4-{2-[2-(4-Chloro-phenyl)-ethyl]-2-imidazol-1-ylmethyl-[1,3]dioxolan-4-ylmethylsulfanyl}-phenylamine

ID: ALA305220

PubChem CID: 25142015

Max Phase: Preclinical

Molecular Formula: C22H24ClN3O2S

Molecular Weight: 429.97

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  Nc1ccc(SC[C@H]2CO[C@@](CCc3ccc(Cl)cc3)(Cn3ccnc3)O2)cc1

Standard InChI:  InChI=1S/C22H24ClN3O2S/c23-18-3-1-17(2-4-18)9-10-22(15-26-12-11-25-16-26)27-13-20(28-22)14-29-21-7-5-19(24)6-8-21/h1-8,11-12,16,20H,9-10,13-15,24H2/t20-,22-/m1/s1

Standard InChI Key:  VYNIUBZKEWJOJP-IFMALSPDSA-N

Molfile:  

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   -3.9978   -2.2972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0000   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.3084   -4.8243    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8003   -4.9871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4079   -6.3586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8994   -6.5183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7834   -5.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1759   -3.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6845   -3.7753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.9766   -5.4342    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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  1 14  1  6
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 19 20  2  0
  3 21  1  1
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 26 29  1  0
M  END

Alternative Forms

1. Parent:

   

   ALA305220

   4-{2-[2-(4-Chloro-phenyl)-ethyl]-2-imidazol-1-ylmethyl-[1,3]dioxolan-4-ylmethylsulfanyl}-phenylamine

2. Alternative Forms:

   

   ALA305220

   4-[[(2R,4R)-2-[2-(4-chlorophenyl)ethyl]-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methylsulfanyl]aniline;dihydrochloride

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 429.97

Molecular Weight (Monoisotopic): 429.1278

AlogP: 4.66

#Rotatable Bonds: 8

Polar Surface Area: 62.30

Molecular Species: NEUTRAL

HBA: 6

HBD: 1

#RO5 Violations: ┄

HBA (Lipinski): 5

HBD (Lipinski): 2

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: ┄

CX Basic pKa: 6.43

CX LogP: 4.61

CX LogD: 4.57

Aromatic Rings: 3

Heavy Atoms: 29

QED Weighted: 0.42

Np Likeness Score: -0.60

References

1. Walker KA, Kertesz DJ, Rotstein DM, Swinney DC, Berry PW, So OY, Webb AS, Watson DM, Mak AY, Burton PM..  (1993)  Selective inhibition of mammalian lanosterol 14 alpha-demethylase: a possible strategy for cholesterol lowering.,  36  (15): [PMID:8340925] [10.1021/jm00067a022]

2. Vlahakis JZ, Kinobe RT, Bowers RJ, Brien JF, Nakatsu K, Szarek WA..  (2005)  Synthesis and evaluation of azalanstat analogues as heme oxygenase inhibitors.,  15  (5): [PMID:15713406] [10.1016/j.bmcl.2004.12.075]

Source

Source(1):

• Scientific Literature