| Weight | 616.836 g/mol |
|---|---|
| Formula | C36H56O8 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 15 |
Phorbol 12-myristate 13-acetate (16561-29-8, 62-38-4)
Score:
#4 in Molecular and cellular biology
,
#203 in Biochemistry
,
#822 in Biology
,
#909 in Chemistry
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- Sigma-Aldrich - Phorbol 12-myristate 13-acetate84.00 - 870.00 USD
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- Amphiregulin: a bifunctional growth-modulating glycoprotein produced by the phorbol 12-myristate 13-acetate-treated human breast adenocarcinoma cell line MCF-7 (Proceedings of the National Academy of Sciences of the United States of America, 1988)
- Characterization of a promonocyte clone chronically infected with HIV and inducible by 13-phorbol-12-myristate acetate (Journal of Immunology, 1988)
- PKC-dependent Activation of Sphingosine Kinase 1 and Translocation to the Plasma Membrane EXTRACELLULAR RELEASE OF SPHINGOSINE-1-PHOSPHATE INDUCED BY PHORBOL 12-MYRISTATE 13-ACETATE (PMA) (Journal of Biological Chemistry, 2002)
- Fate of immunoprecipitable protein kinase C in GH3 cells treated with phorbol 12-myristate 13-acetate. (Journal of Biological Chemistry, 1985)
- Equalizing cDNA subtraction based on selective suppression of polymerase chain reaction: cloning of Jurkat cell transcripts induced by phytohemaglutinin and phorbol 12-myristate 13-acetate. (Analytical Biochemistry, 1996)
- A requirement for extracellular signal-regulated kinase (ERK) function in the activation of AP-1 by Ha-Ras, phorbol 12-myristate 13-acetate, and serum (Proceedings of the National Academy of Sciences of the United States of America, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCCCCCCCCCCC(=O)OC1C(C2(C(C=C(CC3(C2C=C(C3=O)C)O)CO)C4C1(C4(C)C)OC(=O)C)O)C
-
InChIKeyPHEDXBVPIONUQT-UHFFFAOYSA-N
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