28-O-beta-D-glucopyranosylbetulinic acid

ID: ALA4070749

Chembl Id: CHEMBL4070749

PubChem CID: 137639091

Max Phase: Preclinical

Molecular Formula: C36H58O8

Molecular Weight: 618.85

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  C=C(C)[C@@H]1CC[C@]2(C(=O)O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)CC[C@]3(C)C(CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@H]12

Standard InChI:  InChI=1S/C36H58O8/c1-19(2)20-10-15-36(31(42)44-30-29(41)28(40)27(39)22(18-37)43-30)17-16-34(6)21(26(20)36)8-9-24-33(5)13-12-25(38)32(3,4)23(33)11-14-35(24,34)7/h20-30,37-41H,1,8-18H2,2-7H3/t20-,21?,22+,23-,24+,25-,26-,27+,28-,29+,30-,33-,34+,35+,36-/m0/s1

Standard InChI Key:  GPYJMOFNKRFSHT-JHSBWUGHSA-N

Alternative Forms

  1. Parent:

    ALA4070749

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Associated Targets(Human)

F3 Tclin Coagulation factor III (225 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 618.85Molecular Weight (Monoisotopic): 618.4132AlogP: 4.35#Rotatable Bonds: 4
Polar Surface Area: 136.68Molecular Species: NEUTRALHBA: 8HBD: 5
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.20CX Basic pKa: CX LogP: 4.37CX LogD: 4.37
Aromatic Rings: Heavy Atoms: 44QED Weighted: 0.23Np Likeness Score: 2.90

References

1. Wang WW, Xu SH, Zhao YZ, Zhang C, Zhang YY, Yu BY, Zhang J..  (2017)  Microbial hydroxylation and glycosylation of pentacyclic triterpenes as inhibitors on tissue factor procoagulant activity.,  27  (4): [PMID:28109788] [10.1016/j.bmcl.2016.12.066]

Source