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| SKU | Size | Availability |
Price | Qty |
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T421775-1ml
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1ml |
Available within 8-12 weeks(?)
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$241.90
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TrkA Selective Inhibitors
| 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 |
| Shipped In |
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. |
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 |
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| ALogP | 2.17 |
|---|---|
| HBD Count | 2 |
| Rotatable Bond | 12 |
| 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 |
| 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 |
| 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). |