Comparison

Ravoxertinib hydrochloride European Partner

Item no. HY-15947A-50mg
Manufacturer MedChem Express
CASRN 2070009-58-2
Amount 50 mg
Quantity options 10 mM/1 mL 10 mg 50 mg 5 mg
Category
Type Inhibitors
Specific against other
Purity 99.44
Citations [1]Blake JF, et al. Discovery of (S)-1-(1-(4-Chloro-3-fluorophenyl)-2-hydroxyethyl)-4-(2-((1-methyl-1H-pyrazol-5-yl)amino)pyrimidin-4-yl)pyridin-2(1H)-one (GDC-0994), an Extracellular Signal-Regulated Kinase 1/2 (ERK1/2) Inhibitor in Early Clinical Developme|[2]Kirk Robarge, et al. Abstract DDT02-03: Discovery of GDC-0994, a potent and selective ERK1/2 inhibitor in early clinical development. Proceedings: AACR Annual Meeting 2014; April 5-9, 2014.|[3]MICHAEL LAI. Opportunity for Pharmaceutical Intervention in Lung Cancer: Selective Inhibition of JAK1/2 to Eliminate EMT-Derived Mesenchymal Cells.
ACS Omega. 2023 May 23.|Nucleic Acids Res. 2022 Apr 8;50(6):3096-3114.|Pathol Res Pract. December 2021, 153682.|ACS Comb Sci. 2019 Dec 9;21(12):805-816.|Am J Cancer Res. 2020 Nov 1;10(11):3622-3643.|Am J Physiol Heart Circ Physiol. 2018 Mar 1;314(3):H580-H592.|Biochem Biophys Res Commun. 2021 Mar 26;554:63-70.|Cancer Cell. 2023 Jul 10;41(7):1345-1362.e9.|Cancer. 2020 Mar 15;126(6):1339-1350.|Cancers (Basel). 2022 Mar 19;14(6):1575.|Cancers (Basel). 2022 May 19;14(10):2493.|Cell Death Dis. 2021 Dec 1;12(12):1123.|Cell Mol Immunol. 2023 Jan 5.|Cell Rep Med. 2025 Feb 6:101970.|Cell Rep. 2023 Sep 1;42(9):113048.|Cell Signal. 2023 Jan 20;110607.|Cell. 2018 Sep 20;175(1):186-199.e19.|Clin Transl Med. 2023 Aug;13(8):e1381.|Diabetes. 2021 Jun 21;db200719.|Environ Pollut. 2021 Jan 1;268(Pt B):115748.|Exp Mol Pathol. 2021 Feb;118:104587.|Gastric Cancer. 2023 Feb 22.|Harvard Medical School LINCS LIBRARY|Indian J Pharm Sci. 2022.|Int J Med Sci. 2022 Jan 1;19(1):195-204.|iScience. 2024 Sep 12;27(10):110873.|J Cell Biochem. 2020 Mar;121(3):2343-2353.|J Cell Mol Med. 2020 Sep;24(17):10151-10165.|J Exp Clin Cancer Res. 2023 Jul 13;42(1):166.|J Pharmacol Exp Ther. 2020 Jul;374(1):104-112.|Methods Mol Biol. 2018;1711:351-398.|Mol Oncol. 2020 Nov;14(11):2894-2919.|Nat Commun. 2023 Sep 30;14(1):6117.|Nat Metab. 2022 Mar;4(3):374-388.|Nature. 2025 Jan;637(8046):726-735. |Neural Regen Res. 2023.|Oncogene. 2021 Jul;40(30):4884-4893.|Proteomics. 2023 May 4;e2300041.|Redox Biol. 2023 Jul 24, 102825.|Reprod Sci. 2020 Feb;27(2):704-712.|Sci Transl Med. 2021 Jan 27;13(578):eaba7308.|Toxicol In Vitro. 2020 Jun;65:104777.|Universität Würzburg. Graduate School of Life Sciences. 2021 Jan.|Université de Lausanne. 2024 Feb 7.|Zool Res. 2022 Jul 18;43(4):537-551.
Smiles O=C1C=C(C2=NC(NC3=CC=NN3C)=NC=C2)C=CN1[C@@H](C4=CC=C(Cl)C(F)=C4)CO.Cl[H]
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias GDC-0994 (hydrochloride)
Shipping Condition Room temperature
Available
Manufacturer - Type
Reference compound
Manufacturer - Applications
Cancer-Kinase/protease
Manufacturer - Targets
ERK
Shipping Temperature
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Molecular Weight
477.32
Product Description
Ravoxertinib hydrochloride (GDC-0994 hydrochloride) is an orally bioavailable inhibitor selective for ERK kinase activity with IC50 of 6.1 nM and 3.1 nM for ERK1 and ERK2, respectively.
Manufacturer - Research Area
Cancer
Solubility
DMSO: 100 mg/mL (ultrasonic)|H2O: < 0.1 mg/mL (ultrasonic; warming; heat to 80°C)
Manufacturer - Pathway
MAPK/ERK Pathway; Stem Cell/Wnt
Isoform
ERK1; ERK2
Clinical information
Phase 1

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 50 mg
Available: In stock
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