ID: ALA3417157

Max Phase: Preclinical

Molecular Formula: C37H53ClO5

Molecular Weight: 613.28

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC1(C)CC[C@]2(C(=O)OCc3ccc(Cl)cc3)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)[C@@H](O)[C@H](O)[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]2C1

Standard InChI:  InChI=1S/C37H53ClO5/c1-32(2)16-18-37(31(42)43-21-22-8-10-23(38)11-9-22)19-17-34(5)24(25(37)20-32)12-13-27-35(34,6)15-14-26-33(3,4)29(40)28(39)30(41)36(26,27)7/h8-12,25-30,39-41H,13-21H2,1-7H3/t25-,26-,27-,28+,29-,30-,34+,35+,36-,37-/m0/s1

Standard InChI Key:  JVERPENVYQIBRL-UJKFIUSSSA-N

Associated Targets(non-human)

Streptomyces scabiei 197 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus spizizenii 1898 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 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

Properties

Molecular Weight: 613.28Molecular Weight (Monoisotopic): 612.3582AlogP: 7.49#Rotatable Bonds: 3
Polar Surface Area: 86.99Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.98CX Basic pKa: CX LogP: 7.08CX LogD: 7.08
Aromatic Rings: 1Heavy Atoms: 43QED Weighted: 0.24Np Likeness Score: 2.37

References

1. Huang L, Luo H, Li Q, Wang D, Zhang J, Hao X, Yang X..  (2015)  Pentacyclic triterpene derivatives possessing polyhydroxyl ring A inhibit gram-positive bacteria growth by regulating metabolism and virulence genes expression.,  95  [PMID:25794790] [10.1016/j.ejmech.2015.01.015]

Source