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Details

Stereochemistry ABSOLUTE
Molecular Formula C46H73N13O11S2
Molecular Weight 1048.282
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SELEPRESSIN

SMILES

CC[C@H](C)[C@@H]1NC(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCC(N)=O)NC1=O)C(=O)N3CCC[C@H]3C(=O)N[C@@H](CCCNC(C)C)C(=O)NCC(N)=O

InChI

InChIKey=JCVQBJTWWDYUFQ-MRUTUVJXSA-N
InChI=1S/C46H73N13O11S2/c1-5-26(4)38-45(69)54-30(14-9-17-35(48)60)41(65)56-32(21-36(49)61)42(66)57-33(24-72-71-23-28(47)39(63)55-31(43(67)58-38)20-27-12-7-6-8-13-27)46(70)59-19-11-16-34(59)44(68)53-29(15-10-18-51-25(2)3)40(64)52-22-37(50)62/h6-8,12-13,25-26,28-34,38,51H,5,9-11,14-24,47H2,1-4H3,(H2,48,60)(H2,49,61)(H2,50,62)(H,52,64)(H,53,68)(H,54,69)(H,55,63)(H,56,65)(H,57,66)(H,58,67)/t26-,28-,29-,30-,31-,32-,33-,34-,38-/m0/s1

HIDE SMILES / InChI

Molecular Formula C46H73N13O11S2
Molecular Weight 1048.282
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Selepressin (FE 202158) was designed as a selective and short-acting vasopressin type 1a receptor (V(1a)R) agonist. This drug was developed for the treatment of vasodilatory hypotension in shock. Selepressin successfully completed phase IIa clinical trial, where was found that in septic shock patients, selepressin 2.5 ng/kg/minute was able to rapidly replace norepinephrine, improve fluid balance and shorten the time of mechanical ventilation.

Approval Year

PubMed

PubMed

TitleDatePubMed
Selepressin and Arginine Vasopressin Do Not Display Cardiovascular Risk in Atherosclerotic Rabbit.
2016

Sample Use Guides

This was a randomized, double-blind, placebo-controlled multicenter trial in 53 patients in early septic shock (aged ≥18 years, fluid resuscitation, requiring vasopressor support) who received selepressin 1.25 ng/kg/minute (n = 10), 2.5 ng/kg/minute (n = 19), 3.75 ng/kg/minute (n = 2), or placebo (n = 21) until shock resolution or a maximum of 7 days
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:50:13 UTC 2023
Edited
by admin
on Sat Dec 16 01:50:13 UTC 2023
Record UNII
8P2T76M0SJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SELEPRESSIN
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
SELEPRESSIN [USAN]
Common Name English
(2-L-PHENYLALANINE,3-L-ISOLEUCINE,4-(6-OXO-L-LYSINE), 8-(5-N-(PROPAN-2-YL)-L-ORNITHINE))HUMAN VASOPRESSIN
Systematic Name English
GLYCINAMIDE, L-CYSTEINYL-L-PHENYLALANYL-L-ISOLEUCYL-6-OXO-L-LYSYL-L-ASPARAGINYL-L-CYSTEINYL-L-PROLYL-N5-(1-METHYLETHYL)-L-ORNITHYL-, CYCLIC (1-6)-DISULFIDE
Common Name English
FE202158
Code English
Selepressin [WHO-DD]
Common Name English
selepressin [INN]
Common Name English
FE-202158
Code English
Classification Tree Code System Code
NCI_THESAURUS C80212
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
Code System Code Type Description
USAN
BC-116
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
WIKIPEDIA
Selepressin
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
ChEMBL
CHEMBL1817709
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
INN
9418
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
PUBCHEM
53330936
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
FDA UNII
8P2T76M0SJ
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
NCI_THESAURUS
C152319
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
EPA CompTox
DTXSID90236538
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
DRUG BANK
DB12495
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
CAS
876296-47-8
Created by admin on Sat Dec 16 01:50:13 UTC 2023 , Edited by admin on Sat Dec 16 01:50:13 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
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ACTIVE MOIETY