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NA ID: ALA4476472
PubChem CID: 118910215
Max Phase: Preclinical
Molecular Formula: C32H39ClN2O5S
Molecular Weight: 599.19
Molecule Type: Unknown
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: C[C@@H]1[C@@H](C)C/C=C/[C@H](O)[C@@H]2CC[C@H]2CN2C[C@@]3(CCCc4cc(Cl)ccc43)COc3ccc(cc32)C(=O)NS1(=O)=O
Standard InChI: InChI=1S/C32H39ClN2O5S/c1-20-5-3-7-29(36)26-11-8-24(26)17-35-18-32(14-4-6-22-15-25(33)10-12-27(22)32)19-40-30-13-9-23(16-28(30)35)31(37)34-41(38,39)21(20)2/h3,7,9-10,12-13,15-16,20-21,24,26,29,36H,4-6,8,11,14,17-19H2,1-2H3,(H,34,37)/b7-3+/t20-,21+,24-,26+,29-,32-/m0/s1
Standard InChI Key: VRSBISSEYLZZBN-ZYVWNYNNSA-N
Molfile:
RDKit 2D
43 48 0 0 0 0 0 0 0 0999 V2000
11.7790 -6.6208 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
10.9540 -6.6208 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
11.3665 -7.3352 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
5.2201 -7.0006 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6271 -6.2842 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4461 -6.1520 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
5.5306 -7.7699 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.3253 -8.0060 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.4985 -4.9374 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9286 -5.7643 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.9257 -4.9337 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2103 -4.5247 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2122 -6.1776 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.4942 -5.7662 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.7829 -6.1800 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.7833 -7.0068 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.5012 -7.4182 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6796 -5.3608 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.4816 -5.1673 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.1832 -5.5996 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6136 -4.8958 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.9080 -4.4636 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.0569 -6.7039 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.0038 -7.5302 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.6919 -7.9875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.4334 -7.6195 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.4827 -6.7898 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7939 -6.3363 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.2202 -6.4202 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.9092 -6.8741 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
9.2689 -5.5966 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.6469 -4.1014 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.7029 -3.2783 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
9.3318 -4.5613 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.0726 -4.1982 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.7575 -4.6581 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.6878 -5.4767 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.3660 -5.9434 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.8737 -5.6264 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.1109 -5.5885 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2079 -3.6997 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0
7.3166 -3.8749 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
7.2624 -5.9625 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
2 1 2 0
3 2 2 0
4 5 1 0
5 6 1 0
4 7 1 0
6 23 1 0
7 8 1 0
8 24 1 0
9 14 2 0
13 10 2 0
10 11 1 0
11 12 2 0
12 9 1 0
13 14 1 0
4 13 1 1
14 15 1 0
15 16 1 0
16 17 1 0
17 4 1 0
6 18 1 0
18 19 1 0
19 20 1 0
20 21 1 0
22 21 1 0
22 19 1 0
23 24 2 0
24 25 1 0
25 26 2 0
26 27 1 0
27 28 2 0
28 23 1 0
27 29 1 0
29 30 1 0
29 31 2 0
22 32 1 0
32 33 1 1
32 34 1 0
34 35 2 0
35 36 1 0
36 37 1 0
37 38 1 0
37 39 1 1
38 2 1 0
38 40 1 1
30 2 1 0
12 41 1 0
22 42 1 1
19 43 1 6
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: 599.19Molecular Weight (Monoisotopic): 598.2268AlogP: 5.24#Rotatable Bonds: ┄Polar Surface Area: 95.94Molecular Species: ACIDHBA: 6HBD: 2#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 2CX Acidic pKa: 4.28CX Basic pKa: 3.63CX LogP: 5.31CX LogD: 4.80Aromatic Rings: 2Heavy Atoms: 41QED Weighted: 0.40Np Likeness Score: 0.42
References 1. Rescourio G, Gonzalez AZ, Jabri S, Belmontes B, Moody G, Whittington D, Huang X, Caenepeel S, Cardozo M, Cheng AC, Chow D, Dou H, Jones A, Kelly RC, Li Y, Lizarzaburu M, Lo MC, Mallari R, Meleza C, Rew Y, Simonovich S, Sun D, Turcotte S, Yan X, Wong SG, Yanez E, Zancanella M, Houze J, Medina JC, Hughes PE, Brown SP.. (2019) Discovery and in Vivo Evaluation of Macrocyclic Mcl-1 Inhibitors Featuring an α-Hydroxy Phenylacetic Acid Pharmacophore or Bioisostere., 62 (22): [PMID:31736296 ] [10.1021/acs.jmedchem.9b01310 ] 2. Li K.. (2021) Interdiction at a protein-protein interface: MCL-1 inhibitors for oncology., 32 [PMID:33253879 ] [10.1016/j.bmcl.2020.127717 ]