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524403
Sigma-AldrichPravastatin, Sodium Salt - CAS 81131-70-6 - Calbiochem
A water-soluble, competitive 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor that potently blocks in vivo cholesterol synthesis (Ki = ~1 nM).
More>>A water-soluble, competitive 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor that potently blocks in vivo cholesterol synthesis (Ki = ~1 nM). Less<<
MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
A water-soluble, competitive 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor that potently blocks in vivo cholesterol synthesis (Ki = ~1 nM). Offers cardioprotection. Also acts as an immunomodulator and an inhibitor of ras p21 isoprenylation.
Catalogue Number
524403
Brand Family
Calbiochem®
Synonyms
(βR,δR,1S,2S,6S,8S,8aR)-1,2,6,7,8,8a-Hexahydro-β,δ,6-trihydroxy-2-methyl-8[(2S)-2-methyl-1-oxobutoxyl]-1-naphthaleneheptanoic Acid Na, 3β-Hydroxycompactin, Na
References
References
Kwak, B., et al. 2000. Natl. Med.6, 1399. Hamelin, B.A., and Turgeon, J., 1998. Trends Pharmacol. Sci.19, 26. Narisawa, T., et al. 1996. Jpn. J. Cancer Res.87, 798. Cohen, L.H., et al. 1993. Biochem. Pharmacol.45, 2203. Koga, T., et al. 1990. Biochim. Biophys. Acta.1045, 115. Yoshino, G., et al. 1986. Diabetes Res. Clin. Pract. 2, 179
~1 nM inhibiting 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase and blocking in vivo cholesterol synthesis
Purity
≥98% by HPLC
Physicochemical Information
Cell permeable
N
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
RTECS
QJ7185000
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code
Ambient Temperature Only
Toxicity
Environmental Hazard
Hazardous Materials Attention:
Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
Storage
+2°C to +8°C
Hygroscopic
Hygroscopic
Do not freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Packaged under inert gas
Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
产品目录编号
GTIN
524403-25MGCN
04055977270983
Documentation
Pravastatin, Sodium Salt - CAS 81131-70-6 - Calbiochem MSDS
Pravastatin, Sodium Salt - CAS 81131-70-6 - Calbiochem 分析证书
标题
批号
524403
参考
参考信息概述
Kwak, B., et al. 2000. Natl. Med.6, 1399. Hamelin, B.A., and Turgeon, J., 1998. Trends Pharmacol. Sci.19, 26. Narisawa, T., et al. 1996. Jpn. J. Cancer Res.87, 798. Cohen, L.H., et al. 1993. Biochem. Pharmacol.45, 2203. Koga, T., et al. 1990. Biochim. Biophys. Acta.1045, 115. Yoshino, G., et al. 1986. Diabetes Res. Clin. Pract. 2, 179
数据表
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
16-May-2008 RFH
Synonyms
(βR,δR,1S,2S,6S,8S,8aR)-1,2,6,7,8,8a-Hexahydro-β,δ,6-trihydroxy-2-methyl-8[(2S)-2-methyl-1-oxobutoxyl]-1-naphthaleneheptanoic Acid Na, 3β-Hydroxycompactin, Na
Description
A water-soluble, competitive 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor that blocks in vivo cholesterol synthesis (Ki ~1 nM). Also acts as an immunomodulator and an inhibitor of ras p21 isoprenylation.
Form
White crystalline solid
Intert gas (Yes/No)
Packaged under inert gas
CAS number
81131-70-6
RTECS
QJ7185000
Chemical formula
C₂₃H₃₅O₇.Na
Structure formula
Purity
≥98% by HPLC
Solubility
H₂O (100 mg/ml)
Storage
+2°C to +8°C
Hygroscopic
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity
Environmental Hazard
Merck USA index
14, 7714
References
Kwak, B., et al. 2000. Natl. Med.6, 1399. Hamelin, B.A., and Turgeon, J., 1998. Trends Pharmacol. Sci.19, 26. Narisawa, T., et al. 1996. Jpn. J. Cancer Res.87, 798. Cohen, L.H., et al. 1993. Biochem. Pharmacol.45, 2203. Koga, T., et al. 1990. Biochim. Biophys. Acta.1045, 115. Yoshino, G., et al. 1986. Diabetes Res. Clin. Pract. 2, 179