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Details

Stereochemistry ABSOLUTE
Molecular Formula C51H84N16O21
Molecular Weight 1257.3073
Optical Activity UNSPECIFIED
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CIBINETIDE

SMILES

CC(C)C[C@H](NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H]1CCC(=O)N1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O

InChI

InChIKey=WZTIQQBMSJTRBR-WYKNNRPVSA-N
InChI=1S/C51H84N16O21/c1-22(2)17-30(47(84)65-32(19-36(53)71)48(85)66-33(20-68)49(86)67-34(21-69)50(87)88)63-40(77)24(5)57-41(78)25(7-6-16-56-51(54)55)59-43(80)29(11-15-39(75)76)62-46(83)31(18-23(3)4)64-45(82)27(8-12-35(52)70)60-44(81)28(10-14-38(73)74)61-42(79)26-9-13-37(72)58-26/h22-34,68-69H,6-21H2,1-5H3,(H2,52,70)(H2,53,71)(H,57,78)(H,58,72)(H,59,80)(H,60,81)(H,61,79)(H,62,83)(H,63,77)(H,64,82)(H,65,84)(H,66,85)(H,67,86)(H,73,74)(H,75,76)(H,87,88)(H4,54,55,56)/t24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-/m0/s1

HIDE SMILES / InChI

Molecular Formula C51H84N16O21
Molecular Weight 1257.3073
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 11 / 11
E/Z Centers 4
Optical Activity UNSPECIFIED

Cibinetide (ARA 290; helix B surface peptide) is a novel potent and selective peptide agonist of innate repair receptor (IRR) with anti-inflammatory and tissue-protective activities. IRR activation promotes tissue protection and repair in a wide variety of preclinical models, including diabetic wound healing, diabetic neuropathy, and ischemic retinopathy. In a mouse model of diabetic small nerve fiber loss, daily administration of Cibinetide reversed neuronal dystrophy. Cibinetide administration significantly improved re-epithelization, angiogenesis, and wound healing strength in a mouse model of diabetic wounds. In clinical studies, Cibinetide administration has shown significantly increased small nerve fiber abundance, reduced neuropathic symptoms and promoted nerve fiber repair in patients with sarcoidosis or diabetes-related nerve fiber loss.

Approval Year

PubMed

PubMed

TitleDatePubMed
The vasoreparative potential of endothelial colony-forming cells in the ischemic retina is enhanced by cibinetide, a non-hematopoietic erythropoietin mimetic.
2019 May
Patents

Patents

Sample Use Guides

1, 4, or 8 mg cibinetide or placebo daily for 28 days
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:25:22 GMT 2023
Edited
by admin
on Sat Dec 16 01:25:22 GMT 2023
Record UNII
9W5677JKDA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CIBINETIDE
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
L-SERINE, 5-OXO-L-PROLYL-L-.ALPHA.-GLUTAMYL-L-GLUTAMINYL-L-LEUCYL-L-.ALPHA.-GLUTAMYL-L-ARGINYL-L-ALANYL-L-LEUCYL-L-ASPARAGINYL-L-SERYL-
Systematic Name English
PYR-GLU-GLN-LEU-GLU-ARG-ALA-LEU-ASN-SER-SER-OH
Common Name English
ARA-290
Code English
PH-BSP
Common Name English
PHBSP
Common Name English
L-PYR-L-GLU-L-GLN-L-LEU-L-GLU-L-ARG-L-ALA-L-LEU-L-ASN-L-SER-L-SER
Common Name English
ARA290
Code English
Cibinetide [WHO-DD]
Common Name English
ARA 290
Code English
L-PYROGLUTAMYL-L-GLUTAMYL-L-GLUTAMINYL-L-IEUCYL-L-GLUTAMYL-L-ARGINYL-L-ALANYL-L-LEUCYL-L-ASPARAGINYL-L-SERYL-L-SERINE
Systematic Name English
CIBINETIDE [USAN]
Common Name English
L-PYROGLUTAMYL-L-GLUTAMYL-L-GLUTAMINYL-L-LEUCYL-L-GLUTAMYL-L-ARGINYL-L-ALANYL-L-LEUCYL-L-ASPARAGINYL-L-SERYL-L-SERINE
Systematic Name English
cibinetide [INN]
Common Name English
PGLU-GLU-GLN-LEU-GLU-ARG-ALA-LEU-ASN-SER-SER
Common Name English
Classification Tree Code System Code
EU-Orphan Drug EU/3/16/1721
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
FDA ORPHAN DRUG 523116
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
FDA ORPHAN DRUG 349111
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
FDA ORPHAN DRUG 523816
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
FDA ORPHAN DRUG 289609
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
Code System Code Type Description
PUBCHEM
91810664
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
PRIMARY
FDA UNII
9W5677JKDA
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
PRIMARY
USAN
BC-123
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
PRIMARY
CAS
1208243-50-8
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
PRIMARY
NCI_THESAURUS
C171683
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL3545305
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
PRIMARY
DRUG BANK
DB13006
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
PRIMARY
INN
10264
Created by admin on Sat Dec 16 01:25:22 GMT 2023 , Edited by admin on Sat Dec 16 01:25:22 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY