ID: ALA5288349

Max Phase: Preclinical

Molecular Formula: C36H50O3

Molecular Weight: 530.79

Representations

Canonical SMILES:  C=C(C)[C@@H]1CC[C@]2(C(=O)O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccccc6O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12

Standard InChI:  InChI=1S/C36H50O3/c1-22(2)23-14-19-36(31(38)39)21-20-34(6)26(30(23)36)12-13-29-33(5)17-15-25(24-10-8-9-11-27(24)37)32(3,4)28(33)16-18-35(29,34)7/h8-11,15,23,26,28-30,37H,1,12-14,16-21H2,2-7H3,(H,38,39)/t23-,26+,28-,29+,30+,33-,34+,35+,36-/m0/s1

Standard InChI Key:  ATHSRNOEAZIXFA-CCSYMGPDSA-N

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

Properties

Molecular Weight: 530.79

Molecular Weight (Monoisotopic): 530.3760

AlogP: 9.13

#Rotatable Bonds: 3

Polar Surface Area: 57.53

Molecular Species: ACID

HBA: 2

HBD: 2

#RO5 Violations: 2

HBA (Lipinski): 3

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 4.78

CX Basic pKa:

CX LogP: 8.72

CX LogD: 6.14

Aromatic Rings: 1

Heavy Atoms: 39

QED Weighted: 0.38

Np Likeness Score: 2.57

References

1. Borková L, Frydrych I, Vránová B, Jakubcová N, Lišková B, Gurská S, Džubák P, Pavliš P, Hajdúch M, Urban M..  (2022)  Lupane derivatives containing various aryl substituents in the position 3 have selective cytostatic effect in leukemic cancer cells including resistant phenotypes.,  244  [PMID:36283179] [10.1016/j.ejmech.2022.114850]

Source

Source(1):

• Scientific Literature