Ergosta-7,22-diene-3-one

ID: ALA5191846

Chembl Id: CHEMBL5191846

Cas Number: 32507-77-0

PubChem CID: 101449383

Max Phase: Preclinical

Molecular Formula: C28H44O

Molecular Weight: 396.66

Names and Identifiers

Canonical SMILES:  CC(C)[C@@H](C)/C=C/[C@@H](C)[C@H]1CC[C@H]2C3=CC[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

Standard InChI:  InChI=1S/C28H44O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-8,10,18-21,24-26H,9,11-17H2,1-6H3/b8-7+/t19-,20+,21-,24+,25-,26-,27-,28+/m0/s1

Standard InChI Key:  AHWOEMBXZXGDBQ-LLSCCSQYSA-N

Alternative Forms

1. Parent:

   

   ALA5191846

   (5S,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-1,2,4,5,6,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

Molecule Features

Natural Product: No

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: 396.66

Molecular Weight (Monoisotopic): 396.3392

AlogP: 7.62

#Rotatable Bonds: 4

Polar Surface Area: 17.07

Molecular Species: NEUTRAL

HBA: 1

HBD: 0

#RO5 Violations: 1

HBA (Lipinski): 1

HBD (Lipinski): 0

#RO5 Violations (Lipinski): 1

CX Acidic pKa:

CX Basic pKa:

CX LogP: 7.25

CX LogD: 7.25

Aromatic Rings: 0

Heavy Atoms: 29

QED Weighted: 0.45

Np Likeness Score: 2.84

References

1. Yazdani M, Béni Z, Dékány M, Szemerédi N, Spengler G, Hohmann J, Ványolós A..  (2022)  Triterpenes from Pholiota populnea as Cytotoxic Agents and Chemosensitizers to Overcome Multidrug Resistance of Cancer Cells.,  85  (4.0): [PMID:35293752] [10.1021/acs.jnatprod.1c01024]

Source

Source(1):

• Scientific Literature