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VU0456810

CAS No.
1443246-62-5
Chemical Name:
VU0456810
Synonyms
ML297;VU0456810;CID 56642816;ML297 (VU0456810);ML297 >=98% (HPLC);ML297, Pubchem: CID 56642816;ML 297 (Synonyms: VU 0456810;ML 297;ML-297;ML297;VU0456810;VU-0456810;VU 0456810;GIRK Activator, ML297 - CAS 1443246-62-5 - Calbiochem;1-(3,4-DIFLUOROPHENYL)-3-(5-METHYL-2-PHENYLPYRAZOL-3-YL)UREA
CBNumber:
CB22750693
Molecular Formula:
C17H14F2N4O
Molecular Weight:
328.32
MDL Number:
MFCD27977571
MOL File:
1443246-62-5.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

VU0456810 Properties

Boiling point 377.8±42.0 °C(Predicted)
Density 1.32±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility DMSO: soluble15mg/mL, clear
pka 12.54±0.70(Predicted)
form White powder
color white to beige
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS09
Signal word  Warning
Hazard statements  H410
Precautionary statements  P273-P501
Hazard Codes  N
Risk Statements  50/53
Safety Statements  60-61
RIDADR  UN 3077 9 / PGIII
WGK Germany  3

VU0456810 price More Price(28)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML0836 ML297 ≥98% (HPLC) 1443246-62-5 5mg $118 2024-03-01 Buy
Sigma-Aldrich SML0836 ML297 ≥98% (HPLC) 1443246-62-5 25mg $479 2024-03-01 Buy
Sigma-Aldrich 5.05820 GIRK Activator, ML297 - CAS 1443246-62-5 - Calbiochem 1443246-62-5 10mg $230 2022-05-15 Buy
Cayman Chemical 14792 ML-297 ≥98% 1443246-62-5 1mg $49 2024-03-01 Buy
Cayman Chemical 14792 ML-297 ≥98% 1443246-62-5 5mg $216 2024-03-01 Buy
Product number Packaging Price Buy
SML0836 5mg $118 Buy
SML0836 25mg $479 Buy
5.05820 10mg $230 Buy
14792 1mg $49 Buy
14792 5mg $216 Buy

VU0456810 Chemical Properties,Uses,Production

Description

ML297 (1443246-62-5) is a selective GIRK 1/2 (Kir3.1/3.2) channel activator, IC50?= 160, 887 and 914 nM for GIRK1/2, GIRK1/4 and GIRK1/3 respectively. Has no effect on GIRK2, GIRK2/3, Kir2.1 and Kv7.4 channels.1,2??Displays antiseizure activity2?and decreases anxiety-related behavior without sedative or addictive effects3. Reduces glucose- and IBMX-stimulated GLP-1 secretion with no effect on GIP in murine L and K cells.4?Brain penetrant.

Uses

ML 297 is an anxiolytic drug which acts as a selective Kir3.1/3.2 (GIRK1/2) channel activator. It may be used in the treatment of epileptic seizures.

in vitro

in thallium flux assays, ml297 showed concentration-dependent efficacy when tested on cells expressing girk1/2. ml297 could also activate girk channels comprised of girk1/3 and girk1/4 subunit combinations. however, ml297 diaplayed a complete inability to modulate the activity of hek-293 cells expressing girk2 alone. a similar complete lack of efficacy was seen when ml297 was tested on hek-293 cells expressing girk2/3. therefore, it appeared that ml297 is only capable of activating girk channels containing a girk1 subunit [1].

in vivo

previous study performed an ascending dose study in mice and it was found that the animals appeared normal and not under obvious distress at all doses tested. ml297’s effects on locomotor activity as well as effects on motor function and coordination were further evaluated. results showed that ml297 at 60 mg/kg could immediate decrease in locomotor activity compared to the control group [1].

storage

Store at -20°C

References

1) Wen?et al.?(2014),?Discovery of potent and selective GIRK1/2 modulators via “molecular switches’ within a series of 1-(3-cyclopropyl-1-phenyl-1H-pyrazol-5-yl)ureas; Bioorg. Med. Chem. Lett.,?24?5102 2) Kaufmann?et al. (2013),?ML-297 (VU0456810), the first potent and selective activator of the GIRK potassium channel, displays antiepileptic properties in mice; ACS Chem. Neurosci.,?4?1278 3) Wydeven?et al.?(2014),?Mechanisms underlying the activation of G-protein-gated inwardly rectifying K+ (GIRK) channels by the novel anxiolytic drug, ML297; Proc. Natl. Acad. Sci. USA,?111?10755 4) Psichas?et al.?(2016),?Galanin inhibits GLP-1 and GIP secretion via the GAL1 receptor in enteroendocrine L and K cells; Br. J. Pharmacol.,?173?888

VU0456810 Preparation Products And Raw materials

Raw materials

Preparation Products

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1-(3,4-Difluorophenyl)-3-(3-methyl-1-phenyl-1H-pyrazol-5-yl)urea CID 56642816 ML297 VU0456810 1-(3,4-DIFLUOROPHENYL)-3-(5-METHYL-2-PHENYLPYRAZOL-3-YL)UREA ML297, Pubchem: CID 56642816 ML297 (VU0456810) ML 297;ML-297;ML297;VU0456810;VU-0456810;VU 0456810 GIRK Activator, ML297 - CAS 1443246-62-5 - Calbiochem ML 297 (Synonyms: VU 0456810 Urea, N-(3,4-difluorophenyl)-N'-(3-methyl-1-phenyl-1H-pyrazol-5-yl)- ML297 >=98% (HPLC) CID 56642816,epilepsy,GIRK1/2,Potassium Channel,CID56642816,VU0456810,CID-56642816,GIRK,ML-297,convulsions,inhibit,KcsA,ML 297,VU-0456810,VU 0456810,Inhibitor 1443246-62-5