BCI-121

BCI-121
  • CAS No.:432529-82-3

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
Other grades of this product :
BCI-121 Basic information
Product Name:BCI-121
Synonyms:BCI-121;BCI 121;BCI121;BCI-121;1-{2-[(4-bromophenyl)amino]-2-oxoethyl}piperidine-4-carboxamide;1-Piperidineacetamide, 4-(aminocarbonyl)-N-(4-bromophenyl)-;BCL 121
CAS:432529-82-3
MF:C14H18BrN3O2
MW:340.22
EINECS:
Product Categories:
Mol File:432529-82-3.mol
BCI-121 Chemical Properties
storage temp. 2-8°C
form powder
color white to beige
Safety Information
HS Code 2933399990
MSDS Information
BCI-121 Usage And Synthesis
Biochem/physiol ActionsBCI-121 is a substrate-competitive SMYD3 inhibitor that reduces nuclear histone H3 lys4 di- and tri-methylation level (by 50%/H3K4me2 and 40%H3K4me3 in HT29 cells; 100 μM BCI-121 for 48 h), downregulates known SMYD3 target genes transcription, and selectively affects SMYD3-dependent proliferation of cancer cultures (46%/HT29 and 54%/HCT116 proliferation reduction; 100 μM BCI-121 for 72 h) with little antiproliferation efficacy toward low SMYD3-expressing cancer cells. BCI-121 targets SMYD3 via direct affinity interaction (kon 357.7/M/s; koff 4.23×10-3/s; KD=koff/kon = 11.8 μM) and effectively competes against histone for SMYD3 binding (%inhibition/[histone H4 peptide]:[BCI-121] ratio = 36.5%/1:1 and 51.0%/1:2.5).
BCI-121 Preparation Products And Raw materials

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