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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T41215 |
LC 2 Epimer
|
Others | Others |
Negative control for LC 2. | |||
T71048 |
Tacrolimus anhydrous 8-epimer
|
Others | Others |
Tacrolimus anhydrous 8-epimer is a new l-pipecolic acid macrolide lactone, an important immunosuppressive drug that blocks T cell proliferation in vitro by inhibiting the generation of several lymphokines, especially IL-2. | |||
T26330 |
WIN 5063-3
WIN-5063-3,Thiamphenicol epimer,WIN5063-3,L-Thiamphenicol |
Others | Others |
WIN 5063-3 is the enantiomeric analog of the antimicrobial Thiamphenicol. | |||
T75390 |
Aldose 1-epimerase
|
Others | Others |
Aldose 1-epimerase (mutarotases) 是关键碳水化合物代谢酶,主要催化己糖如葡萄糖及半乳糖的α-与β-端基异构体互转。对于碳水化合物代谢及复杂寡糖生成至关重要。 | |||
T8339 |
16α-Hydroxyprednisolone
16alpha-羟基泼尼松龙,16alpha-Hydroxyprednisolone |
Others; Drug Metabolite | Metabolism; Others |
16α-Hydroxyprednisolone 是糖皮质激素布地奈德 22(R) epimer 构型的代谢物,经过 CYP3A 酶代谢生成。 | |||
T10132 |
(3S,5S)-Pitavastatin calcium
|
Others | Others |
(3S,5S)-Pitavastatin calcium is the 3-epimer of Pitavastatin which is a potent HMG-CoA reductase inhibitor. | |||
T19299 |
DTE
Cleland’s reagent,Dithioerythritol |
Others | Others |
Dithioerythritol (DTE), a sulfur-containing sugar derivative of the 4-carbon monosaccharide erythrose, is an epimer of dithiothreitol (DTT). | |||
T84644 |
15(S)-Fluprostenol isopropyl ester
15(S)-Flu-Ipr |
Others | Others |
15(S)-Fluprostenol isopropyl ester, an isomer of the prostaglandin F2α analog, fluprostenol isopropyl ester, serves as a possible prodrug to 15(S)-fluprostenol. It has the potential to act as an agonist at FP receptors, albeit with lower potency compared to the 15(R) epimer and the FP receptor agonist, fluprostenol. Additionally, it may be present as a potential impurity in commercial formulations of fluprostenol isopropyl ester. | |||
T36043 |
17(R)-Protectin D1
17(R)-Protectin D1 |
Others | Others |
17(R)-Protectin D1 is an aspirin-triggered epimer of the specialized pro-resolving mediator protectin D1 .1It decreases leukotriene B4-induced transendothelial migration of human polymorphonuclear (PMN) neutrophils when used at concentrations ranging from 0.1 to 10 nM. 17(R)-Protectin D1 (0.01-10 ng) reduces the recruitment of neutrophils in a mouse model of TNF-α-induced peritonitis. 1.Serhan, C.N., Fredman, G., Yang, R., et al.Novel proresolving aspirin-triggered DHA pathwayChem. Biol.18(18)97... | |||
T85200 |
17(R)-Resolvin D4
4(S),5(R),17(R)-trihydroxy-DHA,17(R)-RvD4 |
Others | Others |
17(R)-Resolvin D4 (17(R)-RvD4) is an epimer of RvD4, generated through the aspirin-induced modification process. | |||
T82805 |
Butaprost free acid
|
Others | Others |
(R)-Butaprost (free acid) 是PGE2的一个结构类似物,特异性地对EP2受体亚型有选择性。该化合物用于药理学研究,以确定不同人类及动物组织和细胞中EP受体的分布。去除甲酯基团并恢复C-1自然羧酸后,增强了(R)-butaprost与前列腺素受体的结合亲和力,通常情况下,游离酸形式的亲和力是相应酯形式的10到100倍。尽管(R)-butaprost作为C-16的较低活性差向异构体,其药理作用未经充分研究,但在1986年Gardiner的论文中提到的TR 4979即布他前列素,结构中的差向异构体错误表达为16(R),实际为16(S),该错误直至1990年代后期才被美国和日本的研究纠正。 | |||
