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Taletrectinib (DS-6051b) - 10mM in DMSO, high purity , CAS No.1505515-69-4

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
T421775
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T421775-1ml
1ml
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$241.90

TrkA Selective Inhibitors

Basic Description

Synonyms Taletrectinib | DS-6051b | 1505515-69-4 | Taletrectinib adipate | DS-6051B adipate | 6KLL51GNBG | Taletrectinib adipate [USAN] | 1505515-69-4 (adipate) | 3-(4-((R)-2-Aminopropoxy)phenyl)-N-((R)-1-(3-fluorophenyl)ethyl)imidazo[1,2-b]pyridazin-6-amine adipate | 3-[4-[(2R)-2-
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms Taletrectinib (DS-6051b, AB-106) is a new-generation selective ROS1/NTRK inhibitor with ic50 of 0.207 nM,0.622 nM,2.28 nM and 0.980 nM for ROS1,NTRK1,NTRK2 and NTRK3,respectively.
Storage Temp Store at -80°C
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Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Information

Taletrectinib (DS-6051b, AB-106) is a new-generation selectiveROS1/NTRKinhibitor with ic50 of 0.207 nM,0.622 nM,2.28 nM and 0.980 nM for ROS1,NTRK1,NTRK2 and NTRK3,respectively.

Targets

ROS1 (Cell-free assay); TrkA (Cell-free assay); TrkC (Cell-free assay); TrkB (Cell-free assay) 0.207 nM; 0.622 nM; 0.980 nM; 2.28 nM

In vitro

DS-6051b inhibited the growth of the CD74-ROS1 overexpressed Ba/F3 cells and the ROS1 fusion-positive HCC78 cancer cell line.DS-6051b potently inhibited autophosphorylation of ROS1 in CD74-ROS1–expressed Ba/F3 cells and the SLC34A2-ROS1 harboring HCC78 cells at approximately single-digit to double-digit nanomolar concentration.

In vivo

In vivo experiments using the KM12-bearing mouse xenograft model shows that DS-6051b induced tumor shrinkage at a ≥50\u2009mg/kg or higher treatment dose without significant body weight loss.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Azoles
Subclass Imidazoles
Intermediate Tree Nodes Substituted imidazoles
Direct Parent Phenylimidazoles
Alternative Parents Phenoxy compounds  Phenol ethers  Medium-chain fatty acids  Alkyl aryl ethers  Aminopyridazines  Fluorobenzenes  N-substituted imidazoles  Aryl fluorides  Imidolactams  Dicarboxylic acids and derivatives  Heteroaromatic compounds  Azacyclic compounds  Carboxylic acids  Carbonyl compounds  Hydrocarbon derivatives  Monoalkylamines  Organic oxides  Organofluorides  
Molecular Framework Not available
Substituents 5-phenylimidazole - 4-phenylimidazole - Phenoxy compound - Phenol ether - Medium-chain fatty acid - Alkyl aryl ether - Aminopyridazine - Halobenzene - Fluorobenzene - N-substituted imidazole - Imidolactam - Benzenoid - Fatty acid - Pyridazine - Dicarboxylic acid or derivatives - Fatty acyl - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Heteroaromatic compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Ether - Organooxygen compound - Primary amine - Organic oxygen compound - Amine - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Primary aliphatic amine - Organofluoride - Organohalogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as phenylimidazoles. These are polycyclic aromatic compounds containing a benzene ring linked to an imidazole ring through a CC or CN bond.
External Descriptors Not available

Product Properties

ALogP 2.17
HBD Count 2
Rotatable Bond 12

Names and Identifiers

IUPAC Name 3-[4-[(2R)-2-aminopropoxy]phenyl]-N-[(1R)-1-(3-fluorophenyl)ethyl]imidazo[1,2-b]pyridazin-6-amine;hexanedioic acid
INCHI InChI=1S/C23H24FN5O.C6H10O4/c1-15(25)14-30-20-8-6-17(7-9-20)21-13-26-23-11-10-22(28-29(21)23)27-16(2)18-4-3-5-19(24)12-18;7-5(8)3-1-2-4-6(9)10/h3-13,15-16H,14,25H2,1-2H3,(H,27,28);1-4H2,(H,7,8)(H,9,10)/t15-,16-;/m1./s1
InChIKey DORJQZDOULKINH-QNBGGDODSA-N
Smiles CC(COC1=CC=C(C=C1)C2=CN=C3N2N=C(C=C3)NC(C)C4=CC(=CC=C4)F)N.C(CCC(=O)O)CC(=O)O
Isomeric SMILES C[C@H](COC1=CC=C(C=C1)C2=CN=C3N2N=C(C=C3)N[C@H](C)C4=CC(=CC=C4)F)N.C(CCC(=O)O)CC(=O)O
PubChem CID 72694302
Molecular Weight 551.61

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

DMSO(mg / mL) Max Solubility 50
DMSO(mM) Max Solubility 90.6437519261797
Water(mg / mL) Max Solubility <1
Molecular Weight 551.600 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 10
Rotatable Bond Count 12
Exact Mass 551.254 Da
Monoisotopic Mass 551.254 Da
Topological Polar Surface Area 152.000 Ų
Heavy Atom Count 40
Formal Charge 0
Complexity 645.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 2
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Citations of This Product

1. Jiawen Yang, Yifan Wu, Qiaoliang Zhu, Xiaojuan Qu, Hongyue Ou, Haixia Liu, Yongqi Wei, Di Ge, Chunlai Lu, Biao Jiang, Xiaoling Song.  (2024)  Discovery of a first-in-class protein degrader for the c-ros oncogene 1 (ROS1).  BIOORGANIC CHEMISTRY,  150  (107590). 

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