ID: ALA3358316

Max Phase: Preclinical

Molecular Formula: C23H35ClO3

Molecular Weight: 394.98

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)C1=CC2=CC[C@@H]3[C@](C)(CCC[C@@]3(C)C(=O)OCC(O)CCl)[C@H]2CC1

Standard InChI:  InChI=1S/C23H35ClO3/c1-15(2)16-6-8-19-17(12-16)7-9-20-22(19,3)10-5-11-23(20,4)21(26)27-14-18(25)13-24/h7,12,15,18-20,25H,5-6,8-11,13-14H2,1-4H3/t18?,19-,20+,22+,23+/m0/s1

Standard InChI Key:  CVQBKJYQVURQSY-MWJPAGEPSA-N

Associated Targets(non-human)

Trametes versicolor 86 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Gloeophyllum trabeum 56 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: 394.98Molecular Weight (Monoisotopic): 394.2275AlogP: 5.26#Rotatable Bonds: 5
Polar Surface Area: 46.53Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.57CX Basic pKa: CX LogP: 5.13CX LogD: 5.13
Aromatic Rings: 0Heavy Atoms: 27QED Weighted: 0.51Np Likeness Score: 2.53

References

1. Wang H, Nguyen TT, Li S, Liang T, Zhang Y, Li J..  (2015)  Quantitative structure-activity relationship of antifungal activity of rosin derivatives.,  25  (2): [PMID:25466709] [10.1016/j.bmcl.2014.11.034]

Source