ID: ALA5188803

Max Phase: Preclinical

Molecular Formula: C27H38O7

Molecular Weight: 474.59

Associated Items:

Representations

Canonical SMILES:  CC(=O)O[C@@]12[C@H](OC(=O)CC(C)C)[C@@H](C)[C@]3(O)[C@@H]4C=C(C)C(=O)[C@@H]4[C@@H](O)C(C)=C[C@H]3[C@@H]1C2(C)C

Standard InChI:  InChI=1S/C27H38O7/c1-12(2)9-19(29)33-24-15(5)26(32)17-10-13(3)21(30)20(17)22(31)14(4)11-18(26)23-25(7,8)27(23,24)34-16(6)28/h10-12,15,17-18,20,22-24,31-32H,9H2,1-8H3/t15-,17-,18+,20-,22+,23-,24-,26+,27-/m1/s1

Standard InChI Key:  WVGNWDVXOUWMCG-NYGUZCGBSA-N

Associated Targets(non-human)

Human immunodeficiency virus 3636 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 474.59Molecular Weight (Monoisotopic): 474.2618AlogP: 2.98#Rotatable Bonds: 4
Polar Surface Area: 110.13Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.72CX Basic pKa: CX LogP: 2.60CX LogD: 2.60
Aromatic Rings: 0Heavy Atoms: 34QED Weighted: 0.48Np Likeness Score: 2.91

References

1. Tanaka N, Takahashi S, Yoshino Y, Nakatani M, Ahmed FA, Hossain GM, Chen CH, Lee KH, Kashiwada Y..  (2022)  Tigliane-Type Diterpene Esters from the Fruits of Shirakiopsis indica and Their Anti-HIV Activity.,  85  (11.0): [PMID:36378070] [10.1021/acs.jnatprod.2c00752]

Source