(2-(4-Amino-6-((3-methoxybenzyl)amino)-1,3,5-triazin-2-yl)phenyl)methanol

ID: ALA4555012

PubChem CID: 155556643

Max Phase: Preclinical

Molecular Formula: C18H19N5O2

Molecular Weight: 337.38

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cccc(CNc2nc(N)nc(-c3ccccc3CO)n2)c1

Standard InChI:  InChI=1S/C18H19N5O2/c1-25-14-7-4-5-12(9-14)10-20-18-22-16(21-17(19)23-18)15-8-3-2-6-13(15)11-24/h2-9,24H,10-11H2,1H3,(H3,19,20,21,22,23)

Standard InChI Key:  MXGCUBBSDAFSAP-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

 25 27  0  0  0  0  0  0  0  0999 V2000
   38.0186  -12.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.0175  -13.0485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.7255  -13.4574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.4352  -13.0480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.4323  -12.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.7237  -11.8201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.1355  -11.8154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.8450  -12.2230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   41.5507  -11.8124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.5481  -10.9944    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   40.8338  -10.5886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.1311  -11.0015    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   42.2597  -12.2187    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   42.9661  -11.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.6752  -12.2141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.6743  -13.0307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.3825  -13.4369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.0898  -13.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.0845  -12.2045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.3757  -11.8021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.8279   -9.7715    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   38.7213  -11.0029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.0124  -10.5964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   44.3848  -14.2541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   43.6782  -14.6647    0.0000 C   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
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 15  1  0
 11 21  1  0
  6 22  1  0
 22 23  1  0
 17 24  1  0
 24 25  1  0
M  END

Alternative Forms

  1. Parent:

    ALA4555012

    ---

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: 337.38Molecular Weight (Monoisotopic): 337.1539AlogP: 2.23#Rotatable Bonds: 6
Polar Surface Area: 106.18Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 6.45CX LogP: 2.95CX LogD: 2.91
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.63Np Likeness Score: -0.88

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