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

Stem definitionDrug idCAS RN
3355 93-60-7

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • methyl nicotinate
  • methyl 3-pyridinecarboxylate
erythema provoked is basis of a methylnicotinate test of anti-inflammatories
  • Molecular weight: 137.14
  • Formula: C7H7NO2
  • CLOGP: 0.77
  • LIPINSKI: 0
  • HAC: 3
  • HDO: 0
  • TPSA: 39.19
  • ALOGS: 0.15
  • ROTB: 2

Drug dosage:

None

ADMET properties:

PropertyValueReference
BA (Bioavailability) 68 %

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 0.885 High 1
caco2-efflux Caco-2 efflux ratio (BA/AB) 0.153 High 1
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 60.954 10^-6 cm/s High 1
dh-clint Dog hepatocyte intrinsic clearance 75.162 uL/min/10^6 cells High 1
dppb Dog plasma protein binding (% unbound) 74.210 % High 1
fcs-ppb Fetal calf serum protein binding (% unbound) 76.600 % High 1
herg hERG pIC50 3.749 pIC50 High 1
hh-clint Human hepatocyte intrinsic clearance 168.267 uL/min/10^6 cells High 1
hlm-clint Human liver microsomal intrinsic clearance 61.944 uL/min/mg protein High 1
hppb Human plasma protein binding (% unbound) 61.700 % High 1
kinase-safety-class ACVR2A,ACVR2B,ALK,AURKA,AXL,BRAF,BTK,CAMK2B,CAMK2D,CDK5,CDK9,CHEK1,DDR1,DYRK1B,EIF2AK3,EPHB4,ERBB2,FLT3,GRK2,GRK3,GSK3B,ITK,JAK1,JAK2,MAP3K21,MAP3K7,MAPK7,MAPK9,MARK4,MTOR,NTRK2,PAK4,PDK1,PDK2,PDPK1,PIK3CB,PIK3CD,PRKCD,PRKDC,SIK2,SIK3,STK33,SYK,TEK,TTK 45
kinase-selectivity-class AXL,BRAF,CDK9,DYRK1B,GRK2,PRKDC 6
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 0.650 High 1
mh-clint Mouse hepatocyte intrinsic clearance 276.694 High 1
mppb Mouse plasma protein binding (% unbound) 81.190 High 1
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 0.183 High 1
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 68.180 % High 1
rh-clint Rat hepatocyte intrinsic clearance 49.431 uL/min/10^6 cells High 1
rh-fuinc Rat hepatocyte fraction unbound in incubation 95.540 % High 1
rppb Rat plasma protein binding (% unbound) 70.050 % High 1
solubility-dd Solubility at pH 7.4 in DMSO 3.819 uM High 1

Approvals:

DateAgencyCompanyOrphan
None FDA

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
CHEBI has role CHEBI:25212 metabolite
CHEBI has role CHEBI:33231 antitubercular agent
CHEBI has role CHEBI:35469 antidepressant
CHEBI has role CHEBI:35474 anxiolytic drug
CHEBI has role CHEBI:35476 antipsychotic agent
CHEBI has role CHEBI:35480 analgesic
CHEBI has role CHEBI:35526 hypoglycemic agent
CHEBI has role CHEBI:35554 cardiovascular drug
CHEBI has role CHEBI:35610 antineoplastic agent
CHEBI has role CHEBI:35620 vasodilator agent
CHEBI has role CHEBI:35679 antilipemic drug
CHEBI has role CHEBI:35821 anticholesteremic drug
CHEBI has role CHEBI:50247 antidote
CHEBI has role CHEBI:64946 anti-HIV agent
CHEBI has role CHEBI:74518 anti-obesity agent
CHEBI has role CHEBI:75771 mouse metabolite
CHEBI has role CHEBI:75835 anti-anaemic agent
CHEBI has role CHEBI:76924 plant metabolite
CHEBI has role CHEBI:76971 <em>Escherichia coli</em> metabolite
CHEBI has role CHEBI:84087 human urinary metabolite
CHEBI has role CHEBI:84264 EC 3.5.1.19 (nicotinamidase) inhibitor
CHEBI has role CHEBI:145947 antiatherosclerotic agent
CHEBI has role CHEBI:231911 renoprotective agent

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

DiseaseRelationSNOMED_IDDOID
Joint pain indication 57676002




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 3.01 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
4020266 VUID
N0000179190 NUI
D04991 KEGG_DRUG
4017661 VANDF
4019440 VANDF
4020266 VANDF
C0066412 UMLSCUI
CHEBI:134761 CHEBI
NIO PDB_CHEM_ID
CHEMBL379845 ChEMBL_ID
7151 PUBCHEM_CID
DB13882 DRUGBANK_ID
C008473 MESH_SUPPLEMENTAL_RECORD_UI
7B1AVU9DJN UNII
29900 RXNORM
15230 MMSL
2275 MMSL
43641 MMSL
5169 MMSL
7161 MMSL
NOCODE MMSL
d00314 MMSL
001052 NDDF
001987 NDDF
273943001 SNOMEDCT_US
424803001 SNOMEDCT_US
425096006 SNOMEDCT_US
63639004 SNOMEDCT_US
C0027996 UMLSCUI
DB00627 DRUGBANK_ID
938 PUBCHEM_CID
CHEBI:15940 CHEBI
7B1AVU9DJN INXIGHT DRUGS

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
Arth Arrest HUMAN OTC DRUG LABEL 2 76018-100 CREAM 0.50 g TOPICAL OTC Monograph Drug 9 sections
Arth RX Topical Analgesic HUMAN OTC DRUG LABEL 2 76069-100 LOTION 0.50 g TOPICAL OTC Monograph Drug 11 sections
Nuvira HUMAN OTC DRUG LABEL 4 83295-3313 PATCH 0.00 g CUTANEOUS OTC Monograph Drug 14 sections