(R)-N-Hydroxy-4-(6-((1-(2-hydroxy-2-methylpropyl)azetidin-3-yl)buta-1,3-diyn-1-yl)-3-oxo-1H-pyrrolo[1,2-c]imidazol-2(3H)-yl)-2-methyl-2-(methylsulfonyl)butanamide

ID: ALA4539946

Chembl Id: CHEMBL4539946

PubChem CID: 155549688

Max Phase: Preclinical

Molecular Formula: C23H30N4O6S

Molecular Weight: 490.58

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  CC(C)(O)CN1CC(C#CC#Cc2cc3n(c2)C(=O)N(CC[C@](C)(C(=O)NO)S(C)(=O)=O)C3)C1

Standard InChI:  InChI=1S/C23H30N4O6S/c1-22(2,30)16-25-12-18(13-25)8-6-5-7-17-11-19-15-26(21(29)27(19)14-17)10-9-23(3,20(28)24-31)34(4,32)33/h11,14,18,30-31H,9-10,12-13,15-16H2,1-4H3,(H,24,28)/t23-/m1/s1

Standard InChI Key:  ZUJNGUNTPOGRRG-HSZRJFAPSA-N

Alternative Forms

1. Parent:

   

   ALA4539946

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Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 490.58

Molecular Weight (Monoisotopic): 490.1886

AlogP: 0.03

#Rotatable Bonds: 7

Polar Surface Area: 132.18

Molecular Species: NEUTRAL

HBA: 8

HBD: 3

#RO5 Violations: ┄

HBA (Lipinski): 10

HBD (Lipinski): 3

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 8.70

CX Basic pKa: 7.55

CX LogP: -1.04

CX LogD: -1.23

Aromatic Rings: 1

Heavy Atoms: 34

QED Weighted: 0.28

Np Likeness Score: 0.00

References

1. Panchaud P, Surivet JP, Diethelm S, Blumstein AC, Gauvin JC, Jacob L, Masse F, Mathieu G, Mirre A, Schmitt C, Enderlin-Paput M, Lange R, Gnerre C, Seeland S, Herrmann C, Locher HH, Seiler P, Ritz D, Rueedi G..  (2020)  Optimization of LpxC Inhibitor Lead Compounds Focusing on Efficacy and Formulation for High Dose Intravenous Administration.,  63  (1): [PMID:31804829] [10.1021/acs.jmedchem.9b01605]

Source

Source(1):

• Scientific Literature