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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T36770 |
11-deoxy Prostaglandin E1
11-deoxy Prostaglandin E1 |
Others | Others |
11-deoxy Prostaglandin E1 是前列腺素 E1类似物,具有支气管扩张活性,可抑制组胺诱导的支气管收缩,引起离体豚鼠的气管条松弛。 | |||
T36726 |
6-keto Prostaglandin E1
6-keto Prostaglandin E1 |
Others | Others |
6-keto Prostaglandin E1 是 PGE1 的生物活性衍生物,在抗血小板聚集和解聚作用方面发挥作用。 | |||
T36159 |
8-iso Prostaglandin E1
8-iso Prostaglandin E1 |
Others | Others |
8-iso Prostaglandin E1 能引起犬肺静脉中的痉挛,还能够起到血管舒张作用。 | |||
T36775 |
13,14-dihydro Prostaglandin E1
13,14-dihydro Prostaglandin E1 |
Others | Others |
13,14-dihydro Prostaglandin E1 (13,14-dihydro PGE1) is a biologically active metabolite of PGE1 with comparable potency to the parent compound. It is an inhibitor of ADP-induced platelet aggregation in human PRP and washed platelets with IC50 values of 31 and 21 nM, respectively. 13,14-dihydro PGE1 is a slightly more potent inhibitor of ADP-induced human platelet aggregation than PGE1 which has an IC50 value of 40 nM. Also, 13,14-dihydro PGE1 was shown to activate adenylate cyclase in NCB-20 hyb... | |||
T36214 |
16,16-dimethyl Prostaglandin E1
16,16-dimethyl Prostaglandin E1 |
Others | Others |
16,16-dimethyl Prostaglandin E1 是 PGE1 (T1626) 类似物,可诱导支气管收缩和血管平滑肌收缩,并抑制吲哚美辛诱导的细胞伸长。 | |||
T36219 |
1a,1b-dihomo Prostaglandin E1
1a,1b-dihomo Prostaglandin E1 |
Others | Others |
1a,1b-dihomo Prostaglandin E1 是一类前列腺素化合物。 | |||
T84592 |
Prostaglandin E1 ethanolamide
Alprostadil Ethanolamide |
Others | Others |
Prostaglandin E1 ethanolamide,前列腺素E1 (PGE1) 的类似物,可能有效抑制GLI2诱导的靶基因表达(包括Gli1和Ptch1)和肿瘤生长。 | |||
T85025 |
tetranor-Prostaglandin E1
Tetranor PGE1,7α,11-Dihydroxy-5-ketotetranorprost-9-enoic Acid,Tetranorprostaglandin E1 |
Others | Others |
Tetranor-Prostaglandin E1 (tetranor-PGE1), a metabolite of PGE1 and PGE2, undergoes formation through β-oxidation. | |||
T29907 |
Alprostadil sodium
PGE1 sodium salt,Prostaglandin E1 sodium |
Others | Others |
Alprostadil sodium 是一种前列腺素受体配体,对小鼠 EP1、EP2、EP3、EP4和 IP 的 Ki 值分别为 36、10、1.1、2.1 和 33 nM。它诱导血管舒张并抑制血小板聚集,可作为血管扩张剂用于外周血管疾病的研究。 | |||
T37778 |
19(R)-hydroxy Prostaglandin E1
19(R)-hydroxy Prostaglandin E1 |
Others | Others |
19(R)-hydroxy Prostaglandin E1 是 EP1 和 EP3 受体亚型的激动剂,并对平滑肌表现出收缩活性,也是灵长类动物精液中的主要前列腺素。 | |||
T29908 |
Alprostadil ethyl ester
Prostaglandin E1 ethyl ester,PGE1 ethyl ester |
Others | Others |
Alprostadil ethyl ester is a biochemical used in the treatment of scleroderma. | |||
T84595 |
2,3-dinor Prostaglandin E1
2,3-dinor PGE1 |
Others | Others |
