A-205804 化学構造
分子量: 300.4


Quality Control & MSDS


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製品説明 A-205804 is a potent and selective inhibitor of E-selectin and ICAM-1 expression with IC50 of 20 nM and 25 nM respectively.
ターゲット E-selectin ICAM-1
IC50 20 nM 25 nM [1]
In vitro試験 A-205804 selectively inhibits the surface expression of the cell adhesion molecules ICAM-1 and E-selectin in human endothelial cells. A-205804 inhibites the IL-1β-induced expression of E-selectin (IC50 = 20 nM) and ICAM-1 (IC50 = 10 nM) with essentially the same level of potency as that for TNFα-induced expression. For reasons which are unclear, the ability of A-205804 to inhibit PMA-induced E-selectin expression is significantly reduced (IC50 > 1000 nM), but A-205804 is a potent inhibitor of ICAM-1 expression (IC50 = 40 nM) using this protein-kinase C-activating agent. [2]
In vivo試験

プロトコル (参考用のみ)

キナーゼアッセイ: [1]

Cell ELISA Assay Primary HUVECs are plated in 96-well plates at 5 × 104 cells/mL in EBM/2% FBS/human epidermal growth factor/bovine brain extract/gentamicin. The following day test compounds are added and the plates incubats for 24 h at 37 °C. TNFα then is added to a final concentration of 5 ng/mL, and the plates are incubated for an additional 6 h at 37 °C. The plates are washed once with D-PBS, and primary antibody is added in D-PBS/2% BSA /0.01% NaN3. The antibodies used are mouse monoclonal anti-ELAM-1, anti-ICAM-1, and anti-VCAM-1. The plates are stored overnight at 4 °C and then washes three times with D-PBS. Secondary antibody, HRP-conjugated donkey anti-mouse IgG in D-PBS/2%BSA, is added, and the plates are incubated for 1−2 h at room temperature and then washes three times with D-PBS. OPD solution is added to the wells, the plates are developed for 15−20 min and neutralizes with 1 N sulfuric acid, and the absorbance is read at 490 nm.

Conversion of different model animals based on BSA (Value based on data from FDA Draft Guidelines)

SpeciesMouseRatRabbitGuinea pigHamsterDogMonkeyBaboon
Weight (kg)
Body Surface Area (m2)0.0070.0250.
Km factor361285201220
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for resveratrol of 11.2 mg/kg.

Rat dose (mg/kg) = mouse dose (22.4 mg/kg) ×  mouse Km(3)  = 11.2 mg/kg
rat Km(6)



Download A-205804 SDF
分子量 300.4


CAS No. 251992-66-2
保管 2年-20℃
6月-80℃in solvent
別名 N/A
溶解度 (25°C) * In vitro DMSO 60 mg/mL (199.73 mM)
<1 mg/mL (<1 mM)
エタノール <1 mg/mL (<1 mM)
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
化学名 Thieno[2,3-c]pyridine-2-carboxamide, 4-[(4-methylphenyl)thio]-



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Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID