(3S,2Z)-3-(2-Aminothiazol-4-yl)-2-[[(4-carbonylbenzyloxy)imino]acetamido]-4,4-dimethyl-2-oxoazetidinyl hydroxysulfonate

ID: ALA3764966

Chembl Id: CHEMBL3764966

PubChem CID: 127040378

Max Phase: Preclinical

Molecular Formula: C18H19N5O8S2

Molecular Weight: 497.51

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CC1(C)[C@H](NC(=O)/C(=N\OCc2ccc(C(=O)O)cc2)c2csc(N)n2)C(=O)N1S(=O)(=O)O

Standard InChI:  InChI=1S/C18H19N5O8S2/c1-18(2)13(15(25)23(18)33(28,29)30)21-14(24)12(11-8-32-17(19)20-11)22-31-7-9-3-5-10(6-4-9)16(26)27/h3-6,8,13H,7H2,1-2H3,(H2,19,20)(H,21,24)(H,26,27)(H,28,29,30)/b22-12-/t13-/m1/s1

Standard InChI Key:  JYIHMBITROCEQF-IKTNTUJMSA-N

Alternative Forms

1. Parent:

   

   ALA3764966

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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: 497.51

Molecular Weight (Monoisotopic): 497.0675

AlogP: 0.25

#Rotatable Bonds: 8

Polar Surface Area: 201.58

Molecular Species: ACID

HBA: 10

HBD: 4

#RO5 Violations: 0

HBA (Lipinski): 13

HBD (Lipinski): 5

#RO5 Violations (Lipinski): 1

CX Acidic pKa: -1.42

CX Basic pKa: 3.21

CX LogP: -1.89

CX LogD: -4.69

Aromatic Rings: 2

Heavy Atoms: 33

QED Weighted: 0.17

Np Likeness Score: -0.38

References

1. Fu HG, Hu XX, Li CR, Li YH, Wang YX, Jiang JD, Bi CW, Tang S, You XF, Song DQ..  (2016)  Design, synthesis and biological evaluation of monobactams as antibacterial agents against gram-negative bacteria.,  110  [PMID:26827160] [10.1016/j.ejmech.2016.01.024]

Source

Source(1):

• Scientific Literature