Prostaglandin E1 (PGE1), though not predominantly found in nature, plays a significant role in clinical treatments, addressing conditions such as peripheral occlusive vascular disease, erectile dysfunction, and neonatal cardiology issues. The metabolism of PGE1 primarily begins with the oxidation at C-15, producing 13,14-dihydro-15-keto PGE1 as its major metabolite. Alternatively, inhibiting this pathway or overwhelming it with too much PGE1 could potentially enhance the production of 2,3-dinor ... | |||
T25362 |
Ecraprost
AS013,Circulase,AS 013,AS-013,Lipo-pro-prostaglandin E1 |
Others | Others |
Ecraprost is used as a prodrug of prostaglandin E1. | |||
T41323 |
Dihomo-γ-Linolenic acid methyl ester
|
Others | Others |
Dihomo-γ-Linolenic acid methyl ester 是 Dihomo-γ-Linolenic acid 的甲酯形式,Dihomo-γ-Linolenic acid 具有抗炎和抗增殖作用。 | |||
T36147 |
13,14-dihydro-15-keto Prostaglandin E1
13,14-dihydro-15-keto Prostaglandin E1 |
Others | Others |
13,14-dihydro-15-keto Prostaglandin E1 可抑制 ADP 诱导的人离体富血小板血浆中的血小板聚集(IC50=14.8 μg/mL),也是 PGE1 代谢物。 | |||
T84527 |
13,14-dihydro-15(R)-Prostaglandin E1
13,14-dihydro-15(R)-PGE1 |
Others | Others |
13,14-dihydro-15(R)-Prostaglandin E1 (13,14-dihydro-15(R)-PGE1)为13,14-二氢-PGE1的同分异构体,特点在于其C-15位的羟基呈R构型,非自然形态。 | |||
T84513 |
13,14-dihydro-16,16-difluoro Prostaglandin E1
15-hydroxy Lubiprostone |
Others | Others |
Prostaglandin E1 (PGE1), synthesized through cyclooxygenase-mediated metabolism of dihomo-γ-linolenic acid (DGLA), functions by inhibiting platelet aggregation (IC50= 40 nM) and enhancing vasodilation. Its analog, 13,14-dihydro-16,16-difluoro PGE1, and the metabolite, 13,14-dihydro PGE1, both retain similar anti-aggregatory properties to the original compound. The inclusion of two electron-withdrawing fluorine atoms in 13,14-dihydro-16,16-difluoro PGE1 is believed to increase molecular stability... | |||
T84528 |
13,14-dihydro-19(R)-hydroxy Prostaglandin E1
19(R)-hydroxy PGE0 |
Others | Others |
13,14-Dihydro-19(R)-hydroxy Prostaglandin E1 (13,14-dihydro-19(R)-hydroxy PGE1) is posited as a theoretical metabolite resulting from the action of ω-1 hydroxylase on 13,14-dihydro PGE1. Its biosynthesis and biological activity remain unreported in scientific literature. | |||
T20710 |
Ornoprostil
OU-1308,OU 1308,OU1308,Ronoprost |
Others | Others |
Ornoprostil, a prostaglandin E1 analogue, acts as a mucosal protectant. | |||
T84560 |
Prostaglandin A1
PGA1 |
Others | Others |
Prostaglandin A1,Prostaglandin E1的脱水衍生物,具有抑制肿瘤生长、炎症、病毒复制、血小板聚集以及神经毒素诱导的神经元凋亡(apoptosis)的作用。 | |||
T20855 |
Gemeprost
SC-37681,SC 37681,Carprost,Gemeprostum,Cervagem,Preglandin |
Others | Others |
Gemeprost, an analog of prostaglandin E1, is used for the treatment of obstetric bleeding. It is used to terminate pregnancy up to 24 weeks gestation together with mifepristone. | |||
T26090 |
Rioprostil
TR 4698,TR4698,Rioprostilum,TR-4698 |
Others | Others |
Rioprostil is a methyl prostaglandin E1 analog that decreases gastric acid secretion and enhances the gastric mucus-bicarbonate barrier. It is effective in the treatment of gastric ulcers and gives significant protection against NSAID-induced gastric muco | |||
