WARNING: This product is for research use only, not for human or veterinary use.
Hodoodo CAT#: H130582
CAS#: DC_M01_7
Description: DC_M01_7 is a novel inhibitor of human histone acetyltransferase KAT8 (also known as MOF or MYST1) with an IC50 value of 6 μM. It significantly inhibits HCT116 cells proliferation and also inhibiting histone 4 lysine 16 acetylation in HCT116 cells.
Hodoodo Cat#: H130582
Name: DC_M01_7
CAS#: DC_M01_7
Chemical Formula: C19H20N2O2S2
Exact Mass: 372.10
Molecular Weight: 372.500
Elemental Analysis: C, 61.26; H, 5.41; N, 7.52; O, 8.59; S, 17.21
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Synonym: DC M01 7, DC-M01-7, DCM017, DC M01-7, DC_M01 7, DC M01_7
IUPAC/Chemical Name: (E)-4-(2-(Benzo[d]thiazol-2-yl)vinyl)-N,N-diethylbenzenesulfonamide
InChi Key: IYTCMWSUAKFEFW-SDNWHVSQSA-N
InChi Code: InChI=1S/C19H20N2O2S2/c1-3-21(4-2)25(22,23)16-12-9-15(10-13-16)11-14-19-20-17-7-5-6-8-18(17)24-19/h5-14H,3-4H2,1-2H3/b14-11+
SMILES Code: O=S(C(C=C1)=CC=C1/C=C/C(S2)=NC3=C2C=CC=C3)(N(CC)CC)=O
Appearance: To be determined
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: To be determined
Shelf Life: >2 years if stored properly
Drug Formulation: To be determined
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:
Biological target: | |
In vitro activity: | |
In vivo activity: |
The following data is based on the product molecular weight 372.50 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.
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: | |
In vitro protocol: | |
In vivo protocol: |
1. Zhang R, Wang J, Zhao L, Liu S, Du D, Ding H, Chen S, Yue L, Liu YC, Zhang C, Liu H, Luo C. Identification of novel inhibitors of histone acetyltransferase hMOF through high throughput screening. Eur J Med Chem. 2018 Sep 5;157:867-876. doi: 10.1016/j.ejmech.2018.08.026. Epub 2018 Aug 17. PMID: 30145373.