ID: ALA4536219

Max Phase: Preclinical

Molecular Formula: C29H40O8

Molecular Weight: 516.63

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C=CC(=C)CCC1(C)C(C)CC(=O)C23C(=C[C@H](OC(=O)[C@@H](C)CC)CC12)[C@@H](OC(C)=O)O[C@H]3OC(C)=O

Standard InChI:  InChI=1S/C29H40O8/c1-9-16(3)11-12-28(8)18(5)13-24(32)29-22(26(34-19(6)30)37-27(29)35-20(7)31)14-21(15-23(28)29)36-25(33)17(4)10-2/h9,14,17-18,21,23,26-27H,1,3,10-13,15H2,2,4-8H3/t17-,18?,21-,23?,26-,27+,28?,29?/m0/s1

Standard InChI Key:  QVIWRQOHOJKWLQ-PMHOREOUSA-N

Associated Targets(Human)

A673 619 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Hep293TT 35 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: 516.63Molecular Weight (Monoisotopic): 516.2723AlogP: 4.82#Rotatable Bonds: 9
Polar Surface Area: 105.20Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.12CX LogD: 5.12
Aromatic Rings: 0Heavy Atoms: 37QED Weighted: 0.19Np Likeness Score: 2.89

References

1. Cai S, Risinger AL, Petersen CL, Grkovic T, O'Keefe BR, Mooberry SL, Cichewicz RH..  (2019)  Anacolosins A-F and Corymbulosins X and Y, Clerodane Diterpenes from Anacolosa clarkii Exhibiting Cytotoxicity toward Pediatric Cancer Cell Lines.,  82  (4): [PMID:30830773] [10.1021/acs.jnatprod.8b01015]

Source