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PROSTAGLANDIN A1

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Products Intro: Product Name:PROSTAGLANDIN A1
CAS:14152-28-4
Purity:99% Package:1KG;1USD
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Products Intro: Product Name:Prostaglandin A1
CAS:14152-28-4
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Products Intro: Product Name:PROSTAGLANDIN A1
CAS:14152-28-4
Purity:99% Package:1KG;25kg;200kg;1000kg Jessica Remarks:g-kg-tons,free sample is available.Bottle/drum/IBC.Advantage products,new batches,regular stock, ready for shipment.
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Products Intro: Product Name:Prostaglandin A1
CAS:14152-28-4
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Company Name: SHANGHAI KEAN TECHNOLOGY CO., LTD.
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Products Intro: Product Name:4-Bromophenylacetone
CAS:14152-28-4
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PROSTAGLANDIN A1 manufacturers

  • Prostagladin E1
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  • $0.00 / 25Kg/Bag
  • 2025-11-19
  • CAS:14152-28-4
  • Min. Order: 2Kg/Bag
  • Purity: 99% up, High Density
  • Supply Ability: 20 tons
  • PROSTAGLANDIN A1
  • PROSTAGLANDIN A1 pictures
  • $1.00 / 1KG
  • 2020-02-20
  • CAS:14152-28-4
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 200kgs
PROSTAGLANDIN A1 Basic information
Product Name:PROSTAGLANDIN A1
Synonyms:prostaglandina(sup1);prostaglandine(sup1)-217;prostaglandina1syntheticcrystalline;(13E,15S)-15-Hydroxy-9-oxoprosta-10,13-dien-1-oic acid, PGA1;(13E)-(15S)-15-Hydroxy-9-oxoprosta-10,13-dienoate;C04685;ProstaglandinA1,(13E,15S)-15-Hydroxy-9-oxoprosta-10,13-dien-1-oic acid, PGA1;Prostaglandin A1 (25 mg)
CAS:14152-28-4
MF:C20H32O4
MW:336.47
EINECS:682-017-9
Product Categories:
Mol File:14152-28-4.mol
PROSTAGLANDIN A1 Structure
PROSTAGLANDIN A1 Chemical Properties
Melting point 43°C
Boiling point 392.93°C (rough estimate)
density 1.0192 (rough estimate)
refractive index 1.4434 (estimate)
storage temp. -20°C
solubility acetone: 10 mg/mL, clear
form White solid.
pka4.77±0.10(Predicted)
color Off-white
biological sourcesynthetic
BRN 2003401
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
Safety Information
Safety Statements 22-24/25
WGK Germany 3
RTECS GY5977900
8-10
HS Code 2937500000
MSDS Information
ProviderLanguage
SigmaAldrich English
PROSTAGLANDIN A1 Usage And Synthesis
DescriptionProstaglandin A1 (PGA1) was first isolated as a dehydration product of the PGE1 compounds found in human semen. It has been shown to cause renal vasodilation, increased urine sodium excretion, and lowered arterial pressure in hypertensive patients. It also has growth-inhibitory activity on tumor cells; the IC50 value for the inhibition of human ovarian cancer is 7.5 μM.
UsesProstaglandin A1 has been shown to inhibit human immunodeficiency virus type 1 (HIV-1) replication in various cell types. In addition, as a precursor to the anti-inflammatory prostaglandins, it activates pro-inflammatory PGD2 receptor CRTH2 initiating the anti-inflammatory response.
DefinitionChEBI: Prostaglandin A1 is a prostaglandins A. It is a conjugate acid of a prostaglandin A1(1-).
General DescriptionProstaglandin A1(PGA1) belongs to the class of cyclopentenone prostaglandin. PGA1 is generated by the dehydration of prostaglandin E1 (PGE1).
Biochem/physiol ActionsProstaglandin A1 (PGA1) boosts the expression of human liver-specific cytochrome P450 4F3B (CYP4F3B) and stimulates the synthesis of 20-hydroxy-eicosatetraenoic acids (HETEs). It has an ability to stimulate cell differentiation, ferritin synthesis and heat shock response in human cells. PGA1 exhibits antitumor and antiviral activities. In addition, it also elicits anti-inflammatory effects by activating peroxisome proliferator-activated receptor (PPAR). Elevated levels of PGA1 has been observed in hypertension patients.
Enzyme inhibitorThis eicosanoid (FWfree-acid = 336.47 g/mol; CAS 14152-28-4; Symbol: PGA1) induces apoptosis and stimulates the expression of stress genes. The structure and role of the prostaglandin A1 was investigated by Bergstr?m and Samuelsson, who shared the 1982 Nobel Prize in Physiology or Medicine for their pioneering work on the eicosanoids. Target(s): CYP4F2; DNA topoisomerase II; HIV-1 transcription; 3ahydroxysteroid dehydrogenase, NADP+-dependent; IkB kinase; Mayaro virus replication; stress-induced NF-kB activation; and virus protein biosynthesis, or translation.
References[1] SANDRA J. LEE . Renal effects of prostaglandin A1 in patients with essential hypertension[J]. Kidney international, 1972, 1 4: Pages 254-262. DOI:10.1038/ki.1972.35
[2] MOKHTAR K. TOPPOZADA MD. Treatment of preeclampsia with prostaglandin A1[J]. American journal of obstetrics and gynecology, 1988, 159 1: Pages 160-165. DOI:10.1016/0002-9378(88)90514-5
[3] ANTONIO ROSSI. Anti-inflammatory cyclopentenone prostaglandins are direct inhibitors of IκB kinase[J]. Nature, 2000, 403 6765: 103-108. DOI:10.1038/47520
[4] ASIM K MANDAL. Yin-yang: balancing act of prostaglandins with opposing functions to regulate inflammation.[J]. Journal of immunology, 2005, 175 10: 6271-6273. DOI:10.4049/jimmunol.175.10.6271
[5] STEFANIA CARTA . Prostaglandin A1 inhibits avian influenza virus replication at a postentry level: Effect on virus protein synthesis and NF-κB activity[J]. Prostaglandins, leukotrienes, and essential fatty acids, 2014, 91 6: Pages 311-323. DOI:10.1016/j.plefa.2014.07.009
[6] ATSUKO TSUKIMOTO . A new role for PGA1 in inhibiting hepatitis C virus-IRES-mediated translation by targeting viral translation factors[J]. Antiviral research, 2015, 117: Pages 1-9. DOI:10.1016/j.antiviral.2015.01.013
[7] BEATRIZ DÍEZ-DACAL. Identification of aldo-keto reductase AKR1B10 as a selective target for modification and inhibition by prostaglandin A(1): implications for antitumoral activity.[J]. Cancer research, 2011: 4161-4171. DOI:10.1158/0008-5472.can-10-3816
[8] B ANTA. PGA1-induced apoptosis involves specific activation of H-Ras and N-Ras in cellular endomembranes[J]. Cell Death & Disease, 2016, 7 7: e2311-e2311. DOI:10.1038/cddis.2016.219
PROSTAGLANDIN A1 Preparation Products And Raw materials
Tag:PROSTAGLANDIN A1(14152-28-4) Related Product Information
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