nicotinyl methylamide 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | PK/Tox | Related Drugs | BioActivity |

Stem definitionDrug idCAS RN
4862 114-33-0

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • nicotinyl methylamide
  • nicotinic acid methylamide
  • Molecular weight: 136.15
  • Formula: C7H8N2O
  • CLOGP: 0.11
  • LIPINSKI: 0
  • HAC: 3
  • HDO: 1
  • TPSA: 41.99
  • ALOGS: -0.87
  • ROTB: 1

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 0.221 High 1
caco2-efflux Caco-2 efflux ratio (BA/AB) 0.889 High 1
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 48.641 10^-6 cm/s High 1
dh-clint Dog hepatocyte intrinsic clearance 4.416 uL/min/10^6 cells High 1
dppb Dog plasma protein binding (% unbound) 78.330 % High 1
fcs-ppb Fetal calf serum protein binding (% unbound) 80.290 % High 1
herg hERG pIC50 3.516 pIC50 High 1
hh-clint Human hepatocyte intrinsic clearance 1.256 uL/min/10^6 cells High 1
hlm-clint Human liver microsomal intrinsic clearance 3.404 uL/min/mg protein High 1
hppb Human plasma protein binding (% unbound) 71.810 % High 1
kinase-safety-class ACVR2B,AXL,BRAF,CAMK2D,CDK5,CDK9,DDR1,DYRK1B,EIF2AK3,ERBB2,GRK2,GRK3,MAPK7,PDK1,PDK2,PDK4,PRKDC,SIK2,STK33,TEK 20
kinase-selectivity-class AXL,BRAF,CDK9,DYRK1B,GRK2,SIK2 6
mdck-mdr1-bcrp-efflux MDCK-MDR1-BCRP efflux ratio 0.741 High 1
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 1.954 High 1
mh-clint Mouse hepatocyte intrinsic clearance 6.592 High 1
mppb Mouse plasma protein binding (% unbound) 90.120 High 1
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 1.782 High 1
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 83.960 % High 1
rat-kpuu-brain Rat brain Kpuu 0.630 % High 1
rh-clint Rat hepatocyte intrinsic clearance 0.908 uL/min/10^6 cells High 1
rh-fuinc Rat hepatocyte fraction unbound in incubation 95.750 % High 1
rppb Rat plasma protein binding (% unbound) 68.730 % High 1
solubility-dd Solubility at pH 7.4 in DMSO 918.333 uM High 1

Approvals:

None

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC A05AB01 ALIMENTARY TRACT AND METABOLISM
BILE AND LIVER THERAPY
BILE THERAPY
Preparations for biliary tract therapy
CHEBI has role CHEBI:25212 metabolites

Drug Use | Suggest Off label Use Form| |View source of the data|

None




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 11.69 acidic
pKa2 3.05 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
CHEMBL11978 ChEMBL_ID
DB08840 DRUGBANK_ID
C0068144 UMLSCUI
CHEBI:64399 CHEBI
PJH PDB_CHEM_ID
64950 PUBCHEM_CID
X3I82S5L8I UNII

Pharmaceutical products:

None