GLPBio

SB273005

Catalog No.: GC14143Purity:>99.50%
SB273005 は、αvβ3 受容体と αvβ5 受容体の Kis がそれぞれ 1.2 nM と 0.3 nM の強力な非ペプチド性で経口的に活性なインテグリン アンタゴニストです。

製品は研究用途にのみ使用できます。人体には使用できません。患者への販売は行っておりません。


SB273005
Cas No.: 205678-31-5
10mM (in 1mL DMSO)In Stock
$154.00
1
5mgIn Stock
$140.00
1
10mgIn Stock
$243.00
1
25mgIn Stock
$513.00
1

引用文献 (Citations)

1 publications本製品を使用した研究者による文献

製品説明 (Description)

SB 273005 is a potent nonpeptide antagonist of αvβ3 (vitronectin receptor), with Ki values of 1.2 nM and 0.3 nM to two closely related integrins, αvβ3 and αvβ5, respectively [1].

αvβ3 belongs to the integrin family of adhesion molecules. It is a heterodimer. It mediates cell adhesion to serum proteins and extracellular matrix via the recognition of the arg-gly-asp (RGD) sequence [1].

SB 273005 binds αvβ3 and αvβ5 with low nM affinity, but binds weakly to integrins αIIbβ3 and α5β1. SB 273005 inhibits αvβ3-mediated cell adhesion with an IC50 value of 3 nM, endothelial cell migration with an IC50 of 1.8 nM, and osteoclast-mediated bone resorption with an IC50 of 11 nM in vitro [1].

The αvβ3 integrin is pivotal in bone resorption [2]. In the chronic ovx and thyroparathyroidectomized bone resorption rat models, SB 273005 as well as other similar vitronectin receptor antagonists, inhibit bone loss. In AIA rats, prophylactical treatment with SB 273005 at doses of 60, 30, and 10 mg/kg twice daily significantly normalized bone mineral density (BMD). Normalization values of BMD were 69%, 42%, and 44% for doses of 60, 30, and 10 mg/kg twice daily, respectively. A single daily dose of SB 273005 significantly improved BMD (24% normalization) only when SB 273005 was prophylactically administered at 60 mg/kg [1].

References:
[1].  Badger AM, Blake S, Kapadia R, et al. Disease-modifying activity of SB 273005, an orally active, nonpeptide αvβ3 (vitronectin receptor) antagonist, in rat adjuvant-induced arthritis. Arthritis & Rheumatism, 2001, 44(1): 128-137.
[2].  Murphy MG, Cerchio K, Stoch SA, et al. Effect of L-000845704, an αvβ3 integrin antagonist, on markers of bone turnover and bone mineral density in postmenopausal osteoporotic women. The Journal of Clinical Endocrinology & Metabolism, 2005, 90(4): 2022-2028.

実験プロトコル (Protocol)

Cell experiment [1]:

Cell lines

MDA-MB-231 breast adenocarcinoma cell

Preparation method

Soluble in DMSO. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.

Reacting condition

1 μmol/l

Applications

In blood containing MDA-MB-231 cells, a combination of SB273005 and lamifiban inhibited tumor cell adhesion to vascular extracellular matrix (ECM).

Animal experiment [2]:

Animal models

Male Lewis rats with adjuvant-induced arthritis

Dosage form

Oral administration, 10, 30, and 60 mg/kg, twice per day

Application

In rat with adjuvant-induced arthritis, SB273005 (30 mg/kg, 60 mg/kg, p.o.) significantly reduced the symptoms of adjuvant-induced arthritis. When administered prophylactically to AIA rats, SB 273005 (twice per day) inhibited paw edema at doses of 10, 30, and 60 mg/kg, by 40%, 50%, and 52%, respectively.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. Gomes N, Vassy J, Lebos C, et al. Breast adenocarcinoma cell adhesion to the vascular subendothelium in whole blood and under flow conditions: Effects of α v β 3 and α IIb β 3 antagonists[J]. Clinical and Experimental Metastasis, 2004, 21(6): 553-561. [2]. Badger A M, Blake S, Kapadia R, et al. Disease‐modifying activity of SB 273005, an orally active, nonpeptide αvβ3 (vitronectin receptor) antagonist, in rat adjuvant‐induced arthritis[J]. Arthritis & Rheumatology, 2001, 44(1): 128-137.

製品資料 (Product Documents)

Purity:>99.50%Appearance:A solid

化学的性質 (Chemical Properties)

CAS番号
205678-31-5
化学名
(S)-2-(8-(2-(6-(methylamino)pyridin-2-yl)ethoxy)-3-oxo-2-(2,2,2-trifluoroethyl)-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl)acetic acid
SMILES
CNC1=CC=CC(CCOC(C=C2CN3CC(F)(F)F)=CC=C2C[C@@](C3=O)([H])CC(O)=O)=N1
分子式
C22H24F3N3O4
分子量
451.44
溶解性
DMSO : 100 mg/mL (221.51 mM; Need ultrasonic)
保存条件
Store at -20°C
一般的な注意事項
製品の溶解性データに基づいて適切な溶媒を選択してください。調製後は、凍結融解の繰り返しを避けるため、ストック溶液を小分けしてください。
ストック溶液は、-80°Cで保存する場合は6か月以内、-20°Cで保存する場合は1か月以内に使用してください。
溶解性を高めるには、チューブを37°Cに温め、適切な時間超音波処理してください。
配送条件
評価用サンプルは保冷剤とともに発送します。その他の容量は室温で発送し、ご要望に応じて保冷剤を同梱します。

計算ツール (Calculators)モル濃度 / 希釈 / 分子量 / 単位変換 / in vivo製剤 / 溶解度

g/mol

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