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

Stem definitionDrug idCAS RN
antibiotics, 6-aminopenicillanic acid derivatives 2297 551-27-9

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • propicillin
  • phenoxypropylpenicillin
major descriptor (64-84); on-line search PENICILLIN, PHENOXYMETHYL/AA (64-84); Index Medicus search PROPICILLIN (64-84); RN given refers to parent cpd(2S-(2alpha,5alpha,6beta))-isomer
  • Molecular weight: 378.44
  • Formula: C18H22N2O5S
  • CLOGP: 2.78
  • LIPINSKI: 0
  • HAC: 7
  • HDO: 2
  • TPSA: 95.94
  • ALOGS: -3.24
  • ROTB: 6

Drug dosage:

DoseUnitRoute
0.90 g O

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 -0.449 Moderate 0.69
caco2-efflux Caco-2 efflux ratio (BA/AB) 3.882 Moderate 0.69
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 1.503 10^-6 cm/s Moderate 0.69
dh-clint Dog hepatocyte intrinsic clearance 3.882 uL/min/10^6 cells Moderate 0.69
dppb Dog plasma protein binding (% unbound) 35.680 % Moderate 0.69
fcs-ppb Fetal calf serum protein binding (% unbound) 28.150 % Moderate 0.69
herg hERG pIC50 4.446 pIC50 Moderate 0.69
hh-clint Human hepatocyte intrinsic clearance 1.770 uL/min/10^6 cells Moderate 0.69
hlm-clint Human liver microsomal intrinsic clearance 3.459 uL/min/mg protein Moderate 0.69
hppb Human plasma protein binding (% unbound) 29.610 % Moderate 0.69
kinase-safety-class ACVR2A,ACVR2B,AURKA,AXL,BRAF,BTK,CAMK2D,CDK5,CDK9,DDR1,DYRK1B,EGFR,EIF2AK3,ERBB2,GRK2,GSK3B,ITK,JAK2,JAK3,MAP2K6,MAP3K7,MAPK7,MAPKAPK2,NTRK2,PDK1,PDK2,PDK4,PIK3CB,PIK3CG,PIM2,PRKDC,STK33,SYK,TEK,TGFBR1,ZAP70 36
kinase-selectivity-class AXL,GRK2,MAP2K6 3
mdck-mdr1-bcrp-efflux MDCK-MDR1-BCRP efflux ratio 0.766 Moderate 0.66
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 1.660 Moderate 0.69
mh-clint Mouse hepatocyte intrinsic clearance 11.749 Moderate 0.69
mppb Mouse plasma protein binding (% unbound) 28.760 Moderate 0.69
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 4.295 Moderate 0.69
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 21.440 % Moderate 0.69
rat-kpuu-brain Rat brain Kpuu 0.007 % Moderate 0.66
rh-clint Rat hepatocyte intrinsic clearance 5.610 uL/min/10^6 cells Moderate 0.69
rh-fuinc Rat hepatocyte fraction unbound in incubation 78.010 % Moderate 0.69
rppb Rat plasma protein binding (% unbound) 23.900 % Moderate 0.69
solubility-dd Solubility at pH 7.4 in DMSO 924.698 uM Moderate 0.69

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 J01CE03 ANTIINFECTIVES FOR SYSTEMIC USE
ANTIBACTERIALS FOR SYSTEMIC USE
BETA-LACTAM ANTIBACTERIALS, PENICILLINS
Beta-lactamase sensitive penicillins
MeSH PA D000890 Anti-Infective Agents
MeSH PA D000900 Anti-Bacterial Agents
CHEBI has role CHEBI:33282 antibacterial agent

Related Drugs by ATC class:

J01CE Beta-lactamase sensitive penicillins 9 drugs

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 2.79 acidic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

None

External reference:

IDSource
D08438 KEGG_DRUG
C0072176 UMLSCUI
CHEBI:52429 CHEBI
CHEMBL2105612 ChEMBL_ID
DB13660 DRUGBANK_ID
C100135 MESH_SUPPLEMENTAL_RECORD_UI
92879 PUBCHEM_CID
1345 INN_ID
8X1R260V33 UNII
DB13337 DRUGBANK_ID
33277 RXNORM
004958 NDDF
006447 NDDF
14706000 SNOMEDCT_US
387084009 SNOMEDCT_US

Pharmaceutical products:

None