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Merck
모든 사진(1)

문서

F3917

Sigma-Aldrich

Forskolin

For use in molecular biology applications

동의어(들):

7β-Acetoxy-8,13-epoxy-1α,6β,9α-trihydroxylabd-14-en-11-one, Coleonol, Colforsin

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About This Item

실험식(Hill 표기법):
C22H34O7
CAS Number:
Molecular Weight:
410.50
Beilstein:
1692716
EC Number:
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.52

생물학적 소스

Coleus forskohlii

설명

for activation of T cells

제품 라인

BioReagent

분석

≥98% (HPLC)

형태

powder

분자량

410.50  g/mol

색상

white to off-white

solubility

ethanol: soluble

적합성

suitable for inhibits interleukin 2 (IL-2) production in Jurkat cells

저장 온도

room temp

SMILES string

CC(=O)O[C@H]1[C@@H](O)[C@H]2C(C)(C)CC[C@H](O)[C@]2(C)[C@@]3(O)C(=O)C[C@@](C)(O[C@]13C)C=C

InChI

1S/C22H34O7/c1-8-19(5)11-14(25)22(27)20(6)13(24)9-10-18(3,4)16(20)15(26)17(28-12(2)23)21(22,7)29-19/h8,13,15-17,24,26-27H,1,9-11H2,2-7H3/t13-,15-,16-,17-,19-,20-,21+,22-/m0/s1

InChI key

OHCQJHSOBUTRHG-KGGHGJDLSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Forskolin is a cell permeable diterpenoid isolated from Coleus forskohlii.

생화학적/생리학적 작용

Cell-permeable diterpenoid that possesses anti-hypertensive, positive inotropic, and adenylyl cyclase activating properties. Many of its biological effects are due to its activation of adenylyl cyclase and the resulting increase in intracellular cAMP concentration. Forskolin effects calcium currents and inhibits MAP kinase.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Dermal

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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프로토콜

Learn how to cultivate similar-sized iPSC-derived colon organoids using Millicell® Microwell plates and perform a forskolin-induced swelling assay.

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