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30
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T22884 |
JW 67
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
JW 67 是典型 Wnt 信号通路的抑制剂,IC50为 1.17 μM。它影响由 β- 连环蛋白/GSK-3β/AXIN/APC/CK1 组成的多蛋白复合物,快速降低活性 β- 连环蛋白,随后下调Wnt 靶基因。它也抑制结直肠癌细胞生长。 | |||
TP2068L |
Cyclotraxin B acetate(1203586-72-4 free base)
|
Trk receptor | Tyrosine Kinase/Adaptors |
Cyclotraxin B acetate(1203586-72-4 free base) 是 TrkB 受体的拮抗剂;抑制 BDNF 诱导的 TrkB 活性 (IC50 = 0.30 nM)。变构改变 TrkB 受体构象但不改变 BDNF 结合。防止 BDNF 引起的小鼠冷异常性疼痛。还显示在小鼠中表现出推定的抗焦虑特性。 | |||
T22453 |
Venlafaxine
Wy 45030,文拉法辛 |
Serotonin Transporter | Neuroscience |
Venlafaxine (Wy 45030) 是一种口服有效的 5-羟色胺 (5-HT)/去甲肾上腺素 (NE) 重摄取的双重抑制剂,具有抗抑郁活性。 | |||
T5380 |
Ansofaxine hydrochloride
Ansofaxine盐酸盐,LPM570065,LY03005 |
Dopamine Receptor; 5-HT Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Ansofaxine hydrochloride (LY03005) 是一种血清素-去甲肾上腺素-多巴胺再摄取抑制剂,IC50值分别为723、491 和 763 nM。 | |||
T2064 |
Semaxinib
司马沙尼,SU5416 |
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Semaxinib (SU5416) 是一种选择性的 VEGFR(Flk-1/KDR) 抑制剂,其 IC50=1.23 μM。 | |||
T0472 |
Venlafaxine hydrochloride
Venlafaxine HCl,盐酸文拉法辛,Wy 45030 hydrochloride |
5-HT Receptor; Serotonin Transporter | GPCR/G Protein; Neuroscience |
Venlafaxine hydrochloride (Wy 45030 hydrochloride) 是一种口服有效的 5-羟色胺 (5-HT)/去甲肾上腺素 (NE) 重摄取的双重抑制剂,具有抗抑郁活性。 | |||
T2496 |
(Z)-Semaxinib
SU5416 |
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
(Z)-Semaxinib (SU5416) 是一种有效的选择性 VEGFR(Flk-1/KDR) 抑制剂 (IC50: 1.23 μM),对 VEGFR 的选择性是 PDGFRβ 的 20 倍,对 FGFR、InsR 和 EGFR 没有抑制作用。 Semaxanib 是一种具有潜在抗肿瘤活性的喹诺酮衍生物。 | |||
T10415 |
Autotaxin-IN-3
|
PDE | Metabolism |
Autotaxin-IN-3 是 Autotaxin 的抑制剂(IC50 = 2.4 nM),Autotaxin 负责增加腹水和血浆中的溶血磷脂酸。 | |||
T6188 |
Desvenlafaxine succinate hydrate
O-Desmethylvenlafaxine succinate hydrate,WY 45233 Succinate,琥珀酸去甲文拉法辛,Desvenlafaxine Succinate |
5-HT Receptor; Serotonin Transporter; Norepinephrine | GPCR/G Protein; Neuroscience |
Desvenlafaxine succinate hydrate (WY 45233 Succinate) 是 Venlafaxine 主要代谢物的丁二酸盐形式,在人多巴胺转运体上显示弱的结合亲和力。它是具有口服活性的、能透过血脑屏障的5-HT 和 去甲肾上腺素再摄取的抑制剂,对 hSERT 和 hNET 的IC50值分别为47.3 nM 和531.3 nM。 | |||
T10416 | Autotaxin-IN-4 | PDE | Metabolism |
Autotaxin-IN-4 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis. | |||
T60508 |
(S)-Venlafaxine
|
||
(S)-Venlafaxine 是 Venlafaxine 的(S)-构型。Venlafaxine 是一种具有口服活性的 5-羟色胺 (5-HT)/去甲肾上腺素 (NE) 再摄取双重抑制剂, 具有抗抑郁活性。 | |||
T10418 | Autotaxin modulator 1 | PDE | Metabolism |
Autotaxin modulator 1 is a new modulator of Autotaxin. | |||
T10417 |
Autotaxin-IN-5
|
PDE | Metabolism |
Autotaxin-IN-5 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis. | |||
T72837 | Autotaxin-IN-6 | ||
Autotaxin-IN-6 (compound 23),一种ATX (自分泌运动分子)抑制剂,具有30 nM的IC50值,能够减少细胞迁移,适用于抗癌研究。 | |||
T38134 |
(S)-O-Desmethyl Venlafaxine N-Oxide
|
||
