FMB

FORMYCIN B

Created: 1999-07-08
Last modified:  2011-06-04

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Chemical Details

Formal Charge0
Atom Count31
Chiral Atom Count4
Bond Count33
Aromatic Bond Count10
2D diagram of FMB

Chemical Component Summary

NameFORMYCIN B
Systematic Name (OpenEye OEToolkits)3-[(2S,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,6-dihydropyrazolo[5,4-e]pyrimidin-7-one
FormulaC10 H12 N4 O5
Molecular Weight268.226
TypeNON-POLYMER

Chemical Descriptors

TypeProgram Version Descriptor
SMILESACDLabs10.04O=C1NC=Nc2c1nnc2C3OC(CO)C(O)C3O
SMILESCACTVS3.341OC[CH]1O[CH]([CH](O)[CH]1O)c2n[nH]c3C(=O)NC=Nc23
SMILESOpenEye OEToolkits1.5.0C1=Nc2c(n[nH]c2C(=O)N1)C3C(C(C(O3)CO)O)O
Canonical SMILESCACTVS3.341 OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)c2n[nH]c3C(=O)NC=Nc23
Canonical SMILESOpenEye OEToolkits1.5.0 C1=Nc2c(n[nH]c2C(=O)N1)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O
InChIInChI1.03 InChI=1S/C10H12N4O5/c15-1-3-7(16)8(17)9(19-3)5-4-6(14-13-5)10(18)12-2-11-4/h2-3,7-9,15-17H,1H2,(H,13,14)(H,11,12,18)/t3-,7-,8-,9+/m1/s1
InChIKeyInChI1.03 MTCJZZBQNCXKAP-KSYZLYKTSA-N

Drug Info: DrugBank

DrugBank IDDB04198 
NameFormycin B
Groups experimental
SynonymsFormycin B
Categories
  • Nucleic Acids, Nucleotides, and Nucleosides
  • Nucleosides
  • Pyrimidine Nucleosides
  • Pyrimidines
  • Ribonucleosides

Drug Targets

NameTarget SequencePharmacological ActionActions
Purine nucleoside phosphorylase DeoD-typeMATPHINAEMGDFADVVLMPGDPLRAKYIAETFLEDAREVNNVRGMLGFT...unknown
Hypoxanthine-guanine phosphoribosyltransferaseMPREYEFAEKILFTEEEIRTRIMEVAKRIADDYKGKGLRPYVNPLVLISV...unknown
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682

Related Resource References

Resource NameReference
PubChem 5288221, 135449281, 72443
ChEMBL CHEMBL1232777
ChEBI CHEBI:42654
CCDC/CSD FORMYB01