(2-(4-Amino-6-(phenethylamino)-1,3,5-triazin-2-yl)-3-fluorophenyl)methanol

ID: ALA4567802

PubChem CID: 155560723

Max Phase: Preclinical

Molecular Formula: C18H18FN5O

Molecular Weight: 339.37

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  Nc1nc(NCCc2ccccc2)nc(-c2c(F)cccc2CO)n1

Standard InChI:  InChI=1S/C18H18FN5O/c19-14-8-4-7-13(11-25)15(14)16-22-17(20)24-18(23-16)21-10-9-12-5-2-1-3-6-12/h1-8,25H,9-11H2,(H3,20,21,22,23,24)

Standard InChI Key:  DJXHTVIPEBWGAJ-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

 25 27  0  0  0  0  0  0  0  0999 V2000
   37.8742  -18.2423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8730  -19.0618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.5811  -19.4708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.2907  -19.0614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.2879  -18.2387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.5793  -17.8335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.9910  -17.8287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.7006  -18.2364    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   41.4062  -17.8258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.4036  -17.0077    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   40.6894  -16.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.9866  -17.0149    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   42.1153  -18.2321    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   42.8217  -17.8212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.6834  -15.7848    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   38.5768  -17.0163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8679  -16.6098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   43.5307  -18.2274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.2371  -17.8165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.9420  -18.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.6479  -17.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.6457  -16.9970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.9316  -16.5909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.2287  -17.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.9991  -19.4689    0.0000 F   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
  5  7  1  0
  9 13  1  0
 13 14  1  0
 11 15  1  0
  6 16  1  0
 16 17  1  0
 14 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 19  1  0
  4 25  1  0
M  END

Alternative Forms

  1. Parent:

    ALA4567802

    ---

Associated Targets(Human)

GPR68 Tchem Ovarian cancer G-protein coupled receptor 1 (279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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

Calculated Properties

Molecular Weight: 339.37Molecular Weight (Monoisotopic): 339.1495AlogP: 2.41#Rotatable Bonds: 6
Polar Surface Area: 96.95Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 5.57CX LogP: 3.57CX LogD: 3.56
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.64Np Likeness Score: -0.95

References

1. Yu X, Huang XP, Kenakin TP, Slocum ST, Chen X, Martini ML, Liu J, Jin J..  (2019)  Design, Synthesis, and Characterization of Ogerin-Based Positive Allosteric Modulators for G Protein-Coupled Receptor 68 (GPR68).,  62  (16): [PMID:31298539] [10.1021/acs.jmedchem.9b00869]

Source