Date published: 2026-5-18

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Prostaglandin G1 (CAS 52162-11-5)

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CAS Number:
52162-11-5
Molecular Weight:
370.48
Molecular Formula:
C20H34O6
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Prostaglandin G1, a derivative of prostaglandins, is a vital molecule in scientific research, primarily in the field of lipid biochemistry and cellular signaling pathways. Its mechanism of action revolves around its role as a lipid mediator, exerting diverse biological effects by binding to specific G protein-coupled receptors and activating downstream signaling cascades. In research, Prostaglandin G1 is utilized to investigate the physiological and pathological roles of prostaglandins in various cellular processes, including inflammation, immune responses, and vascular function. Moreover, Prostaglandin G1 serves as a valuable tool in elucidating the mechanisms underlying prostaglandin signaling, such as receptor-ligand interactions, intracellular signaling pathways, and downstream effector responses. Researchers also employ Prostaglandin G1 in studies focusing on drug discovery and development, where it is utilized to screen for novel compounds targeting prostaglandin receptors or modulating prostaglandin-mediated signaling pathways. Its versatile applications in lipid research and cellular signaling contribute to advancing our understanding of prostaglandin biology and its implications for various physiological and pathological conditions.


Prostaglandin G1 (CAS 52162-11-5) References

  1. Prostaglandin hydroperoxidase, an integral part of prostaglandin endoperoxide synthetase from bovine vesicular gland microsomes.  |  Ohki, S., et al. 1979. J Biol Chem. 254: 829-36. PMID: 104998
  2. A lipoxygenase from red alga Pyropia haitanensis, a unique enzyme catalyzing the free radical reactions of polyunsaturated fatty acids with triple ethylenic bonds.  |  Zhu, Z., et al. 2015. PLoS One. 10: e0117351. PMID: 25658744
  3. Non-peptide-based new class of platelet aggregation inhibitors: Design, synthesis, bioevaluation, SAR, and in silico studies.  |  Jaiswal, PK., et al. 2018. Arch Pharm (Weinheim). 351: e1700349. PMID: 29522645
  4. Analyzing the Therapeutic Mechanism of Mongolian Medicine Zhonglun-5 in Rheumatoid Arthritis Using a Bagging Algorithm with Serum Metabonomics.  |  Wang, X., et al. 2022. Evid Based Complement Alternat Med. 2022: 5997562. PMID: 36532854
  5. Peroxidase-dependent deactivation of prostacyclin synthetase.  |  Ham, EA., et al. 1979. J Biol Chem. 254: 2191-4. PMID: 372178
  6. Inhibition of prostaglandin endoperoxide synthetase by thiol analogues of prostaglandin.  |  Ohki, S., et al. 1977. Proc Natl Acad Sci U S A. 74: 144-8. PMID: 402003
  7. Dihomogammalinolenic acid, but not eicosapentaenoic acid, activates washed human platelets.  |  Siess, W., et al. 1984. Biochim Biophys Acta. 801: 265-76. PMID: 6089912
  8. Purification of prostaglandin endoperoxide synthetase from bovine vesicular gland microsomes.  |  Miyamoto, T., et al. 1976. J Biol Chem. 251: 2629-36. PMID: 816795
  9. Prostaglandin endoperoxide synthetase from bovine vesicular gland microsomes. Inactivation and activation by heme and other metalloporphyrins.  |  Ogino, N., et al. 1978. J Biol Chem. 253: 5061-8. PMID: 97287

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Prostaglandin G1, 500 µg

sc-215756
500 µg
$849.00