3-[(S)-3-oxo-3-[4-(piperidine-4-carbonyl)-piperazin-1-yl]-2-(2,4,6-triisopropyl-benzenesulfonylamino)-propyl]-benzamidine

ID: ALA379186

Chembl Id: CHEMBL379186

PubChem CID: 11607091

Max Phase: Preclinical

Molecular Formula: C35H52N6O4S

Molecular Weight: 652.91

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CC(C)c1cc(C(C)C)c(S(=O)(=O)N[C@@H](Cc2cccc(C(=N)N)c2)C(=O)N2CCN(C(=O)C3CCNCC3)CC2)c(C(C)C)c1

Standard InChI:  InChI=1S/C35H52N6O4S/c1-22(2)28-20-29(23(3)4)32(30(21-28)24(5)6)46(44,45)39-31(19-25-8-7-9-27(18-25)33(36)37)35(43)41-16-14-40(15-17-41)34(42)26-10-12-38-13-11-26/h7-9,18,20-24,26,31,38-39H,10-17,19H2,1-6H3,(H3,36,37)/t31-/m0/s1

Standard InChI Key:  XKXAXFJNQDWDNX-HKBQPEDESA-N

Alternative Forms

1. Parent:

   

   ALA379186

   3-Amidinophenylalanine deriv., 30

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

Calculated Properties

Molecular Weight: 652.91

Molecular Weight (Monoisotopic): 652.3771

AlogP: 3.90

#Rotatable Bonds: 11

Polar Surface Area: 148.69

Molecular Species: BASE

HBA: 6

HBD: 4

#RO5 Violations: 1

HBA (Lipinski): 10

HBD (Lipinski): 5

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 10.68

CX Basic pKa: 11.53

CX LogP: 3.51

CX LogD: -1.03

Aromatic Rings: 2

Heavy Atoms: 46

QED Weighted: 0.21

Np Likeness Score: -0.74

References

1. Steinmetzer T, Schweinitz A, Stürzebecher A, Dönnecke D, Uhland K, Schuster O, Steinmetzer P, Müller F, Friedrich R, Than ME, Bode W, Stürzebecher J..  (2006)  Secondary amides of sulfonylated 3-amidinophenylalanine. New potent and selective inhibitors of matriptase.,  49  (14): [PMID:16821772] [10.1021/jm051272l]

2. Franco FM, Jones DE, Harris PK, Han Z, Wildman SA, Jarvis CM, Janetka JW..  (2015)  Structure-based discovery of small molecule hepsin and HGFA protease inhibitors: Evaluation of potency and selectivity derived from distinct binding pockets.,  23  (10): [PMID:25882520] [10.1016/j.bmc.2015.03.072]

3. Damalanka VC, Wildman SA, Janetka JW..  (2019)  Piperidine carbamate peptidomimetic inhibitors of the serine proteases HGFA, matriptase and hepsin.,  10  (9): [PMID:31803403] [10.1039/C9MD00234K]

Source

Source(1):

• Scientific Literature