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Cat. No. | Product Name | Target | Signaling Pathways |
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T2280 |
Endoxifen (Z-isomer)
Z-因多昔芬,Endoxifen Z-isomer,4-[(1E)-1-{4-[2-(甲基氨基)乙氧基]苯基}-2-苯基-1-丁烯-1-基]苯酚 |
Estrogen Receptor/ERR; EGFR; Potassium Channel; Estrogen/progestogen Receptor; HER | Angiogenesis; Endocrinology/Hormones; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
Endoxifen Z-isomer (EDX)是 Tamoxifen 重要的代谢产物,在表达 ERα的乳腺癌细胞中发挥抗雌激素作用。它以浓度依赖的方式抑制 hERG, IC50值为1.6μM。 | |||
T11766 |
Eltanexor Z-isomer
KPT-8602 (Z-isomer) |
Others | Others |
Eltanexor Z-isomer exhibits different inhibitory effects on Z138, MM15, 3T3 cell lines, with IC50s of 100 nM-50 μM, < 100 nM, > 30 μM, respectively.Eltanexor Z-isomer is the less active isomer of KPT-8602. KPT-8602 is a potent CRM1 inhibitor. | |||
T6827 |
Endoxifen Z-isomer hydrochloride
Endoxifen HCl,Z-因多昔芬盐酸盐 |
Estrogen Receptor/ERR; Potassium Channel; Estrogen/progestogen Receptor; HER | Angiogenesis; Endocrinology/Hormones; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
Endoxifen Z-isomer hydrochloride (Endoxifen HCl) 是Tamoxifen 最重要的代谢产物, 在表达ERα的乳腺癌细胞中发挥抗雌激素作用, Endoxifen HCl 以浓度依赖的方式抑制hERG, IC50值为1.6μM。 | |||
T1816 |
(Z)-JIB-04
NSC 693627,Z-JIB-04 |
Others | Others |
(Z)-JIB-04 (NSC 693627) 是 JIB-04 的 Z 型异构体。其中 JIB-04 有 E 型和 Z 型异构体两种形式。而(Z)-JIB-04 (NSC 693627) 在表观遗传分析中无活性。 | |||
T0835 |
Tamoxifen Citrate
Tamoxifen Z-isomer citrate,ICI 46474,ICI 46474 Citrate,枸橼酸他莫昔芬,他莫昔芬柠檬酸盐 |
Apoptosis; Estrogen Receptor/ERR; HSP; Estrogen/progestogen Receptor; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; Endocrinology/Hormones; Metabolism |
Tamoxifen Citrate 是一种口服有效的,选择性雌激素受体调节剂,可阻断乳腺细胞中的雌激素作用,并可激活如骨骼、肝脏和子宫细胞中的雌激素活性。它是 Hsp90激活剂,可增强 Hsp90 分子伴侣 ATPase 的活性,可激活自噬和诱导凋亡。 | |||
T11200 |
Endoxifen (E-isomer)
N-去甲-4-羟基-三苯氧胺,E-Endoxifen,Endoxifen E-isomer |
Estrogen Receptor/ERR | Endocrinology/Hormones |
Endoxifen E-isomer (E-Endoxifen) 是一种 Endoxifen 的 E-异构体,是 Endoxifen Z-isomer 原料中主要的杂质。Endoxifen E-isomer 具有抗雌激素活性。 | |||
T16032L |
(Z)-MDL 105519
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Others | Others |
(Z)-MDL 105519是 MDL105519 无活性的异构体。 | |||
T1109 |
(Z)-Capsaicin
Zucapsaicin,Civamide,cis-Capsaicin,珠卡赛辛,(Z)-辣椒素 |
TRP/TRPV Channel; HSV | Membrane transporter/Ion channel; Microbiology/Virology |
(Z)-Capsaicin (Zucapsaicin) 是天然辣椒素的合成顺式异构体,用于治疗膝骨关节炎。它是一种可口服的 TRPV1激动剂,可研究神经性疼痛。 | |||
T13380 |
(Z)-Pitavastatin calcium
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Others | Others |
(Z)-Pitavastatin calcium is the Z-Isomer of Pitavastatin hemicacium. Pitavastatin calcium is a potent of hydroxymethylglutaryl-CoA (HMG-CoA) reductase. | |||
T15186 |
(E)-4-Hydroxytamoxifen
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Others | Others |
(E)-4-Hydroxytamoxifen is a less active isomer of (Z)-4-hydroxytamoxifen and also is an estrogen receptor modulator. | |||
T12611 |
R 80123
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Others | Others |
R 80123 is a highly selective inhibitor of phosphodiesterase,is the Z-isomer of R 79595 | |||
T74028 |
(Z)-2-Octenoic acid
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Z-2-Octenoic acid为2-Octenoic acid的Z-异构体,同时,trans-2-Octenoic acid为Mucor species的代谢产物。 | |||
T35291 |
Z-1,2-Dimethoxy-4-(3-fluoro-2-propenyl)benzene
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Z-1,2-Dimethoxy-4-(3-fluoro-2-propenyl)benzene 是 Methyl eugenol (ME) 的氟类似物,是东方果蝇 B. dorsalis 的引诱剂。E 型异构体的活性是Z型异构体 Z-1,2-Dimethoxy-4-(3-fluoro-2-propenyl)benzene 的两倍。 | |||
T37099 |
(Z)-4EGI-1
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(Z)-4EGI-1 is the Z-isomer of 4EGI-1 and is an inhibitor of eIF4E/eIF4G interaction and of translation initiation. (Z)-4EGI-1 effectively binds to eIF4E with an IC50 of 43.5 μM and a Kd value of 8.74 μM. (Z)-4EGI-1 has anticancer activity[1][2]. [1]. Khuloud Takrouri, et al. Structure-activity Relationship Study of 4EGI-1, Small Molecule eIF4E/eIF4G Protein-Protein Interaction Inhibitors. Eur J Med Chem. 2014 Apr 22;77:361-77. [2]. Poornachandran Mahalingam, et al. Synthesis of Rigidified eIF4E/... | |||