T73346 |
SC 34301
Enisoprost |
Others | Others |
SC 34301 (Enisoprost)为有效的口服活性PGE1类似物,显著降低细菌移位并提升烧伤小鼠存活率。 | |||
T84643 |
Dihomo-γ-Linolenic Acid ethyl ester
ethyl 20:3ω6 |
Others | Others |
Ethyl dihomo-γ-linolenic acid ethyl ester (ethyl DGLA), an ω-6 fatty acid intermediate ester form, elevates prostaglandin E1(PGE1) and PGE2 secretion in rabbit renal papilla when administered dietarily at a dosage of 1 g/kg per day for 25 days. Additionally, this dosage of ethyl DGLA increases triglyceride levels and enhances the proportion of 20:3ω6 and 20:4ω6 phospholipids in the renal medulla of rabbits. Ethyl DGLA formulations have been employed in managing eczema and inflammatory disorders. | |||
T84995 |
1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PA
1-Hexadecanoyl-d9-2-hydroxy-sn-glycero-3-phosphate |
Others | Others |
1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PA (1-palmitoyl-d9LPA) serves as an internal standard for the quantification of 1-palmitoyl LPA using GC- or LC-MS. This compound, an analog of LPA with palmitic acid at the sn-1 position, activates reporter gene expression in PC12 cells fitted with human lysophosphatidic acid receptor 4 (LPA4) at 0.01 to 10 µM concentrations. Additionally, 1-palmitoyl LPA prompts aggregation in isolated human platelets within the 12-300 µM range, a process reversible by pro... | |||
T84609 |
(±)5(6)-DiHET
(±)5,6-DiHETrE |
Others | Others |
5(6)-DiHET is a racemic compound synthesized through the action of epoxide hydrolases on 5(6)-EET, encompassing both enantiomeric forms. It serves as a quantitative marker for 5(6)-EET, facilitating its measurement by utilizing the compound's conversion to 5(6)-δ-lactone in solution. Additionally, 5(6)-DiHET activates large-conductance calcium-activated potassium (KCa1.1/BK) channels in rat small coronary artery smooth muscle cells, supporting its biological significance in vascular regulation. ... | |||
T83807 |
Rp-Adenosine-5'-O-(1-thiotriphosphate) sodium
Rp-ATP-α-S |
Others | Others |
Rp-Adenosine-5'-O-(1-thiotriphosphate)(Rp-ATP-α-S)是一种含硫核苷酸衍生物ATP-α-S的异构体,同时也是嘌呤P2Y1受体的激动剂。在表达人类P2Y1受体的HEK293细胞中,Rp-ATP-α-S能增加钙的动员(EC50 = 75 nM)。该化合物与洗涤的人类孤立血小板结合(Ki = 156 nM),抑制由ADP引发的人类富血小板血浆(PRP)的聚集(pA2 = 4.74),并且能够抑制前列腺素E1(PGE1)在人类孤立PRP中引发的cAMP产生(pA2 = 5.26)。同时,Rp-ATP-α-S还能引起用氨基甲酰胆碱预先缩紧的豚鼠结肠条带的松弛(EC50 = 56 nM)。此外,Rp-ATP-α-S已经被用于合成被细菌核糖开关识别的环状二核苷酸。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1626 |
Prostaglandin E1
前列地尔,PGE1,列腺素E1,Alprostadil |
Endogenous Metabolite; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism |
Prostaglandin E1 (Alprostadil) 是一种前列腺素受体配体,对小鼠 EP1、EP2、EP3、EP4和 IP 的 Ki 值分别为 36、10、1.1、2.1 和 33 nM。它诱导血管舒张并抑制血小板聚集,可作为血管扩张剂用于外周血管疾病的研究。 |