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Cat. No.: HY-189686

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SHC 1

SHC 1 is a dual HDAC8/HDAC6 inhibitor (HDAC8: IC₅₀ = 0.036 μM; HDAC6: IC₅₀ = 1.7 μM) that increases SMC3 acetylation levels. SHC 1 inhibits neuroblastoma cell proliferation, colony formation, and migration, induces caspase 3/7 activity, and exhibits antiproliferative activity against neuroblastoma cells superior to that against normal cells. SHC 1 can be used for research on neuroblastoma.

Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.

Formule: C₁₁H₉N₃S₄
Masse moléculaire:311.47

Stockage:

Please store the product under the recommended conditions in the Certificate of Analysis.

SHC 1 Chemical Structure

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Amount: USD 0.00

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Activité biologique
- Description
- IC₅₀ & Target
- Cellular Effect
- In Vitro
Chemical Information
Pureté et documentation
Références
Calculators
Help & FAQs
Classifications
Bioz

Activité biologique

Description

IC₅₀ & Target

^[1]

HDAC8

0.036 μM (IC₅₀)

hHDAC6

1.7 μM (IC₅₀)

Caspase-3

Caspase-7

Voir tous les produits spécifiques à Isoform HDAC :

Voir tous les produits spécifiques à Isoform Caspase :

Cellular Effect

Cell Line	Type	Value	Description	References
IMR-32	IC50	16.55 μM	Antiproliferative activity against human IMR-32 neuroblastoma cells assessed as viability reduction by MTT assay. Antiproliferative activity against human IMR-32 neuroblastoma cells assessed as viability reduction by MTT assay.	42767177
HCT-116	IC50	38.695 μM	Antiproliferative activity against human HCT-116 colorectal carcinoma cells assessed as viability reduction by MTT assay. Antiproliferative activity against human HCT-116 colorectal carcinoma cells assessed as viability reduction by MTT assay.	42767177
MCF7	IC50	46.405 μM	Antiproliferative activity against human MCF-7 breast adenocarcinoma cells assessed as viability reduction by MTT assay. Antiproliferative activity against human MCF-7 breast adenocarcinoma cells assessed as viability reduction by MTT assay.	42767177
HEK293	IC50	41.05 μM	Cytotoxicity against normal human HEK-293 cells assessed as viability reduction by MTT assay. Cytotoxicity against normal human HEK-293 cells assessed as viability reduction by MTT assay.	42767177

In Vitro

Anti-cancerApoptosisOthers

Anti-cancer

SHC-1 inhibits IMR-32 neuroblastoma cell proliferation with an IC₅₀ of 16.55 μM and exhibits moderate selectivity toward HEK-293 cells (SI 2.480)^[1].
SHC-1 (5 μM; 9-12 days) and SHC-2 (10 μM; 9-12 days) reduce colony formation of IMR-32 neuroblastoma cells^[1].
SHC-1 (5 μM; 48 h) and SHC-2 (10 μM; 48 h) inhibit the migration of IMR-32 neuroblastoma cells^[1].

Apoptosis

SHC-1 (5-10 μM) increases caspase-3/7 activity by approximately 1.45-fold at 5 μM and 2-fold at 10 μM, supporting its pro-apoptotic effect^[1].

Others

SHC-1 inhibits HDAC8 with an IC₅₀ of 0.036 μM, shows selectivity over HDAC4, HDAC3, HDAC10, and HDAC11 (IC₅₀ > 35 μM), and has weak activity against HDAC1 and HDAC6^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Migration Assay ^[1]

Cell Line:

IMR-32 neuroblastoma cells
Concentration:

5 μM
Incubation Time:

48 h
Result:

Successfully stopped IMR-32 cells from migrating.

Western Blot Analysis^[1]

Cell Line:

IMR-32 neuroblastoma cells
Concentration:

5 μM, 10 μM
Incubation Time:

24 h
Result:

Observed a dose-dependent increase in acetylated SMC3 levels with compounds SHC-1 and SHC-2 relative to total SMC3 levels.

Related Protocols :

Chemical Information

Masse moléculaire 311.47
Formule C₁₁H₉N₃S₄
SMILES

N#C/N=C(SC)\SCSC1=NC(C=CC=C2)=C2S1
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureté et documentation

Instruction de manipulation (2659 KB)

Références

[1]. Kosana SC, et al. Discovery of cyanocarbonimidodithioates as novel non-hydroxamate zinc-binding groups for selective HDAC8 inhibition: Design, synthesis, biological evaluation, anticancer activity, and in silico studies. Bioorganic chemistry. 2026 Sep 17;182:110551.

Calculators

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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MOQ

Minimum order quantity

100 mg

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Activité biologique
- Description
- IC₅₀ & Target
- In Vitro
Chemical Information
Pureté et documentation
Références

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SHC 1

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