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

Stem definitionDrug idCAS RN
growth hormone release-stimulating peptides 5656 193273-66-4

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • capromorelin
  • CP-424391
  • capimorelin
  • capromorelin tartrate
A growth hormone secretagogue
  • Molecular weight: 505.62
  • Formula: C28H35N5O4
  • CLOGP: 2.70
  • LIPINSKI: 1
  • HAC: 9
  • HDO: 2
  • TPSA: 117.33
  • ALOGS: -4.40
  • ROTB: 9

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 1.262 High 1
caco2-efflux Caco-2 efflux ratio (BA/AB) 22.491 High 1
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 3.499 10^-6 cm/s High 1
dh-clint Dog hepatocyte intrinsic clearance 5.346 uL/min/10^6 cells High 1
dppb Dog plasma protein binding (% unbound) 46.550 % High 1
fcs-ppb Fetal calf serum protein binding (% unbound) 45.350 % High 1
herg hERG pIC50 4.562 pIC50 High 1
hh-clint Human hepatocyte intrinsic clearance 5.140 uL/min/10^6 cells High 1
hlm-clint Human liver microsomal intrinsic clearance 50.466 uL/min/mg protein High 1
hppb Human plasma protein binding (% unbound) 51.320 % High 1
mdck-mdr1-bcrp-efflux MDCK-MDR1-BCRP efflux ratio 11.324 High 1
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 7.709 High 1
mh-clint Mouse hepatocyte intrinsic clearance 28.445 High 1
mppb Mouse plasma protein binding (% unbound) 40.500 High 1
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 20.989 High 1
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 64.170 % High 1
rat-kpuu-brain Rat brain Kpuu 0.009 % High 1
rh-clint Rat hepatocyte intrinsic clearance 25.586 uL/min/10^6 cells High 1
rh-fuinc Rat hepatocyte fraction unbound in incubation 81.670 % High 1
rppb Rat plasma protein binding (% unbound) 40.390 % High 1
solubility-dd Solubility at pH 7.4 in DMSO 912.011 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:176497 geroprotector

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

None




🐶 Veterinary Drug Use

SpeciesUseRelation
Dogs Appetite stimulation Indication

🐶 Veterinary products

ProductApplicantIngredients
ENTYCE Elanco US Inc. 1
Elura Elanco US Inc. 1

Acid dissociation constants calculated using MoKa v3.0.0

None

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Growth hormone secretagogue receptor type 1 GPCR Ki 8.15 CHEMBL
Growth hormone secretagogue receptor type 1 GPCR EC50 8.52 CHEMBL

External reference:

IDSource
CHEBI:748461 CHEBI
CHEMBL113313 ChEMBL_ID
C433143 MESH_SUPPLEMENTAL_RECORD_UI
DB15205 DRUGBANK_ID
C1259613 UMLSCUI
CHEMBL6068501 ChEMBL_ID
7901 INN_ID
193273-69-7 SECONDARY_CAS_RN
D03373 KEGG_DRUG
216208 PUBCHEM_CID
018032 NDDF
018033 NDDF
0MQ44VUN84 UNII
1986787 RXNORM
0MQ44VUN84 INXIGHT DRUGS

Pharmaceutical products:

None