T37001 |
7-epi Maresin 1
|
Others | Others |
7-epi Maresin 1 is the inactive 7(S) epimer of Maresin 1 , which contains a 7(R) hydroxyl group. It can be used as an experimental negative control. | |||
T36595 |
4-epi-Chlortetracycline (hydrochloride)
|
Others | Others |
Chlortetracycline is an analog of tetracycline , a broad spectrum antibiotic. In addition to its actions against microorganisms, chlortetracycline suppresses inflammation by inhibiting neutrophil action and other aspects of the innate immune response. 4-epi-Chlortetracycline is an epimer of chlortetracycline. | |||
T37965 |
4-Epitetracycline hydrochloride
|
Others | Others |
Epitetracycline is an epimer of the antibiotic tetracycline . Epimers of tetracycline form without catalysis and are considered degradation products. Epitetracycline has decreased activity as an antibiotic or a Tet repressor effector but may have stronger toxic effects in animals. | |||
T37649 |
5(S),12(S)-DiHETE
|
Others | Others |
5(S),12(S)-DiHETE is a natural bioactive lipid derived from arachidonic acid . It is synthesized by glycogen-induced rabbit peritoneal polymorphonuclear leukocytes (PMNLs) incubated with AA. 5(S),12(S)-DiHETE can be produced by successive oxygenation of AA by 5-lipoxygenase (5-LO) in platelets and 12-LO in leukocytes. It can also be synthesized from 12(S)-HETE by 5-LO, in the presence of 5-LO activating protein (FLAP), activated with calcium ionophore. 5(S),12(S)-DiHETE is an epimer of leukotrie... | |||
T35500 |
3-epi-25-hydroxy Vitamin D3
3-epi-25-hydroxy Vitamin D3 |
Others | Others |
3-epi-25-hydroxy Vitamin D3is the C-3 epimer of 25-hydroxy vitamin D3.1Dietary administration of 3-epi-25-hydroxy vitamin D3(0.5 and 1 IU/g) decreases levels of serum parathyroid hormone (PTH) in male, but not female, weanling rats. 1.Djekic-Ivankovic, M., Lavery, P., Agellon, S., et al.The C-3α epimer of 25-hydroxycholecalciferol from endogenous and exogenous sources supports normal growth and bone mineral density in weanling ratsJ. Nutr.147(2)141-151(2017) | |||
T84559 |
15(S)-Fluprostenol
|
Others | Others |
15(S)-Fluprostenol, an isomer of the FP receptor agonist fluprostenol, serves as a potential active metabolite of 15(S)-fluprostenol isopropyl ester. It can function as an agonist at FP receptors, though with lower potency compared to its 15(R) epimer, fluprostenol. | |||
T84944 |
3-Epideoxycholic Acid
EDCA |
Others | Others |
3-Epideoxycholic acid (EDCA), a secondary bile acid and an epimer of deoxycholic acid, serves as a steroidal host compound in the enantioselective purification of (2R,3S)-3-methyl-2-pentanol from its racemates via enclathration. Additionally, decreased fecal levels of EDCA have been observed in pediatric patients with non-alcoholic fatty liver disease (NAFLD). | |||
T84624 |
8-iso-15(R)-Prostaglandin F2α
8-iso-15-epi PGF2α |
Others | Others |
