N-[4-(1H-Pyrrol-2-yl)-thiazol-2-yl]-guanidine: (maleate)

ID: ALA1744211

Max Phase: Preclinical

Molecular Formula: C12H13N5O4S

Molecular Weight: 207.26

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  N=C(N)Nc1nc(-c2ccc[nH]2)cs1.O=C(O)/C=C\C(=O)O

Standard InChI:  InChI=1S/C8H9N5S.C4H4O4/c9-7(10)13-8-12-6(4-14-8)5-2-1-3-11-5;5-3(6)1-2-4(7)8/h1-4,11H,(H4,9,10,12,13);1-2H,(H,5,6)(H,7,8)/b;2-1-

Standard InChI Key:  HADPSUQMPQOFPS-BTJKTKAUSA-N

Molfile:  

     RDKit          2D

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    6.1668  -22.7394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6390  -22.0658    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4163  -22.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3377  -22.7567    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6563  -23.3958    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.0841  -21.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5086  -22.7567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4336  -23.1309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3490  -21.0294    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.7463  -22.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1782  -21.0467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4200  -21.8354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0940  -22.0312    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0826  -23.4649    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8045  -18.0543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6295  -18.0543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3920  -18.7687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0420  -18.7687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8670  -18.7687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6295  -19.4832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5670  -18.7687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8045  -19.4832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0
  3  2  1  0
  4  1  1  0
  5  1  1  0
  6  3  1  0
  7  4  1  0
  8  5  1  0
  9  6  1  0
 10  6  2  0
 11  9  1  0
 12 10  1  0
 13  7  2  0
 14  7  1  0
  3  8  2  0
 11 12  2  0
 15 16  2  0
 15 17  1  0
 16 18  1  0
 18 19  2  0
 18 20  1  0
 17 21  1  0
 17 22  2  0
M  END

Associated Targets(Human)

ATP4A Tclin Potassium-transporting ATPase (493 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

Calculated Properties

Molecular Weight: 207.26Molecular Weight (Monoisotopic): 207.0579AlogP: 1.44#Rotatable Bonds: 2
Polar Surface Area: 90.58Molecular Species: NEUTRALHBA: 3HBD: 4
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 5#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 7.71CX LogP: 1.32CX LogD: 0.85
Aromatic Rings: 2Heavy Atoms: 14QED Weighted: 0.44Np Likeness Score: -1.67

References

1. LaMattina JL, McCarthy PA, Reiter LA, Holt WF, Yeh LA..  (1990)  Antiulcer agents. 4-substituted 2-guanidinothiazoles: reversible, competitive, and selective inhibitors of gastric H+,K(+)-ATPase.,  33  (2): [PMID:2153817] [10.1021/jm00164a012]

Source