ID: ALA4635003

Max Phase: Preclinical

Molecular Formula: C27H34O11

Molecular Weight: 534.56

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C=C1C(CO[C@@H]2O[C@H](COC(=O)/C=C/c3cc(OC)c(O)c(OC)c3)[C@@H](O)[C@H](O)[C@H]2O)=CC(=O)CC1(C)C

Standard InChI:  InChI=1S/C27H34O11/c1-14-16(10-17(28)11-27(14,2)3)12-37-26-25(33)24(32)23(31)20(38-26)13-36-21(29)7-6-15-8-18(34-4)22(30)19(9-15)35-5/h6-10,20,23-26,30-33H,1,11-13H2,2-5H3/b7-6+/t20-,23-,24+,25-,26-/m1/s1

Standard InChI Key:  SLJXZSBKZITVLH-JPTAAFBWSA-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: 534.56Molecular Weight (Monoisotopic): 534.2101AlogP: 1.27#Rotatable Bonds: 9
Polar Surface Area: 161.21Molecular Species: NEUTRALHBA: 11HBD: 4
#RO5 Violations: 2HBA (Lipinski): 11HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 9.29CX Basic pKa: CX LogP: 1.62CX LogD: 1.61
Aromatic Rings: 1Heavy Atoms: 38QED Weighted: 0.27Np Likeness Score: 1.65

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