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Details

Stereochemistry ABSOLUTE
Molecular Formula C38H49N9O5
Molecular Weight 711.853
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IPAMORELIN

SMILES

CC(C)(N)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@H](CC2=CC3=CC=CC=C3C=C2)C(=O)N[C@H](CC4=CC=CC=C4)C(=O)N[C@@H](CCCCN)C(N)=O

InChI

InChIKey=NEHWBYHLYZGBNO-BVEPWEIPSA-N
InChI=1S/C38H49N9O5/c1-38(2,41)37(52)47-32(21-28-22-42-23-43-28)36(51)46-31(20-25-15-16-26-12-6-7-13-27(26)18-25)35(50)45-30(19-24-10-4-3-5-11-24)34(49)44-29(33(40)48)14-8-9-17-39/h3-7,10-13,15-16,18,22-23,29-32H,8-9,14,17,19-21,39,41H2,1-2H3,(H2,40,48)(H,42,43)(H,44,49)(H,45,50)(H,46,51)(H,47,52)/t29-,30+,31+,32-/m0/s1

HIDE SMILES / InChI
Ipamorelin is a new and potent synthetic pentapeptide which has distinct and specific growth hormone (GH)-releasing properties. Ipamorelin mimics ghrelin and binds to the ghrelin receptor (or GH secretagogue receptor, GHSR) in the brain, thereby selectively stimulating the release of GH from the pituitary gland. This results in increased plasma GH levels, which would affect many biological processes. Besides its presence in the brain, GHSR can also be found in the gastrointestinal tract, heart, lung, liver, kidney, pancreas, adipose tissue and immune cells. Unlike other GH releasing peptides, ipamorelin only stimulates GH release in a manner very similar to that of growth hormone releasing hormone.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacokinetic-pharmacodynamic modeling of ipamorelin, a growth hormone releasing peptide, in human volunteers.
1999 Sep
Patents

Patents

Sample Use Guides

Ipamorelin 0.06 mg/kg, TID (3 investigational drug infusions)
Route of Administration: Intravenous
Name Type Language
IPAMORELIN
INN  
INN  
Official Name English
NNC 26-0161
Code English
2-METHYLALANYL-L-HISTIDYL-3-(2-NAPHTHYL)-D-ALANYL-D-PHENYLALANYL-L-LYSINAMIDE
Common Name English
ipamorelin [INN]
Common Name English
NNC-260161
Code English
Ipamorelin [WHO-DD]
Common Name English
AIB-HIS-D-2-NAL-D-PHE-LYS-NH2
Common Name English
NNC-26-0161
Code English
Classification Tree Code System Code
NCI_THESAURUS C76358
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
WIKIPEDIA Designer-drugs-Ipamorelin
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID80168955
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
PRIMARY
EVMPD
SUB08269MIG
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
PRIMARY
SMS_ID
100000083138
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
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WIKIPEDIA
IPAMORELIN
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
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FDA UNII
Y9M3S784Z6
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
PRIMARY
INN
7639
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
PRIMARY
NCI_THESAURUS
C81120
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
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DRUG BANK
DB12370
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
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MESH
C114611
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
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ChEMBL
CHEMBL58547
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
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CAS
170851-70-4
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
PRIMARY
PUBCHEM
9831659
Created by admin on Fri Dec 15 16:37:16 GMT 2023 , Edited by admin on Fri Dec 15 16:37:16 GMT 2023
PRIMARY