1-(1-(2-Chloroacetyl)piperidin-4-yl)-3-(3,4-dichlorophenyl)urea

ID: ALA5282454

Chembl Id: CHEMBL5282454

Max Phase: Preclinical

Molecular Formula: C14H16Cl3N3O2

Molecular Weight: 364.66

Names and Identifiers

Canonical SMILES:  O=C(Nc1ccc(Cl)c(Cl)c1)NC1CCN(C(=O)CCl)CC1

Standard InChI:  InChI=1S/C14H16Cl3N3O2/c15-8-13(21)20-5-3-9(4-6-20)18-14(22)19-10-1-2-11(16)12(17)7-10/h1-2,7,9H,3-6,8H2,(H2,18,19,22)

Standard InChI Key:  ZZHZJMHOVXNWQO-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA5282454

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Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 364.66

Molecular Weight (Monoisotopic): 363.0308

AlogP: 3.34

#Rotatable Bonds: 3

Polar Surface Area: 61.44

Molecular Species: NEUTRAL

HBA: 2

HBD: 2

#RO5 Violations: 0

HBA (Lipinski): 5

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 13.27

CX Basic pKa:

CX LogP: 2.10

CX LogD: 2.10

Aromatic Rings: 1

Heavy Atoms: 22

QED Weighted: 0.81

Np Likeness Score: -2.03

References

1. Cheng R, Lv X, Bu H, Xu Q, Wu J, Xie K, Tang J, Wang L, Zhuang J, Zhang Y, Zhang Y, Yan C, Lai Y..  (2022)  Design, synthesis, and evaluation of 4(1H)-quinolinone and urea derivatives as KRAS^G12C inhibitors with potent antitumor activity against KRAS-mutant non-small cell lung cancer.,  244  [PMID:36228411] [10.1016/j.ejmech.2022.114808]

Source

Source(1):

• Scientific Literature