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JZP-430

JZP-430
JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
Catalog No. T15635Cas No. 1672691-74-5
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Purity:99.78%
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JZP-430

Catalog No. T15635Cas No. 1672691-74-5

JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
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Pack SizePriceAvailabilityQuantity
1 mg$59In Stock
5 mg$98In Stock
10 mg$158In Stock
25 mg$287In Stock
50 mg$413In Stock
100 mg$592In Stock
200 mg$783In Stock
1 mL x 10 mM (in DMSO)$107In Stock
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Product Introduction

Bioactivity
Description
JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
Targets&IC50
ABHD6:44 nM(Human)
Chemical Properties
Molecular Weight354.47
FormulaC16H26N4O3S
Cas No.1672691-74-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 90 mg/mL (253.9 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8211 mL14.1056 mL28.2111 mL141.0557 mL
5 mM0.5642 mL2.8211 mL5.6422 mL28.2111 mL
10 mM0.2821 mL1.4106 mL2.8211 mL14.1056 mL
20 mM0.1411 mL0.7053 mL1.4106 mL7.0528 mL
50 mM0.0564 mL0.2821 mL0.5642 mL2.8211 mL
100 mM0.0282 mL0.1411 mL0.2821 mL1.4106 mL

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