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Merck

D3658

Sigma-Aldrich

1,9-Dideoxyforskolin from Coleus forskohlii

≥97%, solid

Sinónimos:

7β-Acetoxy-6β-hydroxy-8,13-epoxy-labd-14-en-11-one

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1 MG
MXP 2,400.00
5 MG
MXP 8,368.00

MXP 2,400.00


Fecha estimada de envío28 de mayo de 2025


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1 MG
MXP 2,400.00
5 MG
MXP 8,368.00

About This Item

Fórmula empírica (notación de Hill):
C22H34O5
Número de CAS:
Peso molecular:
378.50
Número MDL:
Código UNSPSC:
41106305
ID de la sustancia en PubChem:
NACRES:
NA.77

MXP 2,400.00


Fecha estimada de envío28 de mayo de 2025


Solicitar un pedido a granel

Ensayo

≥97%

Formulario

solid

actividad óptica

[α]26/D +93.6°, c = 6.12 in chloroform(lit.)

color

white to off-white

solubilidad

methanol: 28 mg/mL(lit.)
DMSO: 3 mg/mL(lit.)
chloroform: 50 mg/mL
ethanol: 6.6 mg/mL(lit.)
dilute aqueous acid and base: insoluble(lit.)

temp. de almacenamiento

−20°C

cadena SMILES

[H][C@@]12[C@H](O)[C@H](OC(C)=O)[C@@]3(C)O[C@](C)(CC(=O)C3[C@@]1(C)CCCC2(C)C)C=C

InChI

1S/C22H34O5/c1-8-20(5)12-14(24)16-21(6)11-9-10-19(3,4)17(21)15(25)18(26-13(2)23)22(16,7)27-20/h8,15-18,25H,1,9-12H2,2-7H3/t15-,16?,17-,18-,20-,21+,22-/m0/s1

Clave InChI

ZKZMDXUDDJYAIB-OJPJTMFRSA-N

Categorías relacionadas

Aplicación

Useful as a negative control for forskolin.

Acciones bioquímicas o fisiológicas

Biologically inactive forskolin analog. Does not stimulate adenylyl cyclase.

Características y beneficios

This compound is a featured product for Cyclic Nucleotide research. Click here to discover more featured Cyclic Nucleotide products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the Adenylyl cyclases page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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F Espinosa et al.
Developmental genetics, 25(2), 103-114 (1999-08-10)
The direct electrophysiological characterization of sperm Ca(2+) channels has been precluded by their small size and flat shape. An alternative to study these channels is to use spermatogenic cells, the progenitors of sperm, which are larger and easier to patch-clamp.
M Morales-Mulia et al.
Biochimica et biophysica acta, 1496(2-3), 252-260 (2000-04-20)
The role of the phospholemman (PLM) on the efflux of taurine and chloride induced by swelling was studied in HEK293 cells overexpressing stable transfected PLM. PLM, a substrate for protein kinases C and A, is a protein that induces an
V Brès et al.
British journal of pharmacology, 130(8), 1976-1982 (2000-08-22)
To characterize the volume-sensitive, osmolyte permeable anion channels responsible for the osmodependent release of taurine from supraoptic nucleus (SON) astrocytes, we investigated the pharmacological properties of the [(3)H]-taurine efflux from acutely isolated SON. Taurine release induced by hypotonic stimulus (250
Jatinder Ahluwalia
Biochemical and biophysical research communications, 375(4), 596-601 (2008-08-30)
Effective functioning of neutrophils relies upon electron translocation through the NADPH oxidase (NOX). The electron current generated (I(e)) by the neutrophil NADPH oxidase is electrogenic and rapidly depolarises the membrane potential in activated human neutrophils. Swelling activated chloride channels have
Atik Ure et al.
Neuroscience letters, 392(1-2), 10-15 (2005-09-21)
Effects of cAMP-activated protein kinases (PKA) on epileptic activity are at present studied in a model nervous system. Identified neurons in the buccal ganglia of the snail Helix pomatia were recorded with intracellular microelectrodes in a continuously perfused experimental chamber.

Artículos

Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.

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