N-(2-(((1,4-trans)-4-(3-(3-(Trifluoromethoxy)phenyl)-ureido)cyclohexyl)oxy)-5-(trifluoromethyl)phenyl)acetamide

ID: ALA4068373

PubChem CID: 117954773

Max Phase: Preclinical

Molecular Formula: C23H23F6N3O4

Molecular Weight: 519.44

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(=O)Nc1cc(C(F)(F)F)ccc1O[C@H]1CC[C@H](NC(=O)Nc2cccc(OC(F)(F)F)c2)CC1

Standard InChI:  InChI=1S/C23H23F6N3O4/c1-13(33)30-19-11-14(22(24,25)26)5-10-20(19)35-17-8-6-15(7-9-17)31-21(34)32-16-3-2-4-18(12-16)36-23(27,28)29/h2-5,10-12,15,17H,6-9H2,1H3,(H,30,33)(H2,31,32,34)/t15-,17-

Standard InChI Key:  RUEVHRIRBURBEG-JCNLHEQBSA-N

Molfile:  

     RDKit          2D

 36 38  0  0  0  0  0  0  0  0999 V2000
    8.9093   -8.6630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9081   -9.4826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6162   -9.8915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3258   -9.4821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3230   -8.6594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6144   -8.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8311   -8.6837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8299   -9.5032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5380   -9.9122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2476   -9.5027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2448   -8.6801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5362   -8.2748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9510   -8.2688    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6602   -8.6747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3664   -8.2635    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6633   -9.4919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0756   -8.6694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0764   -9.4851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7815   -9.8910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4901   -9.4832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4890   -8.6650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7793   -8.2547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1978   -9.8918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0292   -8.2482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7384   -8.6541    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   11.0261   -7.4310    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   11.7337   -7.8335    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    2.5378  -10.7293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8300  -11.1378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8298  -11.9550    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224  -10.7290    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    1.1185  -11.5397    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    9.6160  -10.7087    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.9082  -11.1171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9080  -11.9343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2006  -10.7084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  1  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12  7  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 17 15  1  6
 17 18  1  0
 17 22  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  1
 23  2  1  0
  5 24  1  0
 24 25  1  0
 24 26  1  0
 24 27  1  0
  9 28  1  0
 28 29  1  0
 29 30  1  0
 29 31  1  0
 29 32  1  0
  3 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  2  0
M  END

Associated Targets(non-human)

Eif2ak1 Eukaryotic translation initiation factor 2-alpha kinase 1 (86 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Biocomponents

Calculated Properties

Molecular Weight: 519.44Molecular Weight (Monoisotopic): 519.1593AlogP: 6.07#Rotatable Bonds: 6
Polar Surface Area: 88.69Molecular Species: NEUTRALHBA: 4HBD: 3
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.36CX Basic pKa: CX LogP: 5.39CX LogD: 5.39
Aromatic Rings: 2Heavy Atoms: 36QED Weighted: 0.40Np Likeness Score: -1.37

References

1. Yefidoff-Freedman R, Fan J, Yan L, Zhang Q, Dos Santos GRR, Rana S, Contreras JI, Sahoo R, Wan D, Young J, Dias Teixeira KL, Morisseau C, Halperin J, Hammock B, Natarajan A, Wang P, Chorev M, Aktas BH..  (2017)  Development of 1-((1,4-trans)-4-Aryloxycyclohexyl)-3-arylurea Activators of Heme-Regulated Inhibitor as Selective Activators of the Eukaryotic Initiation Factor 2 Alpha (eIF2α) Phosphorylation Arm of the Integrated Endoplasmic Reticulum Stress Response.,  60  (13): [PMID:28590739] [10.1021/acs.jmedchem.7b00059]

Source