(S)-O-Desmethyl Venlafaxine N-Oxide, an N-oxide derivative of (S)-O-Desmethyl Venlafaxine, constitutes an active metabolite of the serotonin-norepinephrine reuptake inhibitor (SNRI) class antidepressant, Venlafaxine[1][2]. | |||
T73977 | (S)-Dehydro Venlafaxine | ||
(S)-Dehydro Venlafaxine 是 Dehydro Venlafaxine 的非活性 S-对映异构体。Dehydro Venlafaxine 是 Venlafaxine 的杂质。Venlafaxine (Wy 45030) 是有效的 5-羟色胺 (5-HT) / 去甲肾上腺素 (NE) 再摄取双重抑制剂。 | |||
TP2068 |
Cyclotraxin B
|
||
Antagonist of TrkB receptors; inhibits BDNF-induced TrkB activity (IC50 = 0.30 nM). Allosterically alters TrkB receptor conformation but does not alter BDNF binding. Prevents BDNF-induced cold allodynia in mice. Also shown to exhibit putative anxiolytic p | |||
T41060 |
Ansofaxine
Ansofaxine,LPM570065freebase,Toludesvenlafaxine,LY03005freebase |
||
Ansofaxine, an SNRI compound, is commonly utilized in depression research as a serotonin-norepinephrine reuptake inhibitor. | |||
T1580 |
Desvenlafaxine
去甲文拉法辛,WY 45233 Succinate,O-Desmethylvenlafaxine |
5-HT Receptor; Serotonin Transporter; Norepinephrine | GPCR/G Protein; Neuroscience |
Desvenlafaxine (O-Desmethylvenlafaxine) 是 Venlafaxine 主要代谢物的丁二酸盐形式,在人多巴胺转运体上显示弱的结合亲和力。它是一种具有口服活性的、能透过血脑屏障的5-HT 和去甲肾上腺素再摄取的抑制剂,对 hSERT 和 hNET 的IC50值分别为 47.3 nM 和 531.3 nM。 | |||
T80447 |
Pardaxin P5
|
||
Pardaxin P5,一种抗菌肽,其对大肠杆菌的最小抑制浓度(MIC)为13 μM。 | |||
T81300 |
Relaxin H3 (human)
|
||
Relaxin H3 (human)为一类松弛素肽,通过与RXFP1受体结合来发挥其抗纤维化的生物学功能。 | |||
TP2404 |
Relaxin C-peptide
Relaxin (79-92) |
||
Relaxin C-peptide, as a synthetic 14-amino acid peptide found in human decidua & placenta, can represent a partial sequence of human relaxin connecting peptide. | |||
T75832 |
Cyclotraxin B TFA
|
||
Cyclotraxin B TFA 是一种环肽,是一种高效且选择性的 TrkB 抑制剂,且不会改变 BDNF 的结合。Cyclotraxin B TFA 非竞争性地抑制 BDNF 诱导的 TrkB 活性,IC50值为 0.30 nM。Cyclotraxin B TFA 可以穿越血脑屏障,并具有止痛和抗焦虑的行为作用。 | |||
T14352 |
Autotaxin-IN-1
|
PDE | Metabolism |
Autotaxin-IN-1 is a potent autotaxin inhibitor, which has favorable potency (IC50=2.2 nM), PK properties, and a robust PK/PD relationship and it is used in treatment of osteoarthritis pain[1]. | |||
T30237 |
Axinylsterol
|
||
Axinylsterol is a biochemical. | |||
T27976 |
Manifaxine
BW1555U88,BW-1555U-88,1555U88,1555U-88,GW-320659,GW320659 |
||
Manifaxine, a norepinephrine-dopamine reuptake inhibitor, is used potentially for the treatment of attention deficit. | |||
T11571 |
HLY78
4-Ethyl-5-methyl-5,6-dihydro-[1,3]dioxolo[4,5-j]phenanthridine |
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
HLY78 (4-Ethyl-5-methyl-5,6-dihydro-[1,3]dioxolo[4,5-j]phenanthridine) 是 Wnt/β-catenin 信号通路的激活剂,通过靶向通道中 Axin 的 DIX 域,增强 Axin-LRP6 交联,诱导 Wnt 信号转导。 | |||
T6989 |
SKL2001
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
SKL2001 是一种Wnt/β-catenin 信号通路的激动剂,具有抗肿瘤作用。它能够破坏 Axin/β-catenin 相互作用,稳定细胞内 β-catenin。 | |||
T2651 |
IWR-1
IWR-1-endo,endo-IWR 1 |
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
