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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H35N5O4
Molecular Weight 505.6086
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAPROMORELIN

SMILES

CN1N=C2CCN(C[C@@]2(CC3=CC=CC=C3)C1=O)C(=O)[C@@H](COCC4=CC=CC=C4)NC(=O)C(C)(C)N

InChI

InChIKey=KVLLHLWBPNCVNR-SKCUWOTOSA-N
InChI=1S/C28H35N5O4/c1-27(2,29)25(35)30-22(18-37-17-21-12-8-5-9-13-21)24(34)33-15-14-23-28(19-33,26(36)32(3)31-23)16-20-10-6-4-7-11-20/h4-13,22H,14-19,29H2,1-3H3,(H,30,35)/t22-,28-/m1/s1

HIDE SMILES / InChI

Molecular Formula C28H35N5O4
Molecular Weight 505.6086
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including: https://www.ncbi.nlm.nih.gov/pubmed/19174493 | http://adisinsight.springer.com/drugs/800011628

Capromorelin is a potent ghrelin receptor agonist. Capromorelin is indicated for appetite stimulation in dogs. Plasma insulin-like growth factor-I (IGF-I) was elevated progressively over a 5-d course of daily oral dosing in dogs. In healthy older adults at risk for functional decline, administration of the capromorelin may improve body composition and physical function. Adverse events included fatigue, insomnia, and small increases in fasting glucose, glycosylated hemoglobin, and indices of insulin resistance.

Originator

Curator's Comment: # Pfizer Inc.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
7.0 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
ENTYCE

Approved Use

ENTYCE is indicated for appetite stimulation in dogs

Launch Date

1.46335675E12
Palliative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Effects of an oral growth hormone secretagogue in older adults.
2009 Apr
The prokinetic face of ghrelin.
2010
Evidence for functional ghrelin receptors on parasympathetic preganglionic neurons of micturition control pathways in the rat.
2010 Sep
Smaller cardiac cell size and reduced extra-cellular collagen might be beneficial for hearts of Ames dwarf mice.
2010 Sep 1
Patents

Sample Use Guides

Dog: 3 mg/kg body weight once daily
Route of Administration: Oral
In rat pituitary cell cultures, Capromorelin stimulated growth hormone release with an EC50 = 3 nM.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:42:17 UTC 2023
Edited
by admin
on Fri Dec 15 17:42:17 UTC 2023
Record UNII
0MQ44VUN84
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAPROMORELIN
INN  
INN  
Official Name English
CP-424,391
Code English
CAPIMORELIN
Common Name English
PROPANAMIDE, 2-AMINO-N-(2-(2,3,3A,4,6,7-HEXAHYDRO-2-METHYL-3-OXO-3A-(PHENYLMETHYL)-5H-PYRAZOLO(4,3-C)PYRIDIN-5-YL)-2-OXO-1-((PHENYLMETHOXY)METHYL)ETHYL)-2-METHYL-, (R-(R*,R*))-
Common Name English
CP-424391
Code English
capromorelin [INN]
Common Name English
2-AMINO-N-((1R)-1-(((3AR)-3A-BENZYL-2,3,3A,4,6,7-HEXAHYDRO-2-METHYL-3-OXO-5H-PYRAZOLO(4,3-C)PYRIDIN-5-YL)CARBONYL)-2-(BENZYLOXY)ETHYL)-2-METHYLPROPIONAMIDE
Common Name English
CAPROMORELIN [MI]
Common Name English
CAPROMORELIN [GREEN BOOK]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 520.292
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
NCI_THESAURUS C76358
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
Code System Code Type Description
CAS
329327-00-6
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
SUPERSEDED
MERCK INDEX
m11965
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
EPA CompTox
DTXSID5057886
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
DAILYMED
0MQ44VUN84
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
RXCUI
1986787
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
INN
7901
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
PUBCHEM
216208
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
CAS
193273-66-4
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
WIKIPEDIA
Capromorelin
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
FDA UNII
0MQ44VUN84
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
DRUG BANK
DB15205
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
NCI_THESAURUS
C78754
Created by admin on Fri Dec 15 17:42:17 UTC 2023 , Edited by admin on Fri Dec 15 17:42:17 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY