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Phorbol 12,13-dibutyrate
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Phorbol 12,13-dibutyrate图片
CAS NO:37558-16-0
包装:1mg
市场价:1008元

化学性质

Physical AppearanceWhite lyophilised solid
StorageStore at -20°C
M.Wt504.61
Cas No.37558-16-0
FormulaC28H40O8
Solubility<25.23mg/ml in DMSO
Chemical Name(1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-1a,1b,4,4a,5,7a,7b,8,9,9a-decahydro-1H-cyclopropa[3,4]benzo[1,2-e]azulene-9,9a-diyl dibutyrate
Canonical SMILESO[C@@]1([C@H](C=C(C)C2=O)[C@]32O)[C@@H](C=C(CO)C3)[C@H](C4(C)C)[C@]4([C@@H]([C@H]1C)OC(CCC)=O)OC(CCC)=O
运输条件蓝冰运输或根据您的需求运输。
一般建议为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。

资料参考

Phorbol 12,13-dibutyrate, a phorbol ester, is an activator of PKC, including the conventional calcium-dependent subtypes (α and γ), the nonconventional calcium-independent isoforms (δ, ε, η), as well as the atypical calcium-independent and DAG or phorbol ester-unresponsive subtype (ζ). PKC plays an important role in the regulation of a variety of cellular processes such as exocytosis, gene expression, cell proliferation and differentiation, as well as tumor promotion, thereby representing the major target for tumor-promoting phorbol esters and chemically unrelated tumor promoters. Phorbol esters are able to replace the endogenous activator DAG in the stimulation of PKC, and participate in the multistage process of tumor formation and progression.

References:

1. Geiges D, Meyer T, Marte B, et al. Activation of protein kinase C subtypes alpha, gamma, delta, epsilon, zeta, and eta by tumor-promoting and nontumor-promoting agents. Biochemical Pharmacology, 1997, 53(6): 865-875.

2. Middleton JP, Khan WA, Collinsworth G, et al. Heterogeneity of protein kinase C-mediated rapid regulation of Na/K-ATPase in kidney epithelial cells. Journal of Biological Chemistry, 1993, 268(21): 15958-15964.

3. Scribner JD, Boutwell RK. Inflammation and tumor promotion: selective protein induction in mouse skin by tumor promoters. European Journal of Cancer, 1972, 8(6): 617-621.

试验操作

Cell experiment:[2]

Cell lines

OK and LLC-PK1cells expressing detectable levels of PKCα and PKCζ

Reaction Conditions

1 mM phorbol 12,13-dibutyrate for 10 min incubation

Applications

Phorbol 12,13-dibutyrate activated PKC, and inhibited Na/K-ATPase transport activity in OK cells, but not in LLC-PK1cells.

Animal experiment:[3]

Animal models

Female CD-1 mice, 8 weeks of age

Dosage form

Female CD-1 mice, 8 weeks of age

Topical administration

Applications

Phorbol 12,13-dibutyrate induced papilloma formation in mice with a total dose of 9.7 μmol required to produce papillomas in 50% of survivors after eight weeks. Phorbol 12,13-dibutyrate also induced inflammation in 50% of mice when administered topically to the ear at a dose of 0.067 μmol/ear.

Note

The technical data provided above is for reference only.

References:

1. Geiges D, Meyer T, Marte B, et al. Activation of protein kinase C subtypes alpha, gamma, delta, epsilon, zeta, and eta by tumor-promoting and nontumor-promoting agents. Biochemical Pharmacology, 1997, 53(6): 865-875.

2. Middleton JP, Khan WA, Collinsworth G, et al. Heterogeneity of protein kinase C-mediated rapid regulation of Na/K-ATPase in kidney epithelial cells. Journal of Biological Chemistry, 1993, 268(21): 15958-15964.

3. Scribner JD, Boutwell RK. Inflammation and tumor promotion: selective protein induction in mouse skin by tumor promoters. European Journal of Cancer, 1972, 8(6): 617-621.

 
 
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