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시클로 피아 존산메이커 CAS 레지스트리 번호18172-33-3공급업체 | LookChem

시클로 피아 존산

기본 정보 Edit
  • 표준명:시클로 피아 존산
  • CAS 레지스트리 번호:18172-33-3
  • 분자식:C20H20N2O3
  • 분자 무게:336.39
  • HS 코드:29337900
  • Mol 파일:18172-33-3.mol
시클로 피아 존산

동의어: (6a-alpha,11a,11b-alpha)–10-acetyl-7-dimethyl-11-hydroxy-;9h-pyrrolo(1’,2’:2,3)isoindolo(4,5,6-cd)indol-9-one,2,6,6a,7,11a,11b-hexahydro;(6AA, 10Z, 11AB, 11BA)-6A,7,11A,11B-TETRAHYDRO-10-(1-HYDROXYETHYLIDENE)-7,7- DIMETHYL-6H-PYRROLO [1′,2′:2,3]ISOINDOLO [4,5,6-CD]INDOLE-9,11 (2H,10H)-DIONE;(6AR,11AS,11BR)-REL-10-ACETYL-2,6,6A,7,11A,11B-HEXAHYDRO-7,7-DIMETHYL-9H-PYRROLO[1′,2′:2,3]ISOINDOLO[4,5,6-CD]INDOL-9-ONE;ALPHA CYCLOPIAZONIC ACID;CPA;CYCLOPIAZONIC ACID;CYCLOPIAZONIC ACID, PENICILLIUM CYCLOPIUM

관련 CAS 번호: 1261615-96-6 1289387-63-8 111011-00-8 19688-04-1 1245647-59-9 1020253-02-4 115722-26-4 125812-04-6 129526-60-9 101420-81-9

표준명의 마케팅 및 가격
제조업체 및 유통업체:
  • 제조/브랜드
  • 화학물질 및 원자재
  • 포장
  • 가격
  • TRC
  • Cyclopiazonic Acid,
  • 1mg
  • $ 45.00
  • Sigma-Aldrich
  • Cyclopiazonic acid from Penicillium cyclopium ≥98% (HPLC), powder
  • 5mg
  • $ 98.60
  • Sigma-Aldrich
  • Cyclopiazonic Acid, A cell-permeable, reversible inhibitor of sarcoplasmic reticulum Ca
  • 5mg
  • $ 74.92
  • Sigma-Aldrich
  • Cyclopiazonic acid from Penicillium cyclopium ≥98% (HPLC), powder
  • 10mg
  • $ 172.00
  • Sigma-Aldrich
  • Cyclopiazonic acid from Penicillium cyclopium ≥98% (HPLC), powder
  • 50mg
  • $ 619.00
  • ChemScene
  • Cyclopiazonic Acid, >99.0%
  • 10mg
  • $ 430.00
  • ChemScene
  • Cyclopiazonic Acid, >99.0%
  • 5mg
  • $ 250.00
  • Cayman Chemical
  • Cyclopiazonic Acid ≥95%
  • 5mg
  • $ 57.00
  • Cayman Chemical
  • Cyclopiazonic Acid ≥95%
  • 1mg
  • $ 19.00
  • Cayman Chemical
  • Cyclopiazonic Acid ≥95%
  • 10mg
  • $ 99.00
총 19 개 원재료 공급업체
표준명의 화학적 성질 Edit
물리적 데이터:
안전정보:
  • 픽토그램:
  • 위험 코드:
  • 진술: 25
  • 안전 선언문:
사용:
  • 소개 및 적용: Cyclopiazonic acid (CPA) is a mycotoxin produced by various Aspergillus and Penicillium species. It is a highly specific inhibitor of calcium ATPase of sarcoplasmic reticulum, which alters calcium homeostasis and ATP-dependent calcium transport, resulting in the release of intracellular stored Ca2+ without increasing IP3. CPA has been used in various applications, such as an anti-arrhythmic agent in Langendorff-perfused murine hearts, a decrease in hormone-sensitive lipase activity and triacylglycerol hydrolysis in rat soleus muscle, and an inhibitor of endoplasmic reticulum Ca2+-ATPase. It has also been used as a standard in aflatoxin detection and quantification, a component in Ca2+-free DMEM/10% fetal bovine serum, a reversible inhibitor of the sarco/endoplasmic reticulum Ca2+-ATPase (SERCA) to examine the role of luminal calcium in ER-to-Golgi trafficking, and an endoplasmic reticulum Ca2+-ATPase blocker to treat neurons and study the role of the ER in releasing and sustaining Ca2+ during Ca2+-induced Ca2+ release (CICR) to inhibit SERCA. In vivo, CPA can induce ptosis, hypothermia, tremor, and cachexia, as well as lethality in rats, and tachycardia and sedation in rabbits when administered at a dose of 10 mg/kg.
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