KH7
CAS No. 330676-02-3
KH7 ( KH-7;KH 7;sAC inhibitor KH7 )
Catalog No. M14099 CAS No. 330676-02-3
A potent, specific soluble adenylyl cyclase (sAC) inhibitor that inhibits Mn2+-dependent sAC with IC50 of 2.7 uM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 45 | Get Quote |
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5MG | 74 | Get Quote |
|
10MG | 119 | Get Quote |
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25MG | 239 | Get Quote |
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100MG | Get Quote | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
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Biological Information
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Product NameKH7
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NoteResearch use only, not for human use.
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Brief DescriptionA potent, specific soluble adenylyl cyclase (sAC) inhibitor that inhibits Mn2+-dependent sAC with IC50 of 2.7 uM.
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DescriptionA potent, specific soluble adenylyl cyclase (sAC) inhibitor that inhibits Mn2+-dependent sAC with IC50 of 2.7 uM; inhibits physiologically stimulated sAC with similar potency with IC50 of 8.0 uM, completely blocks the capacitation-induced rise in cAMP in wild-type sperm at 10 uM, inhibits in vitro fertilization.
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SynonymsKH-7;KH 7;sAC inhibitor KH7
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PathwayMetabolic Enzyme/Protease
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TargetAdenylate Cyclase
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RecptorAdenylate Cyclase
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Research Area——
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Indication——
Chemical Information
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CAS Number330676-02-3
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Formula Weight419.30
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Molecular FormulaC17H15BrN4O2S
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Purity>98% (HPLC)
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SolubilityDMSO : ≥ 100 mg/mL 238.49 mM; H2O : < 0.1 mg/mL
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SMILESCC(SC1=NC2=CC=CC=C2N1)C(N/N=C/C3=CC(Br)=CC=C3O)=O
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Chemical Name(E)-2-((1H-benzo[d]imidazol-2-yl)thio)-N'-(5-bromo-2-hydroxybenzylidene)propanehydrazide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Bitterman JL, et al. J Pharmacol Exp Ther. 2013 Dec;347(3):589-98.
2. Hess KC, et al. Dev Cell. 2005 Aug;9(2):249-59.
2. Hess KC, et al. Dev Cell. 2005 Aug;9(2):249-59.
molnova catalog
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