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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
TDS File:
TDS
Last updated:2026-05-28 03:58:37
Product description Number Pack Size Price
Prostaglandin A1 synthetic P7265 1mg $178
Prostaglandin A1 United States Pharmacopeia (USP) Reference Standard 1578500 25mg $3310
Prostaglandin A1 ≥98% 10010 1mg $50
Prostaglandin A1 ≥98% 10010 5mg $174
Prostaglandin A1 ≥98% 10010 10mg $297

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
biological source synthetic
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.
InChI 1S/C20H32O4/c1-2-3-6-9-17(21)14-12-16-13-15-19(22)18(16)10-7-4-5-8-11-20(23)24/h12-18,21H,2-11H2,1H3,(H,23,24)/b14-12+/t16-,17-,18+/m0/s1
InChIKey BGKHCLZFGPIKKU-LDDQNKHRSA-N
SMILES O=C1[C@H](CCCCCCC(O)=O)[C@@H](/C=C/[C@H](CCCCC)O)C=C1
FDA UNII VYR271N44P
UNSPSC Code 12352211
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
Signal word  Danger
Hazard statements  H302-H360F
Precautionary statements  P201-P301+P312+P330-P308+P313
PPE Eyeshields, Gloves, type N95 (US)
Safety Statements  22-24/25
WGK Germany  3
RTECS  GY5977900
8-10
HS Code  2937500000
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 4 Oral
Repr. 1B
NFPA 704
0
2 0

PROSTAGLANDIN A1 price More Price(37)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P7265 Prostaglandin A1 synthetic 14152-28-4 1mg $178 2026-04-30 Buy
Sigma-Aldrich 1578500 Prostaglandin A1 United States Pharmacopeia (USP) Reference Standard 14152-28-4 25mg $3310 2026-04-30 Buy
Cayman Chemical 10010 Prostaglandin A1 ≥98% 14152-28-4 1mg $50 2026-04-30 Buy
Cayman Chemical 10010 Prostaglandin A1 ≥98% 14152-28-4 5mg $174 2026-04-30 Buy
Cayman Chemical 10010 Prostaglandin A1 ≥98% 14152-28-4 10mg $297 2026-04-30 Buy
Product number Packaging Price Buy
P7265 1mg $178 Buy
1578500 25mg $3310 Buy
10010 1mg $50 Buy
10010 5mg $174 Buy
10010 10mg $297 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 Bergstrm 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

Raw materials

Preparation Products

PROSTAGLANDIN A1 Suppliers

Global( 97)Suppliers
Supplier Tel Email Country ProdList Advantage
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58
HANGZHOU LEAP CHEM CO., LTD.
+86-571-87711850 market18@leapchem.com China 43333 58
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 20122 58
Aladdin Scientific
tp@aladdinsci.com United States 57505 58
SHANGHAI KEAN TECHNOLOGY CO., LTD.
+8613817748580 cooperation@kean-chem.com China 40066 58
Sinoway Industrial co., ltd.
+86-0592-5800732 +86-13806035118 xie@china-sinoway.com China 1369 58
Sinopharm Chemical Reagent Co,Ltd. 86-21-63210123 sj_scrc@sinopharm.com China 9815 79
Shanghai Macklin Biochemical Co.,Ltd. 15221275939; 15221275939 shenlinxing@macklin.cn China 15781 55
Shanghai Kewel Chemical Co., Ltd. 021-64609169 18901607656 greensnown@163.com China 9906 50
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51395 80

View Lastest Price from PROSTAGLANDIN A1 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Prostagladin E1 pictures 2026-06-03 Prostagladin E1
14152-28-4
2Kg/Bag 99% up, High Density 20 tons Sinoway Industrial co., ltd.
PROSTAGLANDIN A1 pictures 2020-02-20 PROSTAGLANDIN A1
14152-28-4
$1.00 1KG 99% 200kgs Career Henan Chemical Co
  • Prostagladin E1 pictures
  • Prostagladin E1
    14152-28-4
  • $0.00
  • 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)- Prostagladin E1 Prostaglandin A1 (1578500) Prostaglandin (Alprostadil) EP Impurity A a.7-[(1R,2S)-2-[(1e,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopent-3-enyl]heptanoicacid(prostaglandina1) Prostaglandin A1 PGA1 Prostaglandin A 14152-28-4 33647 BioChemical Biochemicals and Reagents Fatty Acids Prostaglandins Lipids