Cart
sales@molnova.com
Home -
Products -
Chromatin/Epigenetic -
Epigenetic Reader Domain -
2-methyl-2,3,4,5-tetrahydro-1,5-benzothiazepin-4-one
2-methyl-2,3,4,5-tetrahydro-1,5-benzothiazepin-4-one
CAS No. 96680-77-2
2-methyl-2,3,4,5-tetrahydro-1,5-benzothiazepin-4-one( —— )
Catalog No. M28385 CAS No. 96680-77-2
2-methyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is ligand of CBP.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 29 | In Stock |
|
| 25MG | 51 | In Stock |
|
| 50MG | 75 | In Stock |
|
| 100MG | 112 | In Stock |
|
| 200MG | 168 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name2-methyl-2,3,4,5-tetrahydro-1,5-benzothiazepin-4-one
-
NoteResearch use only, not for human use.
-
Brief Description2-methyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is ligand of CBP.
-
Description2-methyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is ligand of CBP.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayChromatin/Epigenetic
-
TargetEpigenetic Reader Domain
-
RecptorHuman Endogenous Metabolite|GPR109B|AhR
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number96680-77-2
-
Formula Weight193.26
-
Molecular FormulaC10H11NOS
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCC1CC(=O)Nc2ccccc2S1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Wang XD, et al. A method for the determination of D-kynurenine in biological tissues. Anal Bioanal Chem. 2013 Dec;405(30):9747-54.
molnova catalog
related products
-
PBRM1-BD2-IN-8
PBRM1-BD2-IN-8 (compound 34) is a potent PBRM1 Bromodomain inhibitor with PBRM1-BD2 Kd of 4.4 μM, PBRM1-BD2 IC50 of 0.16 μM, and PBRM1-BD5 Kd of 25 μM; PBRM1-BD2-IN-8 shows anti-cancer activity.
-
3-methyl-1,2-dihydro...
3-methyl-1,2-dihydroquinolin-2-one is the first known micromolar inhibitors of the ATAD2 bromodomain.
-
JQAD1
JQAD1 is a potent and selective histone acetyltransferase EP300 degrader (PROTAC?; DC50≤ 31.6 nM); comprises an EP300 inhibitor, A485, joined by a linker to a cereblon E3 ligase ligand.
