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Details

Stereochemistry ABSOLUTE
Molecular Formula C33H43FN10O6
Molecular Weight 694.7563
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NEMIFITIDE

SMILES

[H][C@]1(C[C@@H](O)CN1C(=O)[C@@H](N)CC2=CC=C(F)C=C2)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](CC3=CNC4=C3C=CC=C4)C(N)=O

InChI

InChIKey=SGXPTOACEHQGHL-RCNLLYRESA-N
InChI=1S/C33H43FN10O6/c34-20-9-7-18(8-10-20)12-23(35)32(50)44-17-21(45)14-27(44)31(49)43-25(6-3-11-39-33(37)38)30(48)41-16-28(46)42-26(29(36)47)13-19-15-40-24-5-2-1-4-22(19)24/h1-2,4-5,7-10,15,21,23,25-27,40,45H,3,6,11-14,16-17,35H2,(H2,36,47)(H,41,48)(H,42,46)(H,43,49)(H4,37,38,39)/t21-,23+,25+,26+,27+/m1/s1

HIDE SMILES / InChI

Molecular Formula C33H43FN10O6
Molecular Weight 694.7563
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Nemifitide is a peptide analog of melanocyte-inhibiting factor (MIF) that has been reported to relieve depressive symptoms in a very short period. Tetragenex (formerly Innapharma) was developing nemifitide with potential in the treatment of depression. Clinical data obtained from two pilot clinical studies, double-blind, placebo-controlled, parallel-design, in-patient and outpatient, suggested that nemifitide may have the following advantages over current therapies: rapid onset of action (3–5 d), short period of administration (5–10 doses over a 1–2 wk period), and a relatively long duration of treatment effect (3–6 months). The mechanism of action of nemifitide was investigated by evaluating its in-vitro receptor binding and in-vivo localization in the rat brain as well as its interactions with psychoprobes indicative of specific neurotransmitter pathways in acute studies in rats. The results of these studies indicate that nemifitide readily crosses the blood–brain barrier and is localized mainly in the amygdala, hippocampus and frontal cortex of the rat brain. Its in-vitro binding to several receptors including 5-HT-2A, as well as its significant interaction with d-fenfluramine in the rat, suggest the participation of the serotonergic pathway in its mode of action in a different way than that observed with SSRI antidepressants.

Approval Year

PubMed

PubMed

TitleDatePubMed
Clinical pharmacokinetic studies with INN 00835 (nemifitide), a novel pentapeptide antidepressant.
2002 Jan

Sample Use Guides

Doses of 18, 36, 54 and 72 mg/d showed almost equal clinical effect of duration between retreatment doses, the 36 mg/d dose being the most reproducible. The range of dose from 18 to 72 mg/d looks promising for the future clinical trials. Nemifitide was administered subcutaneously.
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:15:21 GMT 2023
Edited
by admin
on Sat Dec 16 16:15:21 GMT 2023
Record UNII
RO19OXA9NG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEMIFITIDE
INN   MI  
INN  
Official Name English
NEMIFITIDE [MI]
Common Name English
4-FLUORO-L-PHENYLALANYL-(4R)-4-HYDROXY-L-PROLYL-L-ARGINYLGLYCYL-L-TRYPTOPHANAMIDE
Common Name English
L-TRYPTOPHANAMIDE, 4-FLUORO-L-PHENYLALANYL-(4R)-4-HYDROXY-L-PROLYL-L-ARGINYLGLYCYL-
Common Name English
nemifitide [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C265
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C90713
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107761
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID101336172
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
PRIMARY
CAS
173240-15-8
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
PRIMARY
INN
8214
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
PRIMARY
PUBCHEM
6918348
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
PRIMARY
FDA UNII
RO19OXA9NG
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
PRIMARY
WIKIPEDIA
Nemifitide
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
PRIMARY
MERCK INDEX
m7800
Created by admin on Sat Dec 16 16:15:22 GMT 2023 , Edited by admin on Sat Dec 16 16:15:22 GMT 2023
PRIMARY Merck Index
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SALT/SOLVATE -> PARENT
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ACTIVE MOIETY