2alpha,3beta-Diacetyloxy-olean-12-en-28-oic acid ethylphenylamide

ID: ALA4437507

Chembl Id: CHEMBL4437507

PubChem CID: 155512670

Max Phase: Preclinical

Molecular Formula: C42H61NO5

Molecular Weight: 659.95

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  CC(=O)O[C@@H]1C[C@]2(C)[C@H]3CC=C4[C@@H]5CC(C)(C)CC[C@]5(C(=O)NCCc5ccccc5)CC[C@@]4(C)[C@]3(C)CC[C@H]2C(C)(C)[C@H]1OC(C)=O

Standard InChI:  InChI=1S/C42H61NO5/c1-27(44)47-32-26-39(7)33(38(5,6)35(32)48-28(2)45)17-19-41(9)34(39)16-15-30-31-25-37(3,4)20-22-42(31,23-21-40(30,41)8)36(46)43-24-18-29-13-11-10-12-14-29/h10-15,31-35H,16-26H2,1-9H3,(H,43,46)/t31-,32+,33-,34+,35-,39-,40+,41+,42-/m0/s1

Standard InChI Key:  QUTUAMKTEZOXJD-DARIJYBNSA-N

Alternative Forms

1. Parent:

   

   ALA4437507

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 659.95

Molecular Weight (Monoisotopic): 659.4550

AlogP: 8.62

#Rotatable Bonds: 6

Polar Surface Area: 81.70

Molecular Species: NEUTRAL

HBA: 5

HBD: 1

#RO5 Violations: 2

HBA (Lipinski): 6

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 2

CX Acidic pKa: ┄

CX Basic pKa: 0.49

CX LogP: 7.83

CX LogD: 7.83

Aromatic Rings: 1

Heavy Atoms: 48

QED Weighted: 0.24

Np Likeness Score: 2.20

References

1. Sommerwerk S, Heller L, Kuhfs J, Csuk R..  (2016)  Urea derivates of ursolic, oleanolic and maslinic acid induce apoptosis and are selective cytotoxic for several human tumor cell lines.,  119  [PMID:27149037] [10.1016/j.ejmech.2016.04.051]

Source

Source(1):

• Scientific Literature