ID: ALA4644418

Max Phase: Preclinical

Molecular Formula: C31H50O4

Molecular Weight: 486.74

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C=C(C)[C@@H]1CC[C@@H]2[C@]3(CC[C@]4(C)[C@@H]([C@H](CO)CC/C=C(/C)CO)CC[C@@]24C)C[C@]13CCC(=O)OC

Standard InChI:  InChI=1S/C31H50O4/c1-21(2)24-10-11-26-29(5)14-12-25(23(19-33)9-7-8-22(3)18-32)28(29,4)16-17-31(26)20-30(24,31)15-13-27(34)35-6/h8,23-26,32-33H,1,7,9-20H2,2-6H3/b22-8-/t23-,24-,25+,26-,28+,29-,30+,31-/m0/s1

Standard InChI Key:  RBNIIYHAQIYTNT-YRUHVZQTSA-N

Associated Targets(non-human)

NRK-52E 51 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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

Properties

Molecular Weight: 486.74Molecular Weight (Monoisotopic): 486.3709AlogP: 6.46#Rotatable Bonds: 10
Polar Surface Area: 66.76Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.23CX LogD: 5.23
Aromatic Rings: 0Heavy Atoms: 35QED Weighted: 0.27Np Likeness Score: 3.31

References

1. Cao YG, Zhang YL, Zeng MN, Qi M, Ren YJ, Liu YL, Zhao X, Zheng XK, Feng WS..  (2020)  Renoprotective Mono- and Triterpenoids from the Fruit of Gardenia jasminoides.,  83  (4): [PMID:32141747] [10.1021/acs.jnatprod.9b01119]

Source