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  3. BET BD2-IN-1

BET BD2-IN-1 (compound 45) is a potent and selective inhibitor of BET BD2 (IC50=1.6 nM). BET BD2-IN-1 inhibits the differentiation of Th17 cells by decreasing the activation of STAT3 and NF-κB. BET BD2-IN-1 is used in psoriasis and inflammatory bowel disease (IBD) research.

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BET BD2-IN-1

BET BD2-IN-1 Estructura química

No. CAS : 2677039-24-4

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Descripciòn

BET BD2-IN-1 (compound 45) is a potent and selective inhibitor of BET BD2 (IC50=1.6 nM). BET BD2-IN-1 inhibits the differentiation of Th17 cells by decreasing the activation of STAT3 and NF-κB. BET BD2-IN-1 is used in psoriasis and inflammatory bowel disease (IBD) research[1].

IC50 & Target

BRD2 BD1

570 nM (IC50)

BRD2 BD2

5.9 nM (IC50)

BRD3 BD1

465 nM (IC50)

BRD3 BD2

6.0 mM (IC50)

BRD4 BD1

524 nM (IC50)

BRD4 BD2

1.6 nM (IC50)

BRDT BD1

527 nM (IC50)

In Vitro

BET BD2-IN-1 (500 nM) effectively inhibits Th17 cell differentiation and has excellent selectivity for BD2 over BD1[1].
BET BD2-IN-1 (4 nM) binds to BRD4 BD2 in intact cells and has stabilization effect on BRD4 BD2[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Differentiation Assay[1]

Cell Line: Th17 cells
Concentration: 500 nM
Incubation Time:
Result: Showed the strongest inhibitory activity and reduced differentiation from 19.0 to 7.81%.

Cell Migration Assay [1]

Cell Line: HEK 293 T cells
Concentration: 4, 20, 100, 500, 2500, 10000 nM
Incubation Time: 30 min
Result: Stabilized BRD4 BD2 at 50.4 °C.
In Vivo

BET BD2-IN-1 (20 mg/kg for i.v; once daily for seven days) inhibits the protein expression of p-STAT3 and p-NF-κB in mouse skin tissues, effectively ameliorates the pathological changes in the psoriasis mouse model[1].
BET BD2-IN-1 (20 mg/kg for i.v; once daily for seven days) significantly decreases the disease activity index (DAI) score in dextran sulfate sodium (DSS) induced IBD mouse model[1].
Pharmacokinetic Analysis of BET BD2-IN-1 in Sprague Dawley Rats Model[1]

parameter AUC(0‑t) (ng•h/mL) C0 (ng/mL) T1/2 (h) CL (mL/kg/min) Vdss (L/kg)
iv(1 mg/kg) 272 ± 7.2 279 ± 78 1.5 ± 0.1 60 ± 2.0 6.6 ± 0.8
parameter AUC(0‑t) (ng•h/mL) Cmax (ng/mL) T1/2 (h) Tmax (h) F (%)
po(10 mg/kg) 78 ± 34 20 ± 11 1.9 ± 0.2 2.7 ± 1.2 2.9 ± 1.2

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Imiquimod (HY-B0180)-induced Psoriasis mouse model[1]
Dosage: 10 and 20 mg/kg
Administration: Intravenous injection (i.v.) ; Once daily for seven days
Result: Significantly alleviated the Imiquimod-induced skin lesions in a dose-dependent manner.
Obviously reduced the enlarged spleen.
Significantly decreased the expression of p-STAT3 and p-NF-κB in mouse skin tissues.
Animal Model: DSS (HY-116282C)-induced IBD mouse model[1]
Dosage: 10 and 20 mg/kg
Administration: Intravenous injection (i.v.) ; Once daily for seven days
Result: Effectively prevented colon shortening.
Effectively alleviated the DSS-induced weight loss.
Significantly alleviated the infiltration of inflammatory cells, areas of ulceration as well as loss of mucosal epithelium, and goblet cells caused by DSS.
Peso molecular

478.58

Fòrmula

C30H30N4O2

No. CAS

2677039-24-4

SMILES

O=C(C1=CC=CC(CN2C3=C(C=C4C5=C2C=CC=C5C(N4C)=O)C=CC=C3)=C1)NC6CCN(CC6)C

Envío

Room temperature in continental US; may vary elsewhere.

Almacenamiento

Please store the product under the recommended conditions in the Certificate of Analysis.

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Referencias
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Inquiry Information

Nombre del producto:
BET BD2-IN-1
Cat. No.:
HY-155680
Cantidad:
MCE Japan Authorized Agent: