 40V, Negative-QTOF | splash10-0006-9100000000-a171fcfbd0db4fdcd822 | 2017-09-01 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 10V, Negative-QTOF | splash10-0w29-0409000000-f8f0a161b78ae9d4d448 | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 20V, Negative-QTOF | splash10-01ox-9543000000-63b886b4a09466e8c05b | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 40V, Negative-QTOF | splash10-000x-9250000000-0c74f4f2bc95cd02b0f7 | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 10V, Positive-QTOF | splash10-03di-0903000000-88b3fcac211e9ba6e75e | 2021-09-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 20V, Positive-QTOF | splash10-03di-1902000000-4245b167806855aff9e7 | 2021-09-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - Cytidine 2',3'-cyclic phosphate 40V, Positive-QTOF | splash10-03di-4920000000-8f8af5c215ccf5b8e0d2 | 2021-09-25 | Wishart Lab | View Spectrum |
NMR SpectraSpectrum Type | Description | Deposition Date | Source | View |
---|
Predicted 1D NMR | 13C NMR Spectrum (1D, 100 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 100 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 1000 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 1000 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 200 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 200 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 300 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 300 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 400 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 400 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 500 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 500 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 600 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 600 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 700 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 700 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 800 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 800 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 13C NMR Spectrum (1D, 900 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum | Predicted 1D NMR | 1H NMR Spectrum (1D, 900 MHz, D2O, predicted) | 2021-09-25 | Wishart Lab | View Spectrum |
|
---|