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Chemical Structure| 1030203-81-6 Chemical Structure| 1030203-81-6

Structure of HS38
CAS No.: 1030203-81-6

Chemical Structure| 1030203-81-6

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HS38 is a potent inhibitor of DAPK1 and ZIPK, with Kd values of 300 nM and 280 nM, respectively, suitable for research on smooth muscle diseases and related pathologies, with potential therapeutic applications.

Synonyms: HS38

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Product Details of HS38

CAS No. :1030203-81-6
Formula : C14H12ClN5O2S
M.W : 349.80
SMILES Code : CC(SC1=NC(N(C2=CC=CC(Cl)=C2)N=C3)=C3C(N1)=O)C(N)=O
Synonyms :
HS38
MDL No. :MFCD10610687
InChI Key :NASYEGAVCTZSDO-UHFFFAOYSA-N
Pubchem ID :135398509

Safety of HS38

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Isoform Comparison

Biological Activity

Description
HS38 is a potent, selective, and ATP-competitive inhibitor, targeting death-associated protein kinase 1 (DAPK1) and zipper-interacting protein kinase (ZIPK or DAPK3) with dissociation constants (Kds) of 300 nM and 280 nM, respectively. Additionally, it acts as a PIM3 inhibitor with an IC50 of 200 nM, showing potential for smooth muscle related disorder research[1].

In Vitro:

Cell Line
Concentration Treated Time Description References
human detrusor tissues 3 µM 30 minutes To assess the effects of HS38 on carbachol-induced contractions. Results showed that HS38 did not affect contractions. Naunyn Schmiedebergs Arch Pharmacol. 2024 Feb;397(2):1219-1231
porcine interlobar arteries 3 µM 30 minutes To assess the effects of HS38 on noradrenaline-, phenylephrine-, and methoxamine-induced contractions. Results showed that HS38 partially but inconsistently reduced contractions. Naunyn Schmiedebergs Arch Pharmacol. 2024 Feb;397(2):1219-1231
human prostate tissues 3 µM 30 minutes To assess the effects of HS38 on noradrenaline-, phenylephrine-, and methoxamine-induced contractions. Results showed that HS38 partially but inconsistently reduced contractions. Naunyn Schmiedebergs Arch Pharmacol. 2024 Feb;397(2):1219-1231
human coronary artery vascular smooth muscle cells (CASMCs) 50 μM Evaluate the effect of HS38 on cofilin phosphorylation, results showed no significant effect of HS38 on cofilin phosphorylation Sci Rep. 2016 Aug 30;6:32118
Coronary artery smooth muscle cells (CASMCs) 50 μM 16 hours To investigate the effects of HS38 on the cytoskeletal architecture and FAK phosphorylation status of vascular smooth muscle cells. Results showed that HS38 treatment significantly altered F-actin cytoskeletal organization and reduced pY397-FAK phosphorylation levels. Exp Physiol. 2023 Jul;108(7):986-997

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Sprague-Dawley rats Posterior cerebral artery (PCA) vessel model Ex vivo perfusion 10 μM Single administration, lasting 30 minutes To evaluate the inhibitory effect of HS38 on the myogenic response of posterior cerebral arteries. Results demonstrated that HS38 significantly attenuated vessel constrictions invoked by serotonin and intraluminal pressure elevation, and this dilatation was not associated with any change in myosin light chain (LC20) phosphorylation. Exp Physiol. 2023 Jul;108(7):986-997

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.86mL

0.57mL

0.29mL

14.29mL

2.86mL

1.43mL

28.59mL

5.72mL

2.86mL

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