(+)-8-epi-puupehedione

ID: ALA5207547

Chembl Id: CHEMBL5207547

PubChem CID: 10042061

Max Phase: Preclinical

Molecular Formula: C21H26O3

Molecular Weight: 326.44

Names and Identifiers

Canonical SMILES:  CC1(C)CCC[C@]2(C)C3=CC4=CC(=O)C(=O)C=C4O[C@]3(C)CC[C@@H]12

Standard InChI:  InChI=1S/C21H26O3/c1-19(2)7-5-8-20(3)17(19)6-9-21(4)18(20)11-13-10-14(22)15(23)12-16(13)24-21/h10-12,17H,5-9H2,1-4H3/t17-,20-,21+/m0/s1

Standard InChI Key:  QLFLHSQZFRDPFM-DZFGPLHGSA-N

Alternative Forms

1. Parent:

   

   ALA5207547

   8-Epipuupehedione

Molecule Features

Natural Product: Yes

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 326.44

Molecular Weight (Monoisotopic): 326.1882

AlogP: 4.29

#Rotatable Bonds: 0

Polar Surface Area: 43.37

Molecular Species: NEUTRAL

HBA: 3

HBD: 0

#RO5 Violations: 0

HBA (Lipinski): 3

HBD (Lipinski): 0

#RO5 Violations (Lipinski): 0

CX Acidic pKa:

CX Basic pKa:

CX LogP: 4.11

CX LogD: 4.11

Aromatic Rings: 0

Heavy Atoms: 24

QED Weighted: 0.49

Np Likeness Score: 2.76

References

1. Wang X, Hu N, Kong W, Song B, Li S..  (2022)  Facile and divergent optimization of chromazonarol enabled the identification of simplified drimane meroterpenoids as novel pharmaceutical leads.,  227  [PMID:34653771] [10.1016/j.ejmech.2021.113912]

Source

Source(1):

• Scientific Literature