ID: ALA433378

Max Phase: Preclinical

Molecular Formula: C13H14N2Na2O8S2

Molecular Weight: 392.41

Molecule Type: Small molecule

Representations

Canonical SMILES:  CC(=O)N/C=C\SC1=C(C(=O)[O-])N2C(=O)[C@@H](C(C)OS(=O)(=O)[O-])[C@H]2C1.[Na+].[Na+]

Standard InChI:  InChI=1S/C13H16N2O8S2.2Na/c1-6(23-25(20,21)22)10-8-5-9(24-4-3-14-7(2)16)11(13(18)19)15(8)12(10)17;;/h3-4,6,8,10H,5H2,1-2H3,(H,14,16)(H,18,19)(H,20,21,22);;/q;2*+1/p-2/b4-3-;;/t6?,8-,10+;;/m1../s1

Standard InChI Key:  HESFZADEDUAEQE-RBRLJPCBSA-L

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: 392.41

Molecular Weight (Monoisotopic): 392.0348

AlogP: 0.06

#Rotatable Bonds: 7

Polar Surface Area: 150.31

Molecular Species: ACID

HBA: 7

HBD: 3

#RO5 Violations: 0

HBA (Lipinski): 10

HBD (Lipinski): 3

#RO5 Violations (Lipinski): 0

CX Acidic pKa: -1.85

CX Basic pKa:

CX LogP: -2.23

CX LogD: -8.04

Aromatic Rings: 0

Heavy Atoms: 25

QED Weighted: 0.40

Np Likeness Score: 0.83

References

1. Harada S, Tsubotani S, Asai M, Okonogi K, Kondo M..  (1983)  Synthesis and biological activities of the Z isomers of carbapenem antibiotics.,  26  (2): [PMID:6402596] [10.1021/jm00356a029]

2. Harada S, Tsubotani S, Asai M, Okonogi K, Kondo M..  (1983)  Synthesis and biological activities of the Z isomers of carbapenem antibiotics.,  26  (5): [PMID:6341590] [10.1021/jm00359a600]

Source

Source(1):

• Scientific Literature