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37558-16-0

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  • Butanoic acid,(1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-1,1a,1b,4,4a,5,7a,7b,8,9-decahydro-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-9aH-cyclopropa[3,4]benz[1,2-e]azulene-9,9a-diylester

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  • Shandong Hanjiang Chemical Co., Ltd.
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  • Butanoic acid,(1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-1,1a,1b,4,4a,5,7a,7b,8,9-decahydro-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-9aH-cyclopropa[3,4]benz[1,2-e]azulene-9,9a-diylester

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  • Henan Wentao Chemical Product Co., Ltd.
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  • Butanoic acid,(1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-1,1a,1b,4,4a,5,7a,7b,8,9-decahydro-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-9aH-cyclopropa[3,4]benz[1,2-e]azulene-9,9a-diylester

    Cas No: 37558-16-0

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  • Hangzhou J&H Chemical Co., Ltd.
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  • Butanoic acid,(1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-1,1a,1b,4,4a,5,7a,7b,8,9-decahydro-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-9aH-cyclopropa[3,4]benz[1,2-e]azulene-9,9a-diylester

    Cas No: 37558-16-0

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  • Henan Tianfu Chemical Co., Ltd.
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37558-16-0 Usage

Description

PHORBOL 12,13-DIBUTYRATE, also known as a phorbol ester, is a white solid compound that has been widely utilized in various research applications. It is known for its ability to activate protein kinase C (PKC), a critical enzyme involved in numerous cellular processes.

Uses

Used in Pharmaceutical Research:
PHORBOL 12,13-DIBUTYRATE is used as a PKC activator for studying its effects on human organic anion transporter 4 (hOAT4) activity. This application is crucial in understanding the role of PKC in the regulation of transporter proteins, which can have implications for drug development and treatment of various diseases.
Used in Cellular and Molecular Biology:
PHORBOL 12,13-DIBUTYRATE is used as a PKC activator to analyze its effects on galectin-3 expression and matrix production in HL-1 cells. This application aids in investigating the intricate relationships between PKC activation and cellular processes, such as cell adhesion, migration, and proliferation, which are essential for understanding various biological phenomena and potential therapeutic targets.

Reactivity Profile

PHORBOL 12,13-DIBUTYRATE may be sensitive to prolonged exposure to air, light and ambient temperatures. PHORBOL 12,13-DIBUTYRATE may also be subject to autooxidation.

Fire Hazard

The flash point of PHORBOL 12,13-DIBUTYRATE has not been determined, but PHORBOL 12,13-DIBUTYRATE is probably combustible.

Biological Activity

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.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.

Biochem/physiol Actions

Phorbol 12,13-dibutyrate (PDBu) is a potent activator of protein kinase C (PKC). It is more hydrophilic than phorbol 12-myristate 13-acetate (PMA), which facilitates washing PDBu out of cells in tissue culture. PDBu activates endothelial nitric oxide synthase expression in primary human umbilical vein endothelial cells, which in turn correlates with PKC α and ε expression.

Check Digit Verification of cas no

The CAS Registry Mumber 37558-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,5 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37558-16:
(7*3)+(6*7)+(5*5)+(4*5)+(3*8)+(2*1)+(1*6)=140
140 % 10 = 0
So 37558-16-0 is a valid CAS Registry Number.
InChI:InChI=1/C28H40O8/c1-7-9-20(30)35-24-16(4)27(34)18(22-25(5,6)28(22,24)36-21(31)10-8-2)12-17(14-29)13-26(33)19(27)11-15(3)23(26)32/h11-12,16,18-19,22,24,29,33-34H,7-10,13-14H2,1-6H3

37558-16-0 Well-known Company Product Price

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  • Sigma

  • (P1269)  Phorbol 12,13-dibutyrate  ≥98% (TLC), powder

  • 37558-16-0

  • P1269-1MG

  • 885.69CNY

  • Detail
  • Sigma

  • (P1269)  Phorbol 12,13-dibutyrate  ≥98% (TLC), powder

  • 37558-16-0

  • P1269-5MG

  • 2,508.48CNY

  • Detail
  • Sigma

  • (P1269)  Phorbol 12,13-dibutyrate  ≥98% (TLC), powder

  • 37558-16-0

  • P1269-10MG

  • 5,277.87CNY

  • Detail

37558-16-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name phorbol 12,13-dibutanoate

1.2 Other means of identification

Product number -
Other names PDBU

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:37558-16-0 SDS

37558-16-0Downstream Products

37558-16-0Relevant articles and documents

A new class of simplified phorbol ester analogues: Synthesis and binding to PKC and ηPKC-C1B (ηPKC-CRD2)

Wender, Paul A.,Kirschberg, Thorsten A.,Williams, Peter D.,Bastiaans, Harold M. M.,Irie, Kazuhiro

, p. 1009 - 1012 (1999)

(matrix presented) A unique class of simplified phorbol ester analogues is described for the first time. A highly efficient retro-annelation sequence was developed in order to remove the five-membered ring from the phorbol diterpene core, allowing access

Modulation of the transient receptor potential vanilloid channel TRPV4 by 4α-phorbol esters: A structure-activity study

Klausen, Thomas Kj?r,Pagani, Alberto,Minassi, Alberto,Ech-Chahad, Abdellah,Prenen, Jean,Owsianik, Grzegorz,Hoffmann, Else Kay,Pedersen, Stine Falsig,Appendino, Giovanni,Nilius, Bernd

experimental part, p. 2933 - 2939 (2010/03/03)

The mechanism of activation of the transient receptor potential vanilloid 4 (TRPV4) channel by 4α-phorbol esters was investigated by combining information from chemical modification of 4α-phorbol-didecanoate (4α-PDD, 2a), site-directed mutagenesis, Casup

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