f2α

Carboprost (15(S)-15-Methyl Prostaglandin F2α) 是一种前列腺素 F2α 的代谢稳定的合成类似物。它能够刺激子宫收缩并引起流产，可用于子宫收缩乏力引起的产后出血，以及在妊娠中期终止妊娠。

Goshonoside F2 是一种从植物中分离到的萜类天然产物。

Labdane F2 is an antagonist of thromboxane B2 and leukotriene B4 isolated from the Spanish herb Sideritis javalambrensis.

Ginsenoside F2 是 Ginsenoside Rb1 的代谢物，通过激活内在的凋亡途径和线粒体功能障碍来诱导乳腺的凋亡，对乳腺癌干细胞具有抗增殖活性。

Icariside F2 shows modest α-glucosidase inhibitory (4.60±1.74% to 11.97±3.30%) and antioxidant activities. It also displays potent NF-κB inhibitory effects, with the IC50 value of 16.25 ± 2.19 uM.

Ginsenoside F2 (Standard) 是 Ginsenoside F2 的标准品。适用于定量分析、质量控制及生化实验等相关研究。Ginsenoside F2 是 Ginsenoside Rb1 的代谢物，通过激活内在的凋亡途径和线粒体功能障碍来诱导乳腺的凋亡，对乳腺癌干细胞具有抗增殖活性。

17-Phenyl trinor prostaglandin F2α glycinamide methyl ester 是Bimatoprost的衍生物，是一种前列腺素类似物和人前列腺素FP受体激动剂，具有眼部降压作用，可用于研究眼高压和青光眼。

16-Phenyl tetranor Prostaglandin F2α (16-Phenyl tetranor PGF2α) 是 PGF2α 的一个代谢稳定类似物。相较于 PGF2α，16-苯基四去甲 PGF2α 对绵羊黄体细胞FP受体的亲和力较低，仅为 8.7%。

20-ethyl Prostaglandin F2α (ICI 74205; 20-ethyl PGF2α) 是 PGF2α 的类似物，也是一种花生四烯酸代谢物。

17-Phenoxy trinor prostaglandin F2α isopropyl ester 是 PGF2α类似物，其为一种口服有效的 PGF 受体 (FPreceptor) 激动剂，并在分娩过程中扮演关键角色。

8-iso Prostaglandin F2α ethanolamide (iPF2α-III ethanolamide; 8-Isoprostane ethanolamide; 8-iso PGF2α ethanolamide) 是一种异前列腺素乙醇酰胺衍生物，由花生四烯乙醇酰胺 (AEA) 经非酶促自由基氧化生成。它通常用于作为氧化应激的标志物，能够区分非酶促分解产物与由COX-2等酶促途径生成的“前列腺酰胺”。

Bimatoprost is the Allergan trade name for 17-phenyl trinor prostaglandin F2α ethyl amide (17-phenyl trinor PGF2α ethyl amide), an F-series PG analog which has been approved for use as an ocular hypotensive drug. Oxidation of the C-15 hydroxyl group produces 15-keto-17-phenyl trinor PGF2α ethyl amide. 15-keto-17-phenyl trinor PGF2α ethyl amide is a potential metabolite of 17-phenyl trinor PGF2α ethyl amide when 17-phenyl trinor PGF2α ethyl amide is administered to intact animals. No pharmacological studies on 15-keto-17-phenyl trinor PGF2α ethyl amide have been reported.

Isoprostanes are produced by the non-enzymatic, free radical peroxidation of phospholipid-esterified arachidonic acid. They have been used as biomarkers of oxidative stress, but they also have been found to have potent biological activity. ent-8-iso-15(S)-Prostaglandin F2α (ent-8-iso-15(S)-PGF2α) is a potent vasoconstrictor of porcine retinal and brain microvessels with EC50 values of 15 and 24 nM, respectively. This isoprostane is about ten-fold more potent than 8-iso-PGF2α in a whole blood platelet aggregation inhibition assay.

ent-Prostaglandin F2α 是 PGF2α 的对映体，在尿液中可被发现。

13,14-dihydro Prostaglandin F2α (13,14-dihydro PGF2α) is the analog of PGF2α which has no unsaturation in the lower side chain. It causes luteolysis in hamsters with a potency five times higher than PGF2α. The ED50 value for 13,14-dihydro PGF2α as a luteolytic agent in hamsters is 1.5 µg/100 g.[1]

15(S)-15-methyl Prostaglandin F2α (15(S)-15-methyl PGF2α) has been shown to have potent uterine stimulant and abortifacient properties when administered intramuscularly to induce labor. 15(S)-15-methyl PGF2α isopropyl ester is a lipophilic analog of 15(S)-15-methyl PGF2α methyl ester, which may be hydrolyzed in vivo to the fully active free acid.

