ID: ALA446908

Max Phase: Preclinical

Molecular Formula: C36H51N5O6S

Molecular Weight: 681.90

Molecule Type: Small molecule

Representations

Synonyms (1): KNI-10516
Synonyms from Alternative Forms(1):

Canonical SMILES:  CC(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)[C@H](O)C(=O)N1CSC(C)(C)[C@H]1C(=O)NCC(C)C)C(C)(C)C)c1ccccc1

Standard InChI:  InChI=1S/C36H51N5O6S/c1-22(2)20-37-33(46)30-36(7,8)48-21-41(30)34(47)28(43)26(19-24-15-11-9-12-16-24)39-32(45)29(35(4,5)6)40-31(44)27(38-23(3)42)25-17-13-10-14-18-25/h9-18,22,26-30,43H,19-21H2,1-8H3,(H,37,46)(H,38,42)(H,39,45)(H,40,44)/t26-,27-,28-,29+,30+/m0/s1

Standard InChI Key:  QYKYACJJBYHVHC-WQOITCGXSA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 681.90

Molecular Weight (Monoisotopic): 681.3560

AlogP: 2.94

#Rotatable Bonds: 13

Polar Surface Area: 156.94

Molecular Species: NEUTRAL

HBA: 7

HBD: 5

#RO5 Violations: 1

HBA (Lipinski): 11

HBD (Lipinski): 5

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 11.76

CX Basic pKa:

CX LogP: 2.73

CX LogD: 2.73

Aromatic Rings: 2

Heavy Atoms: 48

QED Weighted: 0.22

Np Likeness Score: 0.38

References

1. Zhang M, Nguyen JT, Kumada HO, Kimura T, Cheng M, Hayashi Y, Kiso Y..  (2008)  Locking the two ends of tetrapeptidic HTLV-I protease inhibitors inside the enzyme.,  16  (14): [PMID:18558491] [10.1016/j.bmc.2008.05.052]

2. Zhang M, Nguyen JT, Kumada HO, Kimura T, Cheng M, Hayashi Y, Kiso Y..  (2008)  Synthesis and activity of tetrapeptidic HTLV-I protease inhibitors possessing different P3-cap moieties.,  16  (10): [PMID:18400502] [10.1016/j.bmc.2008.03.055]

Source

Source(1):

• Scientific Literature