CP-060
CAS No. 180090-15-7
CP-060( —— )
Catalog No. M32859 CAS No. 180090-15-7
CP-060 is a potent Ca2+ antagonist and inhibits Ca2+ overload with antioxidant and cardioprotective activities.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 907 | Get Quote |
|
| 5MG | 1131 | Get Quote |
|
| 10MG | 1520 | Get Quote |
|
| 25MG | 2199 | Get Quote |
|
| 50MG | 2962 | Get Quote |
|
| 100MG | 3915 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameCP-060
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NoteResearch use only, not for human use.
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Brief DescriptionCP-060 is a potent Ca2+ antagonist and inhibits Ca2+ overload with antioxidant and cardioprotective activities.
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DescriptionCP- 060 is a potent Ca2+ antagonist, inhibits Ca2+ overload and possesses antioxidant and cardioprotective activities.
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In VitroCP-?060 (0.5, 5 μM) inhibits rabbit LDL oxidation induced by soybean lipoxygenase by 12.9% and 3.0%, respectively.
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In VivoCP-?060 (100 mg/kg, i.v.) increases the coronary blood flow by 96% in anesthetized dogs.
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Synonyms——
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PathwayGPCR/G Protein
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TargetCalcium Channel
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RecptorCalcium Channel
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Research Area——
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Indication——
Chemical Information
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CAS Number180090-15-7
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Formula Weight542.73
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Molecular FormulaC30H42N2O5S
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Purity>98% (HPLC)
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Solubility——
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SMILESC(CCN(CCOC=1C=C2C(=CC1)OCO2)C)N3C(C4=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C4)SCC3=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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TPC2-A1-P
TPC2-A1-P is a membrane-permeable two-pore channel 2 (TPC2) agonist that differentially activates two-pore channel 2 (TPC2) and mimics the activation of TPC2 with NAADP and PIP(2). TPC2-A1-P can be used to study neurodegenerative lysosomal storage diseases.
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Flosatidil
Flosatidil is a small molecule voltage-gated calcium channel complex (VDCCs) blocker for the treatment of neurological disorders and cardiovascular diseases, and can be used in the study of angina pectoris.
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CALP3
Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site. Activates phosphodiesterase in the absence of Ca2+ and inhibits Ca2+-mediated cytotoxicity and apoptosis (IC50 = 33 μM).
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