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  3. JZP-430

JZP-430 

Cat. No.: HY-101457 Purity: >99.0%
Handling Instructions

JZP-430 is a potent, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) with an IC50 of 44 nM, exhibits ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).

For research use only. We do not sell to patients.

JZP-430 Chemical Structure

JZP-430 Chemical Structure

CAS No. : 1672691-74-5

Size Price Stock Quantity
10 mM * 1 mL in DMSO USD 308 In-stock
Estimated Time of Arrival: December 31
5 mg USD 280 In-stock
Estimated Time of Arrival: December 31
10 mg   Get quote  
50 mg   Get quote  

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Description

JZP-430 is a potent, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) with an IC50 of 44 nM, exhibits ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL)[1].

IC50 & Target

IC50: 44 nM (ABHD6, human)[1]

Storage
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
References
Molecular Weight

354.47

Formula

C₁₆H₂₆N₄O₃S

CAS No.

1672691-74-5

SMILES

O=C(OC1=NSN=C1N2CCOCC2)N(C3CCCCCCC3)C

Shipping

Room temperature in continental US; may vary elsewhere

Purity: >99.0%

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This equation is commonly abbreviated as: C1V1 = C2V2

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Product Name:
JZP-430
Cat. No.:
HY-101457
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JZP-430

Cat. No.: HY-101457