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Ulixertinib hydrochloride

CAS No.
1956366-10-1
Chemical Name:
Ulixertinib hydrochloride
Synonyms
BVD523;Ulixertinib HCl;Ulixertinib HCl salt;VRT752271 hydrochloride);Ulixertinib hydrochloride;Ulixertinib hydrochloride (BVD-523 hydrochloride;Ulixertinib hydrochloride (Synonyms: BVD-523 hydrochloride;ULIXERTINIB HYDROCHLORIDE (SYNONYMS: BVD-523 HYDROCHLORIDE; VRT752271 HYDROCHLORIDE);(S)-4-(5-chloro-2-(isopropylamino)pyridin-4-yl)-N-(1-(3-chlorophenyl)-2-hydroxyethyl)-1H-pyrrole-2-carboxamidehydrochloride
CBNumber:
CB53133892
Molecular Formula:
C21H23Cl3N4O2
Molecular Weight:
469.79192
MDL Number:
MOL File:
1956366-10-1.mol
Last updated:2024-06-27 13:19:16

Ulixertinib hydrochloride Properties

Melting point 231-232°C
storage temp. -20°C Freezer
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
color White to Off-White
InChIKey DKGYQCPFBWFTHM-JHTMQSDJNA-N
SMILES O=C(N[C@H](CO)C1C=C(Cl)C=CC=1)C1NC=C(C2C(Cl)=CN=C(NC(C)C)C=2)C=1.Cl |&1:3,r|
FDA UNII 3K792HRQ8B

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
HS Code  2933998090
NFPA 704
0
2 0

Ulixertinib hydrochloride price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 18298 Ulixertinib (hydrochloride) ≥98% 1956366-10-1 1mg $29 2024-03-01 Buy
Cayman Chemical 18298 Ulixertinib (hydrochloride) ≥98% 1956366-10-1 5mg $64 2024-03-01 Buy
Cayman Chemical 18298 Ulixertinib (hydrochloride) ≥98% 1956366-10-1 10mg $99 2024-03-01 Buy
Cayman Chemical 18298 Ulixertinib (hydrochloride) ≥98% 1956366-10-1 25mg $141 2024-03-01 Buy
TRC U700835 UlixertinibHydrochloride 1956366-10-1 250mg $345 2021-12-16 Buy
Product number Packaging Price Buy
18298 1mg $29 Buy
18298 5mg $64 Buy
18298 10mg $99 Buy
18298 25mg $141 Buy
U700835 250mg $345 Buy

Ulixertinib hydrochloride Chemical Properties,Uses,Production

Configuration method

Ulixertinib (hydrochloride) is supplied as a crystalline solid. A stock solution may be made by dissolving the ulixertinib (hydrochloride) in the solvent of choice, which should be purged with an inert gas. Ulixertinib (hydrochloride) is soluble in organic solvents such as ethanol, DMSO, and dimethylformamide (DMF). The solubility of this compound in ethanol is approximately 1 mg/ml and approximately 30 mg/ml in DMSO and DMF. Ulixertinib(hydrochloride) is sparingly soluble in aqueous buffers. For maximum solubility in aqueous buffers,ulixertinib (hydrochloride) should first be dissolved in DMSO and then diluted with the aqueous buffer of choice. Ulixertinib (hydrochloride) has a solubility of approximately 0.25 mg/ml in a 1:3 solution of DMSO: PBS (pH 7.2) using this method.

Description

Ulixertinib is a reversible ERK1/2 inhibitor that demonstrates an IC50 value of <0.3 nM for ERK2. In A375 melanoma cells with b-RafV600E mutation, it has been reported to reduce the levels of phosphorylated ERK2 and the downstream kinase RSK (IC50s = 4.1 and 0.14 μM, respectively). Ulixertinib has also been shown to inhibit A375 cell proliferation with an IC50 value of 180 nM.

Uses

Ulixertinib Hydrochloride is an acid salt of Ulixertinib (U700830), a potent and reversible ERK1/ERK2 inhibitor with IC50 of <0.3 nM for ERK2. Inhibits cell proliferation. Anti-cancer.

Uses

Ulixertinib hydrochloride is a potent in vitro inhibitor of ERK1/2 kinase that contacts myogenic precursor cells in farmed animals, thereby promoting fusion and myogenic maturation for industrial meat production.

in vitro

in two lymphoma cell lines (sudhl-10 and raji), treatment with ulixertinib significantly reduced the expression of erk1/2 phosphorylation in a dose-dependent manner. treatment with 0.4 nm ulixertinib decreased the percentage of g2-m phase cells in the sudhl-10 cells. in the raji cells, treated with ulixertinib at 0.4 and 1.0 nm increased the percentage of g0-g1 phase cells and decreased s phase cells [1]. treatment of ulixertinib at the dose of 0.1, 0.4 and 1.0 nm for 48 h dose-dependently increased the number of early apoptotic sudhl- 10 and raji cells [1]. in sudhl-10 and raji cells, ulixertinib reduced mrna and protein expression of vegfr2 and bcl-2 genes and increased the expression of bax and caspase-3 genes [1].

in vivo

bvd-523 inhibited tumor growth in braf-mutant melanoma and colorectal xenografts as well as in kras-mutant colorectal and pancreatic models. bvd-523 treatment in combination with dabrafenib inhibited tumor growth in a braf-mutant melanoma model [3]. single-agent bvd-523 inhibited the growth of a patient-derived tumor xenograft harboring cross-resistance to dabrafenib, trametinib, and the combination treatment following clinical progression on a mek inhibitor [3].

Ulixertinib hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 46)Suppliers
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Wuhan Jingkang en Biomedical Technology Co., Ltd
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ATK CHEMICAL COMPANY LIMITED
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Amadis Chemical Company Limited
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Kaixin Chemical (Hong Kong) Limited 010-88886666-01 13112345678 loyson@tcypharm.com China 595 55

Ulixertinib hydrochloride Spectrum

BVD523 (S)-4-(5-chloro-2-(isopropylamino)pyridin-4-yl)-N-(1-(3-chlorophenyl)-2-hydroxyethyl)-1H-pyrrole-2-carboxamidehydrochloride Ulixertinib hydrochloride Ulixertinib HCl salt Ulixertinib HCl Ulixertinib hydrochloride (BVD-523 hydrochloride VRT752271 hydrochloride) Ulixertinib hydrochloride (Synonyms: BVD-523 hydrochloride ULIXERTINIB HYDROCHLORIDE (SYNONYMS: BVD-523 HYDROCHLORIDE; VRT752271 HYDROCHLORIDE) 1956366-10-1