ID: ALA4226506

Max Phase: Preclinical

Molecular Formula: C27H36BrN3O6S

Molecular Weight: 610.57

Molecule Type: Small molecule

Representations

Canonical SMILES:  Cc1noc(C)c1S(=O)(=O)NCCO/N=C1\C[C@H]2[C@](C)(C(=O)O)CCC[C@]2(C)c2cc(Br)c(C(C)C)cc21

Standard InChI:  InChI=1S/C27H36BrN3O6S/c1-15(2)18-12-19-20(13-21(18)28)26(5)8-7-9-27(6,25(32)33)23(26)14-22(19)31-36-11-10-29-38(34,35)24-16(3)30-37-17(24)4/h12-13,15,23,29H,7-11,14H2,1-6H3,(H,32,33)/b31-22+/t23-,26-,27-/m1/s1

Standard InChI Key:  SNOHQZGATSEJIT-OBDQHKETSA-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: 610.57

Molecular Weight (Monoisotopic): 609.1508

AlogP: 5.43

#Rotatable Bonds: 8

Polar Surface Area: 131.09

Molecular Species: ACID

HBA: 7

HBD: 2

#RO5 Violations: 2

HBA (Lipinski): 9

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 3.63

CX Basic pKa: 2.41

CX LogP: 4.88

CX LogD: 1.70

Aromatic Rings: 2

Heavy Atoms: 38

QED Weighted: 0.30

Np Likeness Score: 0.12

References

1. Zhang WM, Yao Y, Yang T, Wang XY, Zhu ZY, Xu WT, Lin HX, Gao ZB, Zhou H, Yang CG, Cui YM..  (2018)  The synthesis and antistaphylococcal activity of N-sulfonaminoethyloxime derivatives of dehydroabietic acid.,  28  (10): [PMID:29650291] [10.1016/j.bmcl.2018.03.062]

Source

Source(1):

• Scientific Literature