(3alpha)-3-[(trans-2,5-Dimethyl-4-{[2-(trifluoromethyl)phenyl]sulfonyl}piperazin-1-yl)methyl]-17-methoxyandrostan-3-ol

ID: ALA4462874

PubChem CID: 155529611

Max Phase: Preclinical

Molecular Formula: C34H51F3N2O4S

Molecular Weight: 640.85

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  CO[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@](O)(CN5CC(C)N(S(=O)(=O)c6ccccc6C(F)(F)F)CC5C)CC[C@]4(C)[C@H]3CC[C@]12C

Standard InChI:  InChI=1S/C34H51F3N2O4S/c1-22-20-39(44(41,42)29-9-7-6-8-28(29)34(35,36)37)23(2)19-38(22)21-33(40)17-16-31(3)24(18-33)10-11-25-26-12-13-30(43-5)32(26,4)15-14-27(25)31/h6-9,22-27,30,40H,10-21H2,1-5H3/t22?,23?,24-,25-,26-,27-,30-,31-,32-,33+/m0/s1

Standard InChI Key:  ROCSLJHPNWPYCO-KEBXQEJFSA-N

Molfile:  

 
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M  END

Alternative Forms

1. Parent:

   

   ALA4462874

   ---

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: 640.85

Molecular Weight (Monoisotopic): 640.3522

AlogP: 6.58

#Rotatable Bonds: 5

Polar Surface Area: 70.08

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: 7.37

CX LogP: 6.18

CX LogD: 5.90

Aromatic Rings: 1

Heavy Atoms: 44

QED Weighted: 0.39

Np Likeness Score: 0.49

References

1. Cortés-Benítez F, Roy J, Perreault M, Maltais R, Poirier D..  (2019)  A- and D-Ring Structural Modifications of an Androsterone Derivative Inhibiting 17β-Hydroxysteroid Dehydrogenase Type 3: Chemical Synthesis and Structure-Activity Relationships.,  62  (15): [PMID:31268309] [10.1021/acs.jmedchem.9b00624]

Source

Source(1):

• Scientific Literature