Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	51364
Common Name:	3',5'-cyclic IMP
Systematic Name:	inosine 3',5'-(hydrogen phosphate)
RefMet Name:	3',5' cyclic IMP
Synonyms:	cyclic IMP; inosine cyclic 3',5'-(hydrogen phosphate) [PubChem Synonyms]
Exact Mass:	330.0365 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C10H11N4O7P
InChIKey:	DMJWGQPYNRPLGA-KQYNXXCUSA-N
ClassyFire superclass:	Nucleosides, nucleotides, and analogues
ClassyFire class:	Purine nucleotides
ClassyFire subclass:	Cyclic purine nucleotides
ClassyFire direct parent:	3',5'-cyclic purine nucleotides
SMILES:	C1[C@@H]2[C@H]([C@H]([C@H](n3cnc4c3ncnc4O)O2)O)OP(=O)(O)O1
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

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PubChem CID:	135398663
CHEBI ID:	27541

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y
NPClassifier classification: "NPClassifier: A Deep Neural Network-Based Structural Classification Tool for Natural Products", Kim HW, Wang M, Leber CA, Nothias LF, Reher R, Kang KB, van der Hooft JJJ, Dorrestein PC, Gerwick WH and Cottrell GW. J Nat Prod. 2021 Nov 26;84(11):2795-2807.DOI: 10.1021/acs.jnatprod.1c00399.