2-Thiophenecarboxamide, N-[(1S)-1-cyclopropyl-2,2,2-trifluoroethyl]-4-[6-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]- manufacturers
- ULK-101
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- $107.00
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2026-07-17
- CAS:2443816-45-1
- Purity: 99.94%
- Supply Ability: 10g
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| | 2-Thiophenecarboxamide, N-[(1S)-1-cyclopropyl-2,2,2-trifluoroethyl]-4-[6-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]- Basic information |
| Product Name: | 2-Thiophenecarboxamide, N-[(1S)-1-cyclopropyl-2,2,2-trifluoroethyl]-4-[6-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]- | | Synonyms: | 2-Thiophenecarboxamide, N-[(1S)-1-cyclopropyl-2,2,2-trifluoroethyl]-4-[6-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]-;(S)-N-(1-cyclopropyl-2,2,2-trifluoroethyl)-4-(6-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl)thiophene-2-carboxamide;Unc-51 like kinase,ULK-101,ULK,ULK 101,Inhibitor,ULK101,inhibit;ULK-101, 10 mM in DMSO | | CAS: | 2443816-45-1 | | MF: | C22H16F4N4OS | | MW: | 460.45 | | EINECS: | | | Product Categories: | api | | Mol File: | 2443816-45-1.mol | ![2-Thiophenecarboxamide, N-[(1S)-1-cyclopropyl-2,2,2-trifluoroethyl]-4-[6-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]- Structure](CAS/20200611/GIF/2443816-45-1.gif) |
| | 2-Thiophenecarboxamide, N-[(1S)-1-cyclopropyl-2,2,2-trifluoroethyl]-4-[6-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]- Chemical Properties |
| storage temp. | -10 to -25°C | | solubility | DMSO: 2mg/mL, clear | | form | Solid | | color | Light yellow to yellow | | InChI | 1S/C22H16F4N4OS/c23-16-5-3-12(4-6-16)15-8-27-20-17(9-28-30(20)10-15)14-7-18(32-11-14)21(31)29-19(13-1-2-13)22(24,25)26/h3-11,13,19H,1-2H2,(H,29,31)/t19-/m0/s1 | | InChIKey | PFZRXJIYAFANHP-IBGZPJMESA-N | | SMILES | FC(F)(F)[C@H](C1CC1)NC(C2=CC(C3=C4N(N=C3)C=C(C5=CC=C(C=C5)F)C=N4)=CS2)=O |
| WGK Germany | WGK 3 | | Storage Class | 11 - Combustible Solids |
| | 2-Thiophenecarboxamide, N-[(1S)-1-cyclopropyl-2,2,2-trifluoroethyl]-4-[6-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]- Usage And Synthesis |
| Uses | ULK-101 is a potent and selective ULK1 inhibitor, with IC50 values of 1.6 nM and 30 nM for ULK1 and ULK2, respectively. ULK-101 suppresses autophagy and sensitizes cancer cells to nutrient stress[1]. | | Biological Activity | ULK-101 is a potent and selective ULK1 inhibitor with IC50 values of 8.3 nM and 30 nM for ULK1 and ULK2, respectively. | | in vitro | ULK-101 inhibited the induction of autophagy and autophagic flux under different stimuli. ULK-101 sensitizes KRAS-mutated lung cancer cells to nutrient stress. | | target | | Target | Value | ULK1 (Cell-free assay) | 8.3 nM | ULK2 (Cell-free assay) | 30 nM |
| | IC 50 | ULK1: 1.6 nM (IC50); ULK2: 30 nM (IC50) | | References | [1] Martin KR, et al. A Potent and Selective ULK1 Inhibitor Suppresses Autophagy and Sensitizes Cancer Cells to Nutrient Stress. iScience. 2018 Oct 26;8:74-84. DOI:10.1016/j.isci.2018.09.012 |
| | 2-Thiophenecarboxamide, N-[(1S)-1-cyclopropyl-2,2,2-trifluoroethyl]-4-[6-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl]- Preparation Products And Raw materials |
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