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비신돌릴말레이미드 I 염산염메이커 CAS 레지스트리 번호176504-36-2공급업체 | LookChem

비신돌릴말레이미드 I 염산염

기본 정보 Edit
  • 표준명:비신돌릴말레이미드 I 염산염
  • CAS 레지스트리 번호:176504-36-2
  • 분자식:C25H24N4O2.HCl
  • 분자 무게:0
  • HS 코드:2933998090
  • Mol 파일:176504-36-2.mol
비신돌릴말레이미드 I 염산염

동의어: 3-[1-(디메틸아미노프로필)인돌-3-일]-4-(인돌-3-일)말레이미드 염산염; 비신돌릴말레이미드 I(염산염); 비신돌릴말레이미드 I. 염산염 [GF-109203K;3-[1-[3-(디메틸아미노)프로필]-1H-인돌-3-일]-4-(1H-인돌-3-일)-1H-피롤-2,5-디온 일염산염;BIM 1염산염

관련 CAS 번호: 176851-48-2 13820-56-9 107807-24-9 177358-43-9 1185304-14-6 114113-11-0 104575-40-8 1633-09-6 134923-06-1 13507-80-7

표준명의 마케팅 및 가격
제조업체 및 유통업체:
  • 제조/브랜드
  • 화학물질 및 원자재
  • 포장
  • 가격
  • Sigma-Aldrich
  • GF 109203X hydrochloride ≥95%
  • 1mg
  • $ 178.00
  • Sigma-Aldrich
  • GF 109203X hydrochloride ≥95%
  • 250 μg
  • $ 67.60
  • Sigma-Aldrich
  • GF 109203X hydrochloride ≥95%
  • 250ug
  • $ 65.20
  • Sigma-Aldrich
  • Bisindolylmaleimide I, Hydrochloride An enhanced water-soluble form of Bisindolylmaleimide I.
  • 250ug
  • $ 65.20
  • Sigma-Aldrich
  • Bisindolylmaleimide I, Hydrochloride - CAS 176504-36-2 - Calbiochem An enhanced water-soluble form of Bisindolylmaleimide I.
  • 250 μg
  • $ 53.46
  • Sigma-Aldrich
  • Bisindolylmaleimide I, Hydrochloride An enhanced water-soluble form of Bisindolylmaleimide I.
  • 1mg
  • $ 140.60
  • Cayman Chemical
  • Bisindolylmaleimide I (hydrochloride) ≥98%
  • 5mg
  • $ 129.00
  • Cayman Chemical
  • Bisindolylmaleimide I (hydrochloride) ≥98%
  • 1mg
  • $ 40.00
  • Cayman Chemical
  • Bisindolylmaleimide I (hydrochloride) ≥98%
  • 500μg
  • $ 25.00
  • American Custom Chemicals Corporation
  • BISINDOLYLMALEIMIDE I HYDROCHLORIDE 95.00%
  • 5MG
  • $ 986.15
총 9 개 원재료 공급업체
표준명의 화학적 성질 Edit
물리적 데이터:
안전정보:
  • 픽토그램:
  • 위험 코드:
  • 진술:
  • 안전 선언문:
사용:
  • 소개 및 적용: GF 109203X hydrochloride, also known as Bisindolylmaleimide I (BIM I), is a highly selective and cell-permeable inhibitor of protein kinase C (PKC) with a Ki value of 14 nM. It is structurally similar to staurosporine, but shows higher selectivity for PKCα, β1, β2, γ, δ, and ε isozymes. BIM I acts as a competitive inhibitor for the ATP binding site of PKC and also inhibits glycogen synthase kinase-3 (GSK-3) with an IC50 value of 360 nM in primary adipocyte lysates and 170 nM in GSK3β immunoprecipitates derived from rat epididymal adipocytes. In addition, BIM I prevents collagen-triggered adenosine and ATP secretion and inhibits collagen and α-thrombin-induced platelet aggregation. It also functions as an anti-inflammatory agent and competitively antagonizes the serotonin (5-HT) receptor subtype 5-HT3 with a Ki value of 61 nM.
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