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5-chloro-N-(4-(5-(4-fluoro-3-(trifluoromethyl)phenylsulfonamido)benzo[d]oxazol-2-yl)phenyl)thiophene-2-sulfonamide ID: ALA4531228
PubChem CID: 155546030
Max Phase: Preclinical
Molecular Formula: C24H14ClF4N3O5S3
Molecular Weight: 632.04
Molecule Type: Unknown
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: O=S(=O)(Nc1ccc2oc(-c3ccc(NS(=O)(=O)c4ccc(Cl)s4)cc3)nc2c1)c1ccc(F)c(C(F)(F)F)c1
Standard InChI: InChI=1S/C24H14ClF4N3O5S3/c25-21-9-10-22(38-21)40(35,36)31-14-3-1-13(2-4-14)23-30-19-11-15(5-8-20(19)37-23)32-39(33,34)16-6-7-18(26)17(12-16)24(27,28)29/h1-12,31-32H
Standard InChI Key: HGFBPMWHZSDSBS-UHFFFAOYSA-N
Molfile:
RDKit 2D
40 44 0 0 0 0 0 0 0 0999 V2000
12.1960 -3.6113 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
12.2001 -2.7941 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
11.4903 -3.1992 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.0158 -1.8201 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.4285 -2.5300 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
4.8369 -1.8176 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.8469 -1.7128 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.8457 -2.5323 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5538 -2.9413 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5520 -1.3039 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1377 -2.9403 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.7216 -2.9432 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.2606 -1.7092 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.2654 -2.5278 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0454 -2.7762 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
8.5228 -2.1111 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0377 -1.4517 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
9.3400 -2.1063 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.7501 -2.8127 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.5666 -2.8082 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.9718 -2.0976 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.5546 -1.3900 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.7396 -1.3979 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.7890 -2.0917 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
13.0173 -2.7941 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.5013 -3.4525 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
14.2785 -3.2000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.2785 -2.3828 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
13.5012 -2.1304 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
14.9396 -3.6804 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0
3.0106 -2.5360 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3042 -2.9486 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3082 -3.7682 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.0245 -4.1736 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.7280 -3.7587 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5945 -2.5435 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5905 -1.7263 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
0.8888 -2.9555 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
0.8832 -2.1338 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
1.6033 -4.1816 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
2 1 2 0
3 2 2 0
5 4 2 0
6 5 2 0
7 8 2 0
8 9 1 0
9 14 2 0
13 10 2 0
10 7 1 0
8 11 1 0
11 5 1 0
5 12 1 0
13 14 1 0
14 15 1 0
15 16 2 0
16 17 1 0
17 13 1 0
16 18 1 0
18 19 2 0
19 20 1 0
20 21 2 0
21 22 1 0
22 23 2 0
23 18 1 0
21 24 1 0
24 2 1 0
2 25 1 0
25 26 1 0
26 27 1 0
27 28 2 0
28 29 1 0
29 25 2 0
27 30 1 0
12 31 2 0
31 32 1 0
32 33 2 0
33 34 1 0
34 35 2 0
35 12 1 0
32 36 1 0
36 37 1 0
36 38 1 0
36 39 1 0
33 40 1 0
M END Associated Targets(Human) Associated Targets(non-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: 632.04Molecular Weight (Monoisotopic): 630.9720AlogP: 6.97#Rotatable Bonds: 7Polar Surface Area: 118.37Molecular Species: ACIDHBA: 7HBD: 2#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 2CX Acidic pKa: 6.11CX Basic pKa: 0.82CX LogP: 6.06CX LogD: 5.09Aromatic Rings: 5Heavy Atoms: 40QED Weighted: 0.19Np Likeness Score: -2.16
References 1. Washburn A, Abdeen S, Ovechkina Y, Ray AM, Stevens M, Chitre S, Sivinski J, Park Y, Johnson J, Hoang QQ, Chapman E, Parish T, Johnson SM.. (2019) Dual-targeting GroEL/ES chaperonin and protein tyrosine phosphatase B (PtpB) inhibitors: A polypharmacology strategy for treating Mycobacterium tuberculosis infections., 29 (13): [PMID:31047750 ] [10.1016/j.bmcl.2019.04.034 ]