8-iso-15(R)-Prostaglandin F2α (8-iso-15(R) PGF2α) is a chemically distinct member within a broad group of prostaglandin-like eicosanoids, produced through the free radical peroxidation of arachidonic acid contained in membrane phospholipids. It represents the C-15 epimer of 8-isoPGF2α, distinguished as the sole isoprostane isomer extensively examined across numerous biological systems. | |||
T36208 |
15(R)-Pinane Thromboxane A2
15(R)-Pinane Thromboxane A2 |
Others | Others |
15(R)-Pinane thromboxane A2 is the (R)-epimer of pinane thromboxane A2 . 15(R)-PTA2 does not inhibit collagen-induced platelet aggregation (IC50s = 120-130 μM). It does not affect gastric tone in isolated rat gastric fundus when used at concentrations of 0.5 or 1.5 μg/ml and is less effective than PTA2 at inhibiting prostaglandin-induced contraction of isolated rat stomach muscle. | |||
T36144 |
11β-Prostaglandin E2
11β-PGE2,11β-Prostaglandin E2 |
Others | Others |
11β-PGE2 is the C-11 epimer of PGE2. It is a moderate inhibitor of PGE2 binding to rat hypothalamic membranes with a Ki value of 53 nM.[1] 11β-PGE2 also stimulates bone resorption in rats at concentrations of 10-8 to 10-6 M which is similar to PGE2.2 11β-PGE2 inhibits PGE2 binding to the prostaglandin transporter protein with a Ki of 56 nM.[3] . | |||
T84455 |
17(R)-Resolvin D1 methyl ester
Aspirin-triggered-Resolvin D1 methyl ester |
Others | Others |
17(R)-Resolvin D1 (17(R)-RvD1) is an aspirin-triggered epimer of RvD1 that equivalently inhibits human polymorphonuclear leukocyte migration across the endothelium (EC50= ~30 nM), a precursor to acute inflammation. Unlike RvD1, it resists rapid degradation by eicosanoid oxidoreductases. In a mouse peritonitis model, 17(R)-RvD1 dose-dependently reduces leukocyte infiltration, achieving up to a 35% decrease with a 100 ng dose. Additionally, its methyl ester derivative, designed to enhance its phar... | |||
T84587 |
15(R)-Prostaglandin E2
15-epi PGE2 |
Others | Others |
15(R)-Prostaglandin E2, the C-15 epimer of the more physiologically abundant 15(S)-PGE2 (sc-201225) isomer, is produced mainly from arachidonic acid (sc-200770) via the action of COX and PGES enzymes. Present in nearly all cell types, PGE2 interacts with four distinct receptors, EP1 to EP4, leading to a wide range of biological effects. However, 15(R)-Prostaglandin E2 exhibits significantly lower efficacy in most biological assays compared to its 15(S) counterpart. Notably, acid catalyzed epimer... | |||
T84598 |
15(R),19(R)-hydroxy Prostaglandin F2α
15(R),19(R)-hydroxy PGF2α |
Others | Others |
19(R)-Hydroxylated prostaglandins (PGs) are present at µg/ml concentrations in the semen of some mammalian species, notably primates, with the majority being from the PGE series and featuring a 15(S),19(R) hydroxyl stereochemistry. These compounds are also observed in marsupials' seminal plasma, where F-type 1 and 2-series compounds are predominant. The 15(R)-hydroxy epimer represents the inverse or "unnatural" isomer at C-15 for these 19-hydroxylated PGs. Although the biological function of 19(... | |||
T85108 |
17(R)-Resolvin D3
Aspirin-triggered Resolvin D3,AT-RvD3,17(R)-RvD3,17-epi-Resolvin D3 |
