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Buthionine sulfoximine hydrochlorideDL Buthionine (S, R) sulfoximine hydrochloride (Buthionine sulfoximine hydrochloride) is a potent inhibitor of glutamylcysteine synthetase biosynthesis. Product information Molecular Weight: 258. 77 Formula: C8H19ClN2O3S Chemical Name: 2 amino 4 [butyl(imino)oxo sulfanyl]butanoic acid hydrochloride Smiles: Cl. CCCCS(=N)(=O)CCC(N)C(O)=O InChiKey: FMWPIVFRJOQKNQ UHFFFAOYSA N InChi: InChI=1S C8H18N2O3S. ClH c1 2 3 5 14(10,13)6 4 7(9)8(11)12; h7,10H,2
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DL-Buthionine-(S, R)-sulfoximine hydrochloride (Buthionine sulfoximine hydrochloride) is a potent inhibitor of glutamylcysteine synthetase biosynthesis.

Product information

Molecular Weight: 258.77

Formula: C8H19ClN2O3S

Chemical Name: 2-amino-4-[butyl(imino)oxo--sulfanyl]butanoic acid hydrochloride

Smiles: Cl.CCCCS(=N)(=O)CCC(N)C(O)=O

InChiKey: FMWPIVFRJOQKNQ-UHFFFAOYSA-N

InChi: InChI=1S/C8H18N2O3S.ClH/c1-2-3-5-14(10,13)6-4-7(9)8(11)12;/h7,10H,2-6,9H2,1H3,(H,11,12);1H

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Solubility: H2O : ≥ 140 mg/mL (541.02 mM) DMSO : ≥ 125 mg/mL (483.05 mM) Ethanol : 25 mg/mL (96.61 mM; Need ultrasonic)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥360 days if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

Buthionine sulfoximine is an analogs of methionine sulfoximine and inhibits gamma-glutamylcysteine synthetase about 20 times more effectively than prothionine sulfoximine and at least 100 times more effectively than methionine sulfoximine.

In Vivo:

Treatment of mice bearing HT1080 and HT1080/DR4 xenografts with a continuous i.v infusion of nontoxic doses of D, L-Buthionine-(S, R)-sulfoximine (300 and 600 mg/kg/day) produce a 60% reduction of GSH plasma levels and greater than 95 % reduction in GSH tumor levels in both parental and multidrug-resistant tumors.

References:

  1. Griffith OW, et al. Potent and specific inhibition of glutathione synthesis by buthionine sulfoximine (S-n-butyl homocysteine sulfoximine). J Biol Chem. 1979 Aug 25;254(16):7558-60.
  2. Vanhoefer U, et al. d,l-buthionine-(S,R)-sulfoximine potentiates in vivo the therapeutic efficacy of doxorubicin against multidrug resistance protein-expressing tumors. Clin Cancer Res. 1996 Dec;2(12):1961-8.

Products are for research use only. Not for human use.

Buthionine sulfoximine hydrochloride

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