IWR-1 (IWR-1-endo) 是一种 Wnt 通路抑制剂,可稳定 Axin 破坏复合物 (EC50=0.2 uM)。 | |||
T35550 |
FRATide
|
||
FRATtide 可抑制 Axin 和 β-catenin 的磷酸化,抑制 GSK-3 结合 Axin,是一种源自 GSK-3 结合蛋白的肽。 | |||
T27760 | KYA1797 | ||
KYA1797 is an inhibitor of the Wnt/ß-catenin pathway. KYA1797 binds directly to the regulators of G-protein signaling domain of axin, initiats ß-catenin and Ras degradation through enhancement of the ß-catenin destruction complex activating GSK3ß, effecti | |||
T69880 | YW2065 | ||
YW2065 has excellent anti-colorectal cancer effects in vitro and in vivo. YW2065 achieves its inhibitory activity for Wnt signaling by stabilizing Axin-1, a scaffolding protein that regulates proteasome degradation of β-catenin. Simultaneously, YW2065 also led to the activation of the tumor suppressor AMPK, providing an additional anticancer mechanism. In addition, YW2065 showed favorable pharmacokinetic properties without obvious toxicity. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3366 |
Cephalotaxine
ZINC19795976,三尖杉碱,(-)-Cephalotaxine,Cephalotaxlen |
Antiviral; Influenza Virus | Immunology/Inflammation; Microbiology/Virology |
Cephalotaxine (ZINC19795976) 是从头孢紫杉中分离得到的一种生物碱,具有抗白血病和抗病毒活性,如抗 Zika 病毒。 | |||
T3818 |
Fraxinol
|
Others; P450 | Metabolism; Others |
Fraxinol 是一种分离自半边莲中的化合物。 | |||
T9358 |
N,N,O-Tridesmethylvenlafaxine
Tridesmethylvenlafaxine |
Others; Endogenous Metabolite | Metabolism; Others |
N,N,O-Tridesmethylvenlafaxine (Tridesmethylvenlafaxine) 是内源性代谢产物的一种。 | |||
T3783 |
Fraxin
Fraxoside,Fraxetin-8-O-glucoside,Paviin,秦皮甙 |
OAT; transporter; PDE | Membrane transporter/Ion channel; Metabolism |
Fraxin (Fraxoside) 是一种白蜡树内酯的糖苷,可从Acer tegmentosum,F. ornus 和A. hippocastanum 等分离得到,具有抗氧化、抗炎和抗转移活性。它能够抑制环腺苷酸磷酸二酯酶,具有抗氧化作用。 | |||
T6S0071 |
Fraxinellone
|
HIF/HIF Prolyl-Hydroxylase; STAT; PD-1/PD-L1 | Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Metabolism; Stem Cells |
Fraxinellone 是从白鲜的根皮中分离出来的一种天然产物,是PD-L1抑制剂,可抑制HIF-1α蛋白质合成。它通过靶向 PD-L1,有用于癌症免疫的潜力。 | |||
TN3315 |
9-Deacetyltaxinine E
|
Others | Others |
9-Deacetyltaxinine E is a natural product from Taxus mairei. | |||
T28834 |
Spirolaxine
|
||
Spirolaxine, a natural product isolated from Sporotrichum laxum ATCC 15155, has shown a variety of biological activities including promising anti-Helicobacter pylori property. | |||
TN5113 |
Taxinine B
|
Others | Others |
Taxinine and taxinine B can inhibit the drug transport by P-glycoprotein in multidrug-resistant cells. Taxinine B shows stronger inhibitory effects than acetylsalicylic acid (ASA) on platelet aggregation induced by arachidonic acid (AA). | |||
TN5114 |
Taxinine
|
P-gp | Membrane transporter/Ion channel; Neuroscience |
Taxinine and Taxinine B can inhibit the drug transport by P-glycoprotein in multidrug-resistant cells. | |||
TN6020 | 4-Hydroxycephalotaxine | ||
4-Hydroxycephalotaxine is a natural product from Cephalotaxus fortunei. | |||
