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N-Hydroxysuccinyl-L-phenylalanylglycyl[(2,4,6-Trimethylbenzoyl)oxy)methyl ketone ID: ALA53410
PubChem CID: 44297707
Max Phase: Preclinical
Molecular Formula: C31H34N2O6
Molecular Weight: 530.62
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: Cc1cc(C)c(C(=O)OCC(=O)[C@@H](C)NC(=O)[C@H](Cc2ccccc2)NC(=O)OCc2ccccc2)c(C)c1
Standard InChI: InChI=1S/C31H34N2O6/c1-20-15-21(2)28(22(3)16-20)30(36)38-19-27(34)23(4)32-29(35)26(17-24-11-7-5-8-12-24)33-31(37)39-18-25-13-9-6-10-14-25/h5-16,23,26H,17-19H2,1-4H3,(H,32,35)(H,33,37)/t23-,26+/m1/s1
Standard InChI Key: OFCOJPYLXMKAGH-BVAGGSTKSA-N
Molfile:
RDKit 2D
39 41 0 0 1 0 0 0 0 0999 V2000
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14.2917 -3.7917 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.9958 -1.5375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1917 -3.0125 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-0.0083 -2.9917 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.6917 -3.7833 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5917 -3.0000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2917 -3.7458 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
7.7917 -3.0208 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4917 -3.7667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.3917 -3.0292 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
14.2958 -0.7917 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
15.5917 -3.0417 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.8875 -4.9583 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
9.0917 -3.7750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5958 -1.5000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.0042 -1.7917 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
11.6875 -4.9833 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
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6.4875 -4.9667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
16.6333 -0.9458 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.1917 -1.5042 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9000 0.7500 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.9125 -5.2292 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.2083 -2.9750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2000 1.4958 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4917 -0.7583 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.5042 -3.7250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.2125 -5.9750 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.5042 -5.2250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5000 0.7417 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 7 1 0
3 2 2 0
4 2 1 0
5 1 1 0
6 9 1 0
7 12 1 0
8 1 1 0
9 8 1 0
10 11 1 0
11 5 1 0
12 16 1 0
13 4 2 0
14 3 1 0
15 1 2 0
16 10 1 0
8 17 1 1
18 6 2 0
19 7 2 0
20 13 1 0
21 6 1 0
22 10 2 0
23 21 1 0
24 17 1 0
25 3 1 0
26 4 1 0
27 23 1 0
11 28 1 1
29 20 1 0
30 24 1 0
31 24 2 0
32 27 1 0
33 27 2 0
34 31 1 0
35 30 2 0
36 33 1 0
37 32 2 0
38 37 1 0
39 35 1 0
39 34 2 0
38 36 2 0
20 14 2 0
M END Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: 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: 530.62Molecular Weight (Monoisotopic): 530.2417AlogP: 4.38#Rotatable Bonds: 11Polar Surface Area: 110.80Molecular Species: NEUTRALHBA: 6HBD: 2#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: 12.49CX Basic pKa: ┄CX LogP: 6.25CX LogD: 6.25Aromatic Rings: 3Heavy Atoms: 39QED Weighted: 0.36Np Likeness Score: -0.30
References 1. Wagner BM, Smith RA, Coles PJ, Copp LJ, Ernest MJ, Krantz A.. (1994) In vivo inhibition of cathepsin B by peptidyl (acyloxy)methyl ketones., 37 (12): [PMID:8021922 ] [10.1021/jm00038a012 ]