Others | Others |
17(R)-Resolvin D3 (17(R)-RvD3) is an aspirin-triggered epimer of resolvin D3, produced from docosahexaenoic acid (DHA) through the action of COX-2 in the presence of aspirin, via a 17(R)-hydroperoxy DHA (17(R)-HDHA) intermediary. Identified in mouse inflammatory exudates, 17(R)-RvD3 notably inhibits the transmigration of isolated human polymorphonuclear cells (PMNs) and fosters the efferocytosis of apoptotic PMNs by macrophages. Furthermore, in a mouse model of zymosan-induced peritonitis, 17(R)... | |||
T35946 |
17(R)-Resolvin D1
Aspirin-triggered Resolvin D1,17(R)-Resolvin D1 |
Others | Others |
Resolvins are a family of potent lipid mediators derived from both eicosapentaenoic acid and docosahexaenoic acid.[1] In addition to being anti-inflammatory, resolvins promote the resolution of the inflammatory response back to a non-inflamed state.[2] Resolvin D1 is produced physiologically from the sequential oxygenation of DHA by 15- and 5-lipoxygenase.[1] 17(R)-RvD1 is an aspirin-triggered epimer of RvD1 that reduces human polymorphonuclear leukocyte (PMN) transendothelial migration, the ear... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3828 |
(-)-Gallocatechin
(2S,3R)-gallocatechin,(−)-GC,(-)-棓儿茶酸;没食子儿茶素,没食子儿茶素 |
Others | Others |
(-)-Gallocatechin ((−)-GC) 是一种 (-)-Epigallocatechin (EGC) 的差向异构体,常存在于各种茶产品中,具有抗氧化特性。 | |||
T5915 |
D-chiro-Inositol
D-手性肌醇,D-(+)-CHIRO-INOSITOL |
Endogenous Metabolite | Metabolism |
D-chiro-Inositol (D-(+)-CHIRO-INOSITOL) 是肌醇差向异构体,存在于某些哺乳动物糖基磷脂酰肌醇蛋白锚和具有胰岛素样生物特性的肌醇磷脂聚糖中。它能够抑制高血糖,改善胰岛素抵抗。它用于多囊卵巢综合征和糖尿病的相关研究。 | |||
TN7414 |
10-Deacetylcephalomannine
|
Others | Others |
10-Deacetylcephalomannin exhibits activity against PS leukemia in vivo; however, its instability leads to an equilibrium mixture with its cytotoxic C-7 epimer. Additionally, 10-Deacetylcephalomannine demonstrates growth inhibitory effects on human cancer cell lines, including cervical HeLa adenocarcinoma. | |||
TN6799 |
Epiprogoitrin
表原告依春,epi-Progoitrin |
Others | Others |
Epiprogoitrin (epi-Progoitrin) 是一种硫代葡萄糖苷,来自于Crambe abyssinica 种子。 | |||
T81318 |
R-30-Hydroxygambogic acid
|
||
R-30-Hydroxygambogic acid是从藤黄提取的一种聚戊烯酰黄酮外聚体,对K562/R和K562/S两种人白血病细胞系的IC50分别为2.89 μM和1.27 μM。该化合物适用于癌症研究领域。 | |||
T75631 |
Ganorbiformin B
|
Others | Others |
Ganorbiformin B是一种具有与灵芝酸相同羊毛甾烷骨架的羊毛甾烷三萜类化合物。其C-3差向异构体灵芝酸T对结核分枝杆菌H37Ra显示出强抗分枝杆菌活性。 | |||
T81232 |
S-30-Hydroxygambogic acid
|
||
S-30-Hydroxygambogic acid,一聚戊烯酰黄酮外聚体,源自藤黄。针对人白血病细胞系K562/R及K562/S,其IC50值别为4.49 μM与3.61 μM。S-30-Hydroxygambogic acid主用于癌症研究领域。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIH-0039 |
3 Hydroxy Midostaurin Epimer 2-d5
CGP52421 Epimer 2-d5 |
||
3 Hydroxy Midostaurin Epimer 2-d5 是 3 Hydroxy Midostaurin Epimer 2 的氘代化合物。3 Hydroxy Midostaurin Epimer 2 的 CAS 号为 155848-20-7。 | |||
TMIH-0038 |
3 Hydroxy Midostaurin Epimer 1-d5
CGP52421 Epimer 1-d5 |
||
3 Hydroxy Midostaurin Epimer 1-d5 是 3 Hydroxy Midostaurin Epimer 1 的氘代化合物。3 Hydroxy Midostaurin Epimer 1 的 CAS 号为 945260-14-0。 |