15(S)-15-methyl Prostaglandin F2α methyl ester 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T36156，CAS号为 35700-21-1。

8-iso-13,14-dihydro-15-keto Prostaglandin F2α (8-iso-13,14-dihydro-15-keto PGF2α) is a metabolite of the isoprostane, 8-isoprostane (8-iso PGF2α), in rabbits, monkeys and humans. 8-iso PGF2α is a PG-like product of non-specific lipid peroxidation. In both humans and monkeys, exogenously infused 8-isoprostane is converted primarily to metabolites having 2 or 4 carbon atoms removed from the top side chain by β-oxidation. A similar pattern is observed when tritiated 8-isoprostane is infused into rabbits. Early in the infusion (within 10 minutes) 8-iso-13,14-dihydro-15-keto PGF2α was a significant component of the metabolite profile, which was comprised mostly of dinor 8-isoprostane metabolites. 8-iso-13,14-dihydro-15-keto PGF2α weakly inhibits the U-46619 or collagen-induced aggregation of human platelets, although a number of the E-series isoprostanes are much more potent in this assay.

8-iso-15-keto Prostaglandin F2α (8-iso-15-keto PGF2α) is a metabolite of the isoprostane 8-iso PGF2α in rabbits, monkeys, and humans. 8-isoprostane (8-iso PGF2α) is a prostaglandin-like product of non-specific lipid peroxidation. In both humans and monkeys, exogenously infused 8-iso PGF2α is converted primarily to metabolites having 2 or 4 carbon atoms removed from the top side chain by β-oxidation. A similar pattern is observed when tritiated 8-iso PGF2α is infused into rabbits. Early in the infusion (within 1-2 minutes) 8-iso -15-keto PGF2α was a major component of the metabolite profile, which was comprised mostly of unmetabolized 8-iso PGF2α. 8-iso -15-keto PGF2α is a vasoconstrictor when tested on the rat isolated thoracic aorta, acting via the TP (thromboxane) receptor.

11β-Prostaglandin F2α 是一种由 AKR1C3 催化的生物活性代谢物，可刺激前列腺素 F 受体并诱导乳腺癌中的 slug 表达。11β-Prostaglandin F2α 也是存在于尿液中的内源代谢物。

ent-8-iso Prostaglandin F2α 是猪视网膜和脑微血管的强效血管收缩剂，EC50 值分别为 30.6 和 53.5 nM。

8-Isoprostaglandin F2α 是一种由膜磷脂中花生四烯酸经非酶促过氧化反应生成的异前列腺素，在人血浆中以酯化和游离酸两种形式存在。其在血管平滑肌中作为一种弱的血栓烷类前列腺素受体激动剂发挥作用，被认为是可靠的氧化应激生物标志物。

2,3-dinor-11β-Prostaglandin F2α (2,3-dinor-11β-PGF2α) was recovered from the urine of both normal monkeys and humans when infused with radiolabeled PGD2, where it represented approximately 1% and 4% of the infused radiolabeled dose, respectively. 2,3-dinor-11β-PGF2α has also been recovered from the urine of mastocytosis patients, where it is excreted in large amounts. In human asthmatic patients, 2,3-dinor-11β-PGF2α represents about 40% (as determined by GC/MS) of the immunoreactive 11β-PGF2α when measured using 's 11β-PGF2α EIA Kit . The excretion rate for 2,3-dinor-11β-PGF2α is approximately 200-250 ng/24 hours in a normal adult.

Prostaglandin F2α 1,11-lactone (PGF2α 1,11-lactone) 是前列腺素 F2α 的脂溶性前药，可用于治疗青光眼的研究。 Prostaglandin F2α 1,11-lactone 作为抗生育剂具有活性，可大大降低血管活性。