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EST64454

CAS No.
1950569-11-5
Chemical Name:
EST64454
Synonyms
EST64454;EST64454 HCl;EST64454 hydrochloride;EST64454 hydrochloride, 10 mM in DMSO;pain,Inhibitor,EST 64454,EST64454 hydrochloride,nerve,selective,EST-64454 hydrochloride,Sigma Receptor,EST-64454,oral,inhibit
CBNumber:
CB28210252
Molecular Formula:
C18H23ClF2N4O2
Molecular Weight:
400.85
MDL Number:
MFCD33023223
MOL File:
1950569-11-5.mol
Last updated:2025-04-17 18:22:24

EST64454 Properties

storage temp. Store at -20°C
solubility DMSO : 100 mg/mL (249.47 mM; Need ultrasonic)
form Solid
color White to off-white

EST64454 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0144561 EST64454hydrochloride 99.19% 1950569-11-5 5mg $350 2021-12-16 Buy
ChemScene CS-0144561 EST64454hydrochloride 99.19% 1950569-11-5 10mg $550 2021-12-16 Buy
ChemScene CS-0144561 EST64454hydrochloride 99.19% 1950569-11-5 25mg $950 2021-12-16 Buy
ChemScene CS-0144561 EST64454hydrochloride 99.19% 1950569-11-5 50mg $1450 2021-12-16 Buy
ChemScene CS-0144561 EST64454hydrochloride 99.19% 1950569-11-5 100mg $2250 2021-12-16 Buy
Product number Packaging Price Buy
CS-0144561 5mg $350 Buy
CS-0144561 10mg $550 Buy
CS-0144561 25mg $950 Buy
CS-0144561 50mg $1450 Buy
CS-0144561 100mg $2250 Buy

EST64454 Chemical Properties,Uses,Production

Uses

EST64454 hydrochloride is a selective and orally active sigma-1 receptor antagonist with a Ki of 22 nM. EST64454 hydrochloride has the potential for the research of the pain[1].

Biological Activity

EST64454 hydrochloride is a selective and orally active sigma-1 receptor antagonist with a Ki of 22 nM. EST64454 hydrochloride has the potential for the research of the pain[1]. EST64454 (10 mg/kg; p.o.; male Wistar rats) treatment shows the Cmax, t1/2, AUC0-∞, Vss and F% are 771 ng/mL, 3.4 hours, 1431 ng h/mL, 4.4 l/kg and 69%, respectively[1].EST64454 (10 mg/kg; p.o.; male CD1 mice) treatment shows the Cmax, t1/2, AUC0-∞, Vss and F% were 1178 ng/mL, <1 hours, 2645 ng h/mL, 1.2 l/kg and 60%, respectively[1].

in vivo

EST64454 (10 mg/kg; p.o.; male Wistar rats) treatment shows the Cmax, t1/2, AUC0-∞, Vss and F% are 771 ng/mL, 3.4 hours, 1431 ng h/mL, 4.4 l/kg and 69%, respectively[1].
EST64454 (10 mg/kg; p.o.; male CD1 mice) treatment shows the Cmax, t1/2, AUC0-∞, Vss and F% were 1178 ng/mL, <1 hours, 2645 ng h/mL, 1.2 l/kg and 60%, respectively[1].

Animal Model:Male Wistar rats (250-300 g)[1]
Dosage:10 mg/kg
Administration:P.o. (Pharmacokinetic Analysis)
Result:The Cmax, t1/2, AUC0-∞, Vss and F% were 771 ng/mL, 3.4 hours, 1431 ng h/mL, 4.4 l/kg and 69%, respectively.

References

[1]. Díaz JL, et al. EST64454: a Highly Soluble σ1 Receptor Antagonist Clinical Candidate for Pain Management. J Med Chem. 2020;63(23):14979-14988.

EST64454 Preparation Products And Raw materials

Raw materials

Preparation Products

EST64454 Suppliers

Global( 17)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6391 58
TargetMol Chemicals Inc.
support@targetmol.com United States 38663 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8467 58
Aladdin Scientific
tp@aladdinsci.com United States 52924 58
Shanghai Chaolan Chemical Technology Center 021-QQ:65489617 15618227136 Sales@ATKchemical.com China 9342 58
Wuhan Augda Biotechnology Co., Ltd 15071299552 262933239@qq.com China 6952 58
InvivoChem 13549236410 sales@invivochem.cn China 6753 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24863 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11973 58

EST64454 Spectrum

EST64454 EST64454 hydrochloride EST64454 HCl pain,Inhibitor,EST 64454,EST64454 hydrochloride,nerve,selective,EST-64454 hydrochloride,Sigma Receptor,EST-64454,oral,inhibit EST64454 hydrochloride, 10 mM in DMSO 1950569-11-5