TN6271 |
11β,13-Dihydrotaraxinic acid β-D-glucopyranosyl ester
|
||
11β,13-Dihydrotaraxinic acid β-D-glucopyranosyl ester 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6271,CAS号为 75911-16-9。 | |||
TN5378 |
Axinysone A
(-)-Axinysone A |
||
Axinysone A 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5378,CAS号为 1114491-57-4。 | |||
TN3787 | Decinnamoyltaxinine J | Others | Others |
Decinnamoyltaxinine J is a natural product from Taxus brevifolia Nutt. | |||
TN5112 | Taxin B | Others | Others |
Taxin B has toxic effects. | |||
TN6236 | Taraxinic acid | ||
Taraxinic acid 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6236,CAS号为 75911-33-0。 | |||
TN5116 | Taxinine M | Others | Others |
Taxinine M is a natural product from Chinese yew Taxus chinensis. | |||
TN3222 | 7-Deacetoxytaxinine J | Others | Others |
7-Deacetoxytaxinine J 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3222,CAS号为 18457-45-9。 | |||
T75625 | Axinelline A | ||
Axinelline A 是一种有效的 COX 抑制剂,对 COX-2和 COX-1的IC50分别为 2.22 μΜ 和 8.89 μM。Axinelline A 显示抗炎活性。 | |||
TN2752 |
2-Deacetoxytaxinine J
|
Others | Others |
2-Deacetoxytaxinine J shows significant in vitro activity against breast cancer cell line at a concentration of 20 microM and 10 microM in MCF-7 and MDA-MB-231 respectively. | |||
TN6254 |
11β,13-Dihydrotaraxinic acid
|
||
11β,13-Dihydrotaraxinic acid 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6254,CAS号为 1274668-83-5。 | |||
T81020 |
Tenaxin I
|
||
Tenaxin I,一种从黄芩提取物中鉴定出的成分,具有神经氨酸酶抑制活性。 | |||
TN6269 |
Taraxinic acid β-D-glucopyranosyl ester
|
||
Taraxinic acid β-D-glucopyranosyl ester 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6269,CAS号为 75911-14-7。 | |||
TN2742 |
2,7-Dideacetoxytaxinine J
|
Others | Others |
2,7-Dideacetoxytaxinine J 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2742,CAS号为 115810-14-5。 | |||
TN5115 |
Taxinine J
|
Others | Others |
Taxinine J possesses inhibitory activity on heptoma cell in vitro. | |||
TN4567 |
Minaxin C
|
Others | Others |
Minaxin C is a natural product from Caesalpinia minax HANCE. | |||
TN5376 |
Axinysone B
(-)-Axinysone B |
||
Axinysone B is a natiral product from the metabolites of the mushroom Anthracophyllum sp. BCC18695. | |||
TN2751 | 2-Deacetoxydecinnamoyltaxinine J | Others | Others |
2-Deacetoxydecinnamoyltaxinine J is a natural product from Taxus cuspidta Sibe et Zucc. | |||
TN3823 |
Demethylcephalotaxinone
|
Others | Others |
Demethylcephalotaxinone is a natural product from Cephalotaxus fortunei. | |||
TN3341 |
Acetylcephalotaxine
|
Others | Others |
Acetylcephalotaxine是一种天然产物,属于三尖杉科三尖杉属,其产品编号为 TN3341,CAS号为 24274-60-0。Acetylcephalotaxine可用作对照参考。 | |||
TN5569 |
2-Deacetoxytaxinine B
|
||
2-Deacetoxytaxinine B is a strongly inhibitor against U46619-induced aggregation, it shows strong inhibitory effects against arachidonic acid (AA)-induced aggregation. |