T3645 |
Endoxifen E-isomer hydrochloride
E-Endoxifen hydrochloride |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Endoxifen E-isomer hydrochloride (E-Endoxifen hydrochloride) 是 Endoxifen 的 E-异构体,是 Endoxifen Z-isomer 原料中主要的杂质,具有抗雌激素作用。 | |||
T83878 |
Z-CITCO
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Z-CITCO是构成型雄甾烷受体(CAR;在报告基因测定中,对人类受体的EC50 = 3.9 µM)的激动剂,同时也是CAR激动剂CITCO的顺式异构体。 | |||
T35854 |
9(Z),11(E)-Conjugated Linoleic Acid (sodium salt)
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9(Z),11(E)-Conjugated linoleic acid is an isomer of linoleic acid that has been found in beef and milk fat.1It binds to peroxisome proliferator-activated receptor α (PPARα; IC50= 140 nM) and activates the receptor in a reporter assay using COS-1 cells expressing mouse PPARα when used at a concentration of 100 μM.29(Z),11(E)-Conjugated linoleic acid inhibits TNF-α-inducedGLUT4expression and increases insulin-stimulated glucose transport in 3T3-L1 adipocytes.3Dietary administration of 9(Z)11(E)-co... | |||
T37213 |
5-trans Latanoprost
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Latanoprost is an F-series prostaglandin analog which has been approved for use as an ocular hypotensive drug. 5-trans Latanoprost is an isomer of latanoprost wherein the double bond between carbons 5 and 6 has been changed from cis (Z) to trans (E). The trans isomer of latanoprost occurs as an impurity of between 2-5% in most commercial preparations of the bulk drug product. The present compound was prepared primarily as an analytical standard for detection and quantitation of this impurity. Fr... | |||
T37214 |
5-trans Latanoprost (free acid)
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Latanoprost is an F-series prostaglandin (PG) analog which has been approved for use as an ocular hypotensive drug. Latanoprost is an isopropyl ester, a prodrug form which is converted to latanoprost (free acid) by endogenous esterase enzymes. The free acid form is 200 times more potent than latanoprost as a ligand for the human recombinant FP receptor. 5-trans Latanoprost (free acid) is an isomer of latanoprost (free acid) wherein the double bond between carbons 5 and 6 has been changed from ci... | |||
T36608 |
(±)8-HEPE
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(±)8-HEPE is produced by non-enzymatic oxidation of EPA. It contains equal amounts of 8(S)-HEPE and 8(R)-HEPE. The ability of (±)8-HEPE to induce hatching of E. modestus and B. balanoides eggs is probably due to the presence of the 8(R) isomer within the racemic mixture.[1][2] Reference:[1]. Shing, T.K.M., Gibson, K.H., Wiley, J.R., et al. First total synthesis of a barnacle hatching factor 8(R)-hydroxy-eicosa-5(Z),9(E),11(Z)-pentaenoic acid. Tetrahedron Letters 35, 1067-1070 (1994).[2]. Hill, E... | |||
T36887 |
8(E),10(E),12(Z)-Octadecatrienoic Acid
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8(E),10(E),12(Z)-Octadecatrienoic acid is a conjugated polyunsaturated fatty acid (PUFA) that has been found inC. officinalisseed oil and has anticancer activity.1,2,3It inhibits the growth of Caco-2 cells when used at concentrations ranging from 10 to 50 μM.28(E),10(E),12(Z)-Octadecatrienoic acid (10 μM) induces formation of thiobarbituric acid reactive substances (TBARS) and apoptosis in DLD-1 colorectal adenocarcinoma cells.3It also inhibits prostaglandin biosynthesis in sheep vesicular gland... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T8137 |
(Z)-Aconitic acid
顺乌头酸,顺式乌头酸,Cls-Aconitic acid |
Others; Endogenous Metabolite | Metabolism; Others |
(Z)-Aconitic acid 是 Aconitic acid 的顺式异构体。它是三羧酸循环中柠檬酸盐异构化为异柠檬酸盐的中间产物。 |