TPX-0005

TPX-0005 Structure
CAS No.
1802220-02-5
Chemical Name:
TPX-0005
Synonyms
Repotrectinib;TPX-005;Ropotrectinib;CS-2479;TPX-0005;Loprotinib;PX0005(Ropotrectinib);Ropotrectinib(TPX0005);TPX0005(Ropotrectinib);TPX-0005,Repotrectinib
CBNumber:
CB83312797
Molecular Formula:
C18H18FN5O2
Molecular Weight:
355.37
MOL File:
1802220-02-5.mol
Modify Date:
2024/7/2 8:55:27

TPX-0005 Properties

Density 1.46±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO:35.0(Max Conc. mg/mL);98.5(Max Conc. mM)
Ethanol:10.0(Max Conc. mg/mL);28.1(Max Conc. mM)
form A crystalline solid
pka 10.79±0.60(Predicted)
color White to off-white
InChI InChI=1S/C18H18FN5O2/c1-10-8-20-18(25)14-9-21-24-6-5-16(23-17(14)24)22-11(2)13-7-12(19)3-4-15(13)26-10/h3-7,9-11H,8H2,1-2H3,(H,20,25)(H,22,23)/t10-,11+/m0/s1
InChIKey FIKPXCOQUIZNHB-WDEREUQCSA-N
SMILES O1C2=CC=C(F)C=C2[C@@H](C)NC2C=CN3C(N=2)=C(C=N3)C(=O)NC[C@@H]1C

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
NFPA 704
0
2 0

TPX-0005 Chemical Properties,Uses,Production

Description

Ropotrectinib (TPX-0005; TP Therapeutics, San Diego, CA, USA) is a nextgeneration ROS1 inhibitor, a novel three-dimensional macrocyle with a much smaller size (MW <370) than current ROS1 inhibitors. It was specifically designed to overcome resistance mutations. Preclinical studies have shown activity against gatekeeper and solvent mutations, including G2032R, D2033N, L2026M, S1986F/Y, L1951R, and kinases involved in bypass signaling such as focal adhesion kinase, SRC proto-oncogene, and non-receptor tyrosine kinase [102, 103].

Description

Repotrectinib, also known as TPX-0005, is a multikinase (ROS1, ALK, and TRKA/B/C) inhibitor that is tested in an ongoing first-in-human phase 1/2 trail (NCT03093116).

General Description

Class: receptor tyrosine kinase; Treatment: NSCLC; Other name: TPX-0005

Biological Activity

Repotrectinib is a potent inhibitor targeting solvent-front mutations (SFMs) of ROS1, pan-TRK, and ALK. It effectively inhibits the kinase activity of wild-type ROS1, TRKA-C, and ALK, along with their SFMs, with IC50 values ranging from 0.071 to 4.46 nM. The compound shows high potency against ROS1 and TRKA-C, with approximately 15-fold selectivity over ALK.

Clinical Use

Repotrectinib has advantage with central nervous system (CNS) penetration, aimed to target both wide-type (WT) and solvent-front mutations (SFM) kinases and other resistance mutations including ROS1-G2032R and ROS1-D2033N, TRKA-G595R, TRKB-G639R, TRKC-G623R, and ALK-G1202R.

target

Primary targets: NTRK, ROS, ALT

TPX-0005 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 158)Suppliers
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Zhengzhou Anhuida Chemical Co., Ltd +8615903659408 China 297 58 Inquiry
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TPX-0005 TPX-0005;TPX 0005;TPX0005 CS-2479 Repotrectinib(TPX-005) Repotrectinib,TPX-0005 1,15-Etheno-1H-pyrazolo[4,3-f][1,4,8,10]benzoxatriazacyclotridecin-4(5H)-one,11-fluoro-6,7,13,14-tetrahydro-7,13-dimethyl-, (7S,13R)- TPX-0005,Repotrectinib TPX0005(Ropotrectinib) Ropotrectinib(TPX0005) Loprotinib Ropotrectinib Repotrectinib TPX-005 (7S,13R)-11-Fluoro-6,7,13,14-tetrahydro-7,13-dimethyl-1,15-etheno-1H-pyrazolo[4,3-f][1,4,8,10]benzoxatriazacyclotridecin-4(5H)-one PX0005(Ropotrectinib) 1802220-02-5 180222-02-5 API 1802220-02-5