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Details

Stereochemistry ABSOLUTE
Molecular Formula C97H144FN33O19S2
Molecular Weight 2159.519
Optical Activity UNSPECIFIED
Defined Stereocenters 14 / 14
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MOTIXAFORTIDE

SMILES

[H][C@@]12CCCN1C(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@]([H])(CCCNC(N)=O)NC(=O)[C@H](CC3=CC=C(O)C=C3)NC(=O)[C@H](CSSC[C@]([H])(NC(=O)[C@H](CCCNC(N)=O)NC(=O)[C@]([H])(CCCNC(N)=N)NC(=O)[C@H](CC4=CC=C(O)C=C4)NC2=O)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O)NC(=O)[C@H](CC5=CC6=C(C=CC=C6)C=C5)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)C7=CC=C(F)C=C7

InChI

InChIKey=JJVZSYKFCOBILL-MKMRYRNGSA-N
InChI=1S/C97H144FN33O19S2/c98-60-33-31-58(32-34-60)78(135)119-65(19-8-42-113-93(104)105)79(136)121-68(21-10-44-115-95(108)109)83(140)126-73(51-56-25-30-57-14-1-2-15-59(57)48-56)87(144)130-75-53-152-151-52-74(88(145)118-63(77(101)134)18-7-41-112-92(102)103)129-84(141)69(23-12-46-117-97(111)150)122-81(138)66(20-9-43-114-94(106)107)124-86(143)72(50-55-28-37-62(133)38-29-55)128-90(147)76-24-13-47-131(76)91(148)70(17-4-6-40-100)125-82(139)64(16-3-5-39-99)120-80(137)67(22-11-45-116-96(110)149)123-85(142)71(127-89(75)146)49-54-26-35-61(132)36-27-54/h1-2,14-15,25-38,48,63-76,132-133H,3-13,16-24,39-47,49-53,99-100H2,(H2,101,134)(H,118,145)(H,119,135)(H,120,137)(H,121,136)(H,122,138)(H,123,142)(H,124,143)(H,125,139)(H,126,140)(H,127,146)(H,128,147)(H,129,141)(H,130,144)(H4,102,103,112)(H4,104,105,113)(H4,106,107,114)(H4,108,109,115)(H3,110,116,149)(H3,111,117,150)/t63-,64-,65-,66-,67-,68-,69-,70-,71-,72-,73-,74-,75-,76-/m0/s1

HIDE SMILES / InChI

Molecular Formula C97H144FN33O19S2
Molecular Weight 2159.519
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 14 / 14
E/Z Centers 7
Optical Activity UNSPECIFIED

BioLineRx Ltd has developed BL-8040, a short peptide for the treatment of solid tumors, acute myeloid leukemia, or AML, and stem-cell mobilization for bone-marrow transplantation. BL-8040 acts as CXCR4 antagonist. CXCR4 is a chemokine receptor that is directly involved in tumor progression, angiogenesis, metastasis, and cell survival. In February 2019 US Food and Drug Administration (FDA) has granted Orphan Drug Designation to BL-8040, for the treatment of pancreatic cancer. Previously FDA had granted Orphan Drug Designation for the treatment of acute myeloid leukemia and stem-cell mobilization.

Approval Year

PubMed

PubMed

TitleDatePubMed
T140 analogs as CXCR4 antagonists identified as anti-metastatic agents in the treatment of breast cancer.
2003 Aug 28
Single Dose of the CXCR4 Antagonist BL-8040 Induces Rapid Mobilization for the Collection of Human CD34(+) Cells in Healthy Volunteers.
2017 Nov 15

Sample Use Guides

Multiple Myeloma: BL-8040 1.25mg/kg + G-CSF. Up to 2 SC injections of BL-8040 are anticipated during the study
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Sat Dec 16 11:13:20 UTC 2023
Edited
by admin
on Sat Dec 16 11:13:20 UTC 2023
Record UNII
DA9G065962
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MOTIXAFORTIDE
USAN   INN  
Official Name English
BKT-140
Code English
S3.4,S3.13-CYCLO(N.ALPHA.-(4-FLUOROBENZOYL)-L-ARGINYL-L-ARGINYL-3-(NAPHTHALEN-2-YL)-L-ALANYL-L-CYSTEINYL-L-TYROSYL-N5-CARBAMOYL-L-ORNITHYL-L-LYSYL-D-LYSYL-L-PROLYL-L-TYROSYL-LARGINYL-N5-CARBAMOYL-L-ORNITHYL-L-CYSTEINYL-L-ARGININAMIDE)
Systematic Name English
T140
Code English
MOTIXAFORTIDE [USAN]
Common Name English
4F-BENZOYL-TN-14003
Code English
Motixafortide [WHO-DD]
Common Name English
BL-8040
Code English
N-(4-FLUORO-BENZOYL)-L-ARGINYL-L-ARGINYL-(L-3-(NAPHTHYL)ALANYL)-L-CYSTEINYL-L-TYROSYL-L-CITRULLINYL-L-LYSYL-D-LYSYL-L-PROLYL-L-TYROSYL-L-ARGINYL-L-CITRULLINYL-L-CYSTEINYL-L-ARGININE AMIDE,CYCLIC (4-13)-DISULFIDE
Common Name English
motixafortide [INN]
Common Name English
L-ARGININAMIDE, N2-(4-FLUOROBENZOYL)-L-ARGINYL-L-ARGINYL-3-(2-NAPHTHALENYL)-L-ALANYL-L-CYSTEINYL-L-TYROSYL-N5-(AMINOCARBONYL)-L-ORNITHYL-L-LYSYL-D-LYSYL-L-PROLYL-L-TYROSYL-L-ARGINYL-N5-(AMINOCARBONYL)-L-ORNITHYL-L-CYSTEINYL-, CYCLIC (4->13)-DISULFIDE
Systematic Name English
BKT140
Code English
TF-14016
Code English
Classification Tree Code System Code
FDA ORPHAN DRUG 669818
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
FDA ORPHAN DRUG 371912
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
FDA ORPHAN DRUG 403213
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
Code System Code Type Description
CAS
664334-36-5
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
PRIMARY
INN
10935
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
PRIMARY
PUBCHEM
91865076
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
PRIMARY
USAN
JK-257
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
PRIMARY
DRUG BANK
DB14939
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
PRIMARY
ChEMBL
CHEMBL3545348
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
PRIMARY
FDA UNII
DA9G065962
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
PRIMARY
CHEBI
145536
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
PRIMARY
NCI_THESAURUS
C88309
Created by admin on Sat Dec 16 11:13:20 UTC 2023 , Edited by admin on Sat Dec 16 11:13:20 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY