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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H35N5O4.C4H6O6
Molecular Weight 655.6954
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAPROMORELIN TARTRATE

SMILES

O[C@H]([C@@H](O)C(O)=O)C(O)=O.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=MJGRJCMGMFLOET-MYPSAZMDSA-N
InChI=1S/C28H35N5O4.C4H6O6/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;5-1(3(7)8)2(6)4(9)10/h4-13,22H,14-19,29H2,1-3H3,(H,30,35);1-2,5-6H,(H,7,8)(H,9,10)/t22-,28-;1-,2-/m11/s1

HIDE SMILES / InChI

Molecular Formula C4H6O6
Molecular Weight 150.0868
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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

2016
Palliative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Discovery and biological characterization of capromorelin analogues with extended half-lives.
2002 Nov 18
Pyrazolinone-piperidine dipeptide growth hormone secretagogues (GHSs). Discovery of capromorelin.
2003 Feb 20
Gastric motor effects of peptide and non-peptide ghrelin agonists in mice in vivo and in vitro.
2005 Aug
Growth hormone (GH)-releasing hormone and GH secretagogues in normal aging: Fountain of Youth or Pool of Tantalus?
2008
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 16:18:25 GMT 2023
Edited
by admin
on Fri Dec 15 16:18:25 GMT 2023
Record UNII
4150VMF5EP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAPROMORELIN TARTRATE
USAN  
USAN  
Official Name English
CP-424391-18
Code 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 L-(+)-TARTRATE (1:1)
Systematic Name English
CP-424,391-18
Code English
CAPROMORELIN TARTRATE [MI]
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*))-, (R-(R*,R*))-2,3-DIHYDROXYBUTANEDIOATE (1:1)
Common Name English
CAPROMORELIN TARTRATE [USAN]
Common Name English
CAPIMORELIN TARTRATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C76358
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
Code System Code Type Description
SMS_ID
300000033570
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
PUBCHEM
9852610
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
RXCUI
1986788
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
CAS
193273-69-7
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
MERCK INDEX
m11965
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
USAN
KK-100
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID60941001
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
DAILYMED
4150VMF5EP
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
NCI_THESAURUS
C78756
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
FDA UNII
4150VMF5EP
Created by admin on Fri Dec 15 16:18:25 GMT 2023 , Edited by admin on Fri Dec 15 16:18:25 GMT 2023
PRIMARY
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ACTIVE MOIETY