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1-(4,5-Bis(4-(tert-butyl)phenyl)thiophen-2-yl)-N-(piperidin-4-ylmethyl)methanamine ID: ALA4474132
PubChem CID: 155536635
Max Phase: Preclinical
Molecular Formula: C31H42N2S
Molecular Weight: 474.76
Molecule Type: Unknown
Associated Items:
Names and Identifiers Canonical SMILES: CC(C)(C)c1ccc(-c2cc(CNCC3CCNCC3)sc2-c2ccc(C(C)(C)C)cc2)cc1
Standard InChI: InChI=1S/C31H42N2S/c1-30(2,3)25-11-7-23(8-12-25)28-19-27(21-33-20-22-15-17-32-18-16-22)34-29(28)24-9-13-26(14-10-24)31(4,5)6/h7-14,19,22,32-33H,15-18,20-21H2,1-6H3
Standard InChI Key: WEJUPZWNBLRNHH-UHFFFAOYSA-N
Molfile:
RDKit 2D
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33.2692 -4.9114 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
33.0166 -5.6927 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
33.6778 -6.1772 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
34.3430 -5.6927 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
35.1243 -5.9452 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
35.7357 -5.3984 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
36.5170 -5.6509 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
37.1285 -5.1000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
37.9058 -5.3620 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
38.5117 -4.8149 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
38.3458 -4.0102 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
37.5642 -3.7556 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
36.9484 -4.3014 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.7867 -4.2506 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
33.1249 -3.4995 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.6412 -2.8388 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.8234 -2.9238 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.4917 -3.6794 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.9733 -4.3370 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.2389 -5.9443 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.6275 -5.3957 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.8468 -5.6476 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.6763 -6.4518 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.2926 -7.0037 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.0709 -6.7447 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.3417 -2.2637 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.6726 -1.5165 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.5292 -2.3508 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.9253 -1.5518 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.8995 -6.7056 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.2913 -6.1598 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.7309 -7.5052 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.1052 -6.9131 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
2 3 2 0
3 4 1 0
4 5 1 0
5 1 2 0
5 6 1 0
6 7 1 0
7 8 1 0
8 9 1 0
9 10 1 0
9 14 1 0
10 11 1 0
11 12 1 0
12 13 1 0
13 14 1 0
15 16 2 0
16 17 1 0
17 18 2 0
18 19 1 0
19 20 2 0
20 15 1 0
2 15 1 0
21 22 2 0
22 23 1 0
23 24 2 0
24 25 1 0
25 26 2 0
26 21 1 0
3 21 1 0
18 27 1 0
27 28 1 0
27 29 1 0
27 30 1 0
24 31 1 0
31 32 1 0
31 33 1 0
31 34 1 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 474.76Molecular Weight (Monoisotopic): 474.3069AlogP: 7.77#Rotatable Bonds: 6Polar Surface Area: 24.06Molecular Species: BASEHBA: 3HBD: 2#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 10.53CX LogP: 7.93CX LogD: 2.62Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.38Np Likeness Score: -0.46
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 ]