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1-(4,5-Bis(4-(tert-butyl)phenyl)thiazol-2-yl)-N-(piperidin-4-ylmethyl)methanamine ID: ALA4535532
PubChem CID: 155547999
Max Phase: Preclinical
Molecular Formula: C30H41N3S
Molecular Weight: 475.75
Molecule Type: Unknown
Associated Items:
Names and Identifiers Canonical SMILES: CC(C)(C)c1ccc(-c2nc(CNCC3CCNCC3)sc2-c2ccc(C(C)(C)C)cc2)cc1
Standard InChI: InChI=1S/C30H41N3S/c1-29(2,3)24-11-7-22(8-12-24)27-28(23-9-13-25(14-10-23)30(4,5)6)34-26(33-27)20-32-19-21-15-17-31-18-16-21/h7-14,21,31-32H,15-20H2,1-6H3
Standard InChI Key: AEAIJIUTWWOCDU-UHFFFAOYSA-N
Molfile:
RDKit 2D
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18.8404 -4.3253 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
18.5879 -5.1066 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
19.2490 -5.5912 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
19.9142 -5.1066 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
20.6955 -5.3591 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
21.3069 -4.8123 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
22.0883 -5.0648 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
18.3579 -3.6646 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
18.6961 -2.9134 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
18.2124 -2.2527 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
17.3946 -2.3378 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
17.0629 -3.0934 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
17.5445 -3.7509 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
17.8101 -5.3582 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
17.1988 -4.8096 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.4180 -5.0616 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.2475 -5.8658 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.8638 -6.4176 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
17.6421 -6.1586 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.9129 -1.6776 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
17.2438 -0.9304 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.1004 -1.7647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.4965 -0.9658 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.4707 -6.1196 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.8625 -5.5737 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.3021 -6.9192 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.6764 -6.3270 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
22.6947 -4.5171 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
23.4723 -4.7684 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
22.5235 -3.7180 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
23.1300 -3.1703 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
23.9076 -3.4216 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
24.0787 -4.2206 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
9 10 2 0
10 11 1 0
11 12 2 0
12 13 1 0
13 14 2 0
14 9 1 0
2 9 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
3 15 1 0
12 21 1 0
21 22 1 0
21 23 1 0
21 24 1 0
18 25 1 0
25 26 1 0
25 27 1 0
25 28 1 0
8 29 1 0
29 30 1 0
29 31 1 0
31 32 1 0
30 34 1 0
32 33 1 0
33 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: 475.75Molecular Weight (Monoisotopic): 475.3021AlogP: 7.16#Rotatable Bonds: 6Polar Surface Area: 36.95Molecular Species: BASEHBA: 4HBD: 2#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 10.37CX LogP: 7.14CX LogD: 2.84Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.40Np Likeness Score: -0.81
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 ]