1-(4,5-Bis(4-isopropylphenyl)thiophen-2-yl)-N-(piperidin-4-ylmethyl)methanamine

ID: ALA4483638

PubChem CID: 155540348

Max Phase: Preclinical

Molecular Formula: C29H38N2S

Molecular Weight: 446.70

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  CC(C)c1ccc(-c2cc(CNCC3CCNCC3)sc2-c2ccc(C(C)C)cc2)cc1

Standard InChI:  InChI=1S/C29H38N2S/c1-20(2)23-5-9-25(10-6-23)28-17-27(19-31-18-22-13-15-30-16-14-22)32-29(28)26-11-7-24(8-12-26)21(3)4/h5-12,17,20-22,30-31H,13-16,18-19H2,1-4H3

Standard InChI Key:  UOUIHPZVDAINIH-UHFFFAOYSA-N

Molfile:  

 
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M  END

Alternative Forms

1. Parent:

   

   ALA4483638

   ---

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: 446.70

Molecular Weight (Monoisotopic): 446.2756

AlogP: 7.42

#Rotatable Bonds: 8

Polar Surface Area: 24.06

Molecular Species: BASE

HBA: 3

HBD: 2

#RO5 Violations: 1

HBA (Lipinski): 2

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 1

CX Acidic pKa: ┄

CX Basic pKa: 10.53

CX LogP: 7.33

CX LogD: 2.02

Aromatic Rings: 3

Heavy Atoms: 32

QED Weighted: 0.38

Np Likeness Score: -0.34

References

1. Wu F, Hua Y, Kaochar S, Nie S, Lin YL, Yao Y, Wu J, Wu X, Fu X, Schiff R, Davis CM, Robertson M, Ehli EA, Coarfa C, Mitsiades N, Song Y..  (2020)  Discovery, Structure-Activity Relationship, and Biological Activity of Histone-Competitive Inhibitors of Histone Acetyltransferases P300/CBP.,  63  (9): [PMID:32314924] [10.1021/acs.jmedchem.9b02164]

Source

Source(1):

• Scientific Literature