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Aflibercept (Synonyms: VEGF Trap; VEGF-TRAPR1R2; VEGF-trapR1)

Catalog No.GC68628

Aflibercept는 고친화성 솔러블 디코이 동맥 내피 성장 인자(VEGF) 수용체이고 강력한 혈관 생성 억제제로 동맥 내피 성장 인자와 태반 성장 인자(PlGF)를 경력한 혈관신생 억제제 결합할 수 있다. 전신적 연구는 Aflibercept가 흑색종과 고형 종양을 포함한 다양한 종양에 대해 강력한 항종양 및 항혈관 생성 활동을 보인다고 보여 준다.

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Aflibercept Chemical Structure

Cas No.: 862111-32-8

Size 가격 재고 수량
500ug
US$340.00
재고 있음
1mg
US$546.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description of Aflibercept

Aflibercept는 고친화성 솔러블 디코이 동맥 내피 성장 인자(VEGF) 수용체이고 강력한 혈관 생성 억제제로 동맥 내피 성장 인자와 태반 성장 인자(PlGF)를 경력한 혈관신생 억제제 결합할 수 있다. 전신적 연구는 Aflibercept가 흑색종과 고형 종양을 포함한 다양한 종양에 대해 강력한 항종양 및 항혈관 생성 활동을 보인다고 보여 준다.

Aflibercept (7.5μg/ml; 10분)는 갤렉틴-1에 의한 VEGFR2 활성을 억제한다[2]. Aflibercept (15nM; 1시간)는 ARPE-19와 HUVEC의 세포 표면 결합이 현저하지 않는다. Aflibercept (500nM; 10-15분)는 헹신의 존재하에 세로토닌의 방출을 자극할 수 없다[3].

Aflibercept (10mg/kg와 25mg/kg; SC; 매주 두 번; 30일)는 기초 종양 성장을 74%와 78%로 억제하고 검출 가능한 폐 전이 형성을 98%의 경우에 억제한다[4]. Aflibercept (10mg/kg; 3시간)는 중풍으로 인한 VEGF-A와 VEGFR2의 표현을 줄이고 뇌수종과 혈뇌 장벽의 파괴를 완화하고 중풍 후 중뇌동맥 폐색(MCAO) 후 비만 쥐의 생존율을 향상시킬 수 있다[5].

References:
[1] Bender J G, Blaney S M, Borinstein S, et al. A phase I trial and pharmacokinetic study of aflibercept (VEGF Trap) in children with refractory solid tumors: a children's oncology group phase I consortium report[J]. Clinical cancer research, 2012, 18(18): 5081-5089.
[2] Kanda A, Noda K, Saito W, Ishida S. Aflibercept Traps Galectin-1, an Angiogenic Factor Associated with Diabetic Retinopathy. Sci Rep. 2015 Dec 9;5:17946.
[3] MacDonald DA, Martin J, Muthusamy KK, Luo JK, Pyles E, Rafique A, Huang T, Potocky T, Liu Y, Cao J, Bono F, Delesque N, Savi P, Francis J, Amirkhosravi A, Meyer T, Romano C, Glinka M, Yancopoulos GD, Stahl N, Wiegand SJ, Papadopoulos N. Aflibercept exhibits VEGF binding stoichiometry distinct from bevacizumab and does not support formation of immune-like complexes. Angiogenesis. 2016 Jul;19(3):389-406.
[4] Moroney JW, Sood AK, Coleman RL. Aflibercept in epithelial ovarian carcinoma. Future Oncol. 2009 Jun;5(5):591-600.
[5] Kim ID, Cave JW, Cho S. Aflibercept, a VEGF (Vascular Endothelial Growth Factor)-Trap, Reduces Vascular Permeability and Stroke-Induced Brain Swelling in Obese Mice. Stroke. 2021 Aug;52(8):2637-2648.

Protocol of Aflibercept

세포 실험 [1]:

세포 라인

인간 RPE (hTERT-RPE1) 세포

제조 방법

인간 RPE (hTERT-RPE1) 세포는 Aflibercept (7.5μg/ml)로 10분 동안 처리되었습니다.

반응 조건

Aflibercept: 7.5μg/ml; 10분 동안

응용 분야

Aflibercept (7.5μg/ml; 10분)는 갤렉틴-1에 의한 VEGFR2 활성을 억제합니다.
동물 실험 [2]:

동물 모형

원위 쥐 신장암 세포 모델

제조 방법

Aflibercept 10mg/kg와 25mg/kg은 용매 대조군에 비해 매주 두 번 피하 주사로 최대 30일 동안 투여되었습니다.

제형

10 및 25mg/kg; SC; 매주 두 번; 30일 동안

응용 분야

Aflibercept (10mg/kg와 25mg/kg; SC; 매주 두 번; 30일)는 기초 종양 성장을 74%와 78%로 억제하고 검출 가능한 폐 전이 형성을 98%의 경우에 억제했습니다.

References:
[1] Kanda A, Noda K, Saito W, Ishida S. Aflibercept Traps Galectin-1, an Angiogenic Factor Associated with Diabetic Retinopathy. Sci Rep. 2015 Dec 9;5:17946.
[2] Moroney JW, Sood AK, Coleman RL. Aflibercept in epithelial ovarian carcinoma. Future Oncol. 2009 Jun;5(5):591-600.

Chemical Properties of Aflibercept

Cas No. 862111-32-8 SDF
Synonyms VEGF Trap; VEGF-TRAPR1R2; VEGF-trapR1
Formula M.Wt
Solubility Storage Sealed and stored at ≤ -30°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.
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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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리뷰

Review for Aflibercept

Average Rating: 5 ★★★★★ (Based on Reviews and 30 reference(s) in Google Scholar.)

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