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
Get Quotation Bulk Inquiry Add to Cart

Biological Information

  • Product Name
    2-methyl-2,3,4,5-tetrahydro-1,5-benzothiazepin-4-one
  • Note
    Research use only, not for human use.
  • Brief Description
    2-methyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is ligand of CBP.
  • Description
    2-methyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is ligand of CBP.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Chromatin/Epigenetic
  • Target
    Epigenetic Reader Domain
  • Recptor
    Human Endogenous Metabolite|GPR109B|AhR
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    96680-77-2
  • Formula Weight
    193.26
  • Molecular Formula
    C10H11NOS
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CC1CC(=O)Nc2ccccc2S1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With 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.
Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog
related products

  • SMARCA-BD ligand 1 f...

    SMARCA-BD ligand 1 for Protac dihydrochloride binds to the BAF ATPase subunit SMARCA2 and is used for degrading SMARCA2 based on PROTAC.

  • BRD4-BD1-IN-2

    BRD4-BD1-IN-2 is a selective and potent BRD4-BD1 inhibitor with an IC50 value of 2.51 μM, exhibiting 20-fold greater inhibitory activity against BRD4-BD1 compared to BRD4-BD2.

  • ODM-207

    BET-IN-4 is a potent BRD4 inhibitor.

Sign In Join Free