MedKoo Cat#: 555620 | Name: SIS-17
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

SIS-17 is a potent and selective HDAC 11 inhibitor with an IC50 value of 0.83 μM. SIS-17, is active in cells and inhibited the demyristoylation of a known HDAC11 substrate, serine hydroxymethyl transferase 2, without inhibiting other HDACs.

Chemical Structure

SIS-17
CAS#2374313-54-7

Theoretical Analysis

MedKoo Cat#: 555620

Name: SIS-17

CAS#: 2374313-54-7

Chemical Formula: C21H38N2OS

Exact Mass: 366.2705

Molecular Weight: 366.61

Elemental Analysis: C, 68.80; H, 10.45; N, 7.64; O, 4.36; S, 8.75

Price and Availability

Size Price Availability Quantity
10mg USD 150.00 Ready to ship
25mg USD 250.00 Ready to ship
50mg USD 450.00 Ready to ship
100mg USD 750.00 Ready to ship
200mg USD 1,350.00 Ready to ship
500mg USD 2,650.00 Ready to ship
1g USD 3,850.00 Ready to ship
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Related CAS #
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Synonym
SIS-17; SIS 17; SIS17;
IUPAC/Chemical Name
N'-hexadecylthiophene-2-carbohydrazide
InChi Key
HSHXDCVZWHOWCS-UHFFFAOYSA-N
InChi Code
InChI=1S/C21H38N2OS/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18-22-23-21(24)20-17-16-19-25-20/h16-17,19,22H,2-15,18H2,1H3,(H,23,24)
SMILES Code
O=C(C1=CC=CS1)NNCCCCCCCCCCCCCCCC
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Mammalian histone deacetylases (HDACs) are a class of enzymes that play important roles in biological pathways. Existing HDAC inhibitors target multiple HDACs without much selectivity. Inhibitors that target one particular HDAC will be useful for investigating the biological functions of HDACs and for developing better therapeutics.
Biological target:
SIS-17 is a histone deacetylase 11 (HDAC 11) inhibitor with an IC50 value of 0.83 μM.
In vitro activity:
Results from this study indicate that SIS-17 is active in cells and inhibited the demyristoylation of a known HDAC11 substrate, serine hydroxymethyl transferase 2, without inhibiting other HDACs. Reference: ACS Chem Biol. 2019 Jul 19;14(7):1393-1397. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893910/
In vivo activity:
To be determined
Solvent mg/mL mM comments
Solubility
DMSO 99.0 270.04
Ethanol 18.0 49.10
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 366.61 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
1. Li R, Wu X, Zhao P, Xue K, Li J. A pan-cancer analysis identifies HDAC11 as an immunological and prognostic biomarker. FASEB J. 2022 Jul;36(7):e22326. doi: 10.1096/fj.202101742RR. PMID: 35657209. 2. Son SI, Cao J, Zhu CL, Miller SP, Lin H. Activity-Guided Design of HDAC11-Specific Inhibitors. ACS Chem Biol. 2019 Jul 19;14(7):1393-1397. doi: 10.1021/acschembio.9b00292. Epub 2019 Jul 2. PMID: 31264832; PMCID: PMC6893910. In vivo study To be determined
In vitro protocol:
1. Li R, Wu X, Zhao P, Xue K, Li J. A pan-cancer analysis identifies HDAC11 as an immunological and prognostic biomarker. FASEB J. 2022 Jul;36(7):e22326. doi: 10.1096/fj.202101742RR. PMID: 35657209. 2. Son SI, Cao J, Zhu CL, Miller SP, Lin H. Activity-Guided Design of HDAC11-Specific Inhibitors. ACS Chem Biol. 2019 Jul 19;14(7):1393-1397. doi: 10.1021/acschembio.9b00292. Epub 2019 Jul 2. PMID: 31264832; PMCID: PMC6893910.
In vivo protocol:
To be determined
1: Son SI, Cao J, Zhu CL, Miller SP, Lin H. Activity-Guided Design of HDAC11-Specific Inhibitors. ACS Chem Biol. 2019 Jul 19;14(7):1393-1397. doi: 10.1021/acschembio.9b00292. Epub 2019 Jul 2. PubMed PMID: 31264832.