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PROSTAGLANDIN A1

CAS No.
14152-28-4
Chemical Name:
PROSTAGLANDIN A1
Synonyms
PGA1;Prostaglandin A;Prostagladin E1;C04685;pga(sub1);pga(sup1);Prostagladin A;PROSTAGLANDIN A1;PROSTAGLANDINS A1;prostaglandina(sup1)
CBNumber:
CB3666883
Molecular Formula:
C20H32O4
Molecular Weight:
336.47
MDL Number:
MFCD00077858
MOL File:
14152-28-4.mol
MSDS File:
SDS
Last updated:2023-06-08 09:01:57

PROSTAGLANDIN A1 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.
pka 4.77±0.10(Predicted)
color Off-white
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.
FDA UNII VYR271N44P

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Danger
Hazard statements  H302-H360F
Precautionary statements  P201-P301+P312+P330-P308+P313
Safety Statements  22-24/25
WGK Germany  3
RTECS  GY5977900
8-10
HS Code  2937500000
NFPA 704
0
2 0

PROSTAGLANDIN A1 price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P7265 Prostaglandin A1 synthetic 14152-28-4 1mg $161 2024-03-01 Buy
Sigma-Aldrich 1578500 Prostaglandin A1 United States Pharmacopeia (USP) Reference Standard 14152-28-4 25mg $3090 2024-03-01 Buy
Cayman Chemical 10010 Prostaglandin A1 ≥98% 14152-28-4 1mg $36 2024-03-01 Buy
Cayman Chemical 10010 Prostaglandin A1 ≥98% 14152-28-4 5mg $120 2024-03-01 Buy
Sigma-Aldrich P7265 Prostaglandin A1 synthetic 14152-28-4 5mg $559 2024-03-01 Buy
Product number Packaging Price Buy
P7265 1mg $161 Buy
1578500 25mg $3090 Buy
10010 1mg $36 Buy
10010 5mg $120 Buy
P7265 5mg $559 Buy

PROSTAGLANDIN A1 Chemical Properties,Uses,Production

Description

Prostaglandin 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.

Uses

Prostaglandin 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.

Definition

ChEBI: Prostaglandin A1 is a prostaglandins A. It is a conjugate acid of a prostaglandin A1(1-).

General Description

Prostaglandin A1(PGA1) belongs to the class of cyclopentenone prostaglandin. PGA1 is generated by the dehydration of prostaglandin E1 (PGE1).

Biochem/physiol Actions

Prostaglandin 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 inhibitor

This 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) Lee et al. (1972) Renal effects of prostaglandin A1 in patients with essential hypertension; Kidney Int. 1 254 2) Toppozada et al. (1988) Treatment of preeclampsia with prostaglandin A1; Am. J. Obstet. Gynecol. 159 160 3) Rossi et al. (2000) Anti-inflammatory cyclopentenone prostaglandins are direct inhibitors of IkappaB kinase; Nature 403 103 4) Mandal et al. (2005), Yin-yang: balancing act of prostaglandins with opposing functions to regulate inflammation; J. Immunol. 175 6271 5) Carta et al. (2014) Prostaglandin A1 inhibits avian influenza virus replication at a postentry level: Effect on virus protein synthesis and NF-kB activity; Prostaglandins Leukot. Essential Fatty Acids 91 311 6) Tsukimoto et al. (2015) A new role for PGA1 in inhibiting hepatitis C virus-IRES-mediated translation by targeting viral translation factors; Antiviral Res. 117 1 7) Diez-Dacal et al. (2011) Identification of aldo-keto reductase AKR1B10 as a selective target for modification and inhibition by prostaglandin A(1): implications for antitumoral activity; Cancer Res. 71 4161 8) Anta et al. (2016), PGA1-induced apoptosis involves specific activation of H-Ras and N-Ras in cellular endomembranes; Cell Death Dis. 7 e2311

PROSTAGLANDIN A1 Preparation Products And Raw materials

Raw materials

Preparation Products

PROSTAGLANDIN A1 Suppliers

Global( 74)Suppliers
Supplier Tel Email Country ProdList Advantage
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Sinoway Industrial co., ltd.
0592-5800732; +8613806035118 xie@china-sinoway.com China 992 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
Sinopharm Chemical Reagent Co,Ltd. 86-21-63210123 sj_scrc@sinopharm.com China 9823 79
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 14059 65
Shanghai Kewel Chemical Co., Ltd. 021-64609169 18901607656 greensnown@163.com China 9911 50
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51471 80
BOC Sciences 16314854226 info@bocsci.com United States 9926 65
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9709 58

View Lastest Price from PROSTAGLANDIN A1 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Prostagladin E1 pictures 2024-04-22 Prostagladin E1
14152-28-4
US $0.00 / Kg/Bag 2Kg/Bag 99% up, High Density 20 tons Sinoway Industrial co., ltd.
PROSTAGLANDIN A1 pictures 2020-02-20 PROSTAGLANDIN A1
14152-28-4
US $1.00 / KG 1KG 99% 200kgs Career Henan Chemical Co
  • Prostagladin E1 pictures
  • Prostagladin E1
    14152-28-4
  • US $0.00 / Kg/Bag
  • 99% up, High Density
  • Sinoway Industrial co., ltd.
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) Prostaglandin Impurity A PGA1 (Prostaglandin A1) prostaglandins A1 synthetic 9-OXO-15S-HYDROXY-PROSTA-10,13E-DIEN-1-OIC ACID [13E,15S]-15-HYDROXY 9-OXOPROSTA-10,13-DIEN-1-OIC ACID PROSTAGLANDINS A1 PROSTAGLANDIN A1 13-dien-1-oicacid,15-hydroxy-9-oxo-,(13e,15s)-prosta-1 2-(3-hydroxy-1-octenyl)-5-oxo-3-cyclopentene-1-heptanoicaci pga(sub1) pga(sup1) prostaglandina(sub1) Prostagladin A Alprostadil (Prostaglandin E1) EP Impurity A Prosta-10,13-dien-1-oic acid, 15-hydroxy-9-oxo-, (13E,15S)- Prostaglandin A1 (1578500) Prostaglandin A Prostagladin E1 PGA1 a.7-[(1R,2S)-2-[(1e,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopent-3-enyl]heptanoicacid(prostaglandina1) Prostaglandin (Alprostadil) EP Impurity A 14152-28-4 33647 BioChemical Biochemicals and Reagents Fatty Acids Prostaglandins Lipids