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(R,E)-3-(3-methoxyphenyl)-N-(3-phenyl-2-(4-(trifluoromethyl)phenylsulfonamido)propyl)acrylamide ID: ALA5282208
Max Phase: Preclinical
Molecular Formula: C26H25F3N2O4S
Molecular Weight: 518.56
Associated Items:
Names and Identifiers Canonical SMILES: COc1cccc(/C=C/C(=O)NC[C@@H](Cc2ccccc2)NS(=O)(=O)c2ccc(C(F)(F)F)cc2)c1
Standard InChI: InChI=1S/C26H25F3N2O4S/c1-35-23-9-5-8-20(17-23)10-15-25(32)30-18-22(16-19-6-3-2-4-7-19)31-36(33,34)24-13-11-21(12-14-24)26(27,28)29/h2-15,17,22,31H,16,18H2,1H3,(H,30,32)/b15-10+/t22-/m1/s1
Standard InChI Key: YQXARSVRDPJIEQ-RCJYHZQCSA-N
Molfile:
RDKit 2D
36 38 0 0 0 0 0 0 0 0999 V2000
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-3.1570 -3.4187 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.5714 -3.9995 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
-3.9821 -0.1139 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.1570 -0.1180 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
-3.5660 0.5984 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.4403 1.1153 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.7257 1.5279 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1548 1.5279 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4403 0.2901 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-1.0109 1.1153 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-0.2964 1.5279 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4179 1.1153 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.2964 2.3530 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.1325 1.5279 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.8471 1.1153 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.8449 0.2890 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5588 -0.1232 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.2744 0.2891 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.2717 1.1186 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5574 1.5274 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1548 2.3530 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4368 2.7617 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4365 3.5860 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1516 3.9995 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.8684 3.5824 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.8653 2.7595 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1548 -0.9473 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.8727 -1.3562 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.8731 -2.1805 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1581 -2.5940 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4411 -2.1769 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4443 -1.3539 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9821 1.5300 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.9792 2.3551 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.8709 -3.8326 0.0000 F 0 0 0 0 0 0 0 0 0 0 0 0
2 1 1 0
3 2 1 0
5 4 2 0
6 5 2 0
7 8 1 0
7 9 1 6
7 10 1 0
10 5 1 0
8 11 1 0
11 12 1 0
12 13 1 0
12 14 2 0
13 15 2 0
15 16 1 0
16 17 2 0
17 18 1 0
18 19 2 0
19 20 1 0
20 21 2 0
21 16 1 0
9 22 1 0
22 23 2 0
23 24 1 0
24 25 2 0
25 26 1 0
26 27 2 0
27 22 1 0
5 28 1 0
28 29 2 0
29 30 1 0
30 31 2 0
31 2 1 0
31 32 1 0
32 33 2 0
33 28 1 0
20 34 1 0
34 35 1 0
2 36 1 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: 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: 518.56Molecular Weight (Monoisotopic): 518.1487AlogP: 4.43#Rotatable Bonds: 10Polar Surface Area: 84.50Molecular Species: NEUTRALHBA: 4HBD: 2#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: 10.11CX Basic pKa: ┄CX LogP: 4.98CX LogD: 4.98Aromatic Rings: 3Heavy Atoms: 36QED Weighted: 0.39Np Likeness Score: -0.87
References 1. Huang H, Zhang Y, Xu X, Liu Y, Zhao J, Ma L, Lei J, Ge W, Li N, Ma E, Li Y, Yuan L.. (2023) Design and synthesis of dual cathepsin L and S inhibitors and antimetastatic activity evaluation in pancreatic cancer cells., 80 [PMID:36427655 ] [10.1016/j.bmcl.2022.129087 ]