129
48
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11254 |
F-1
|
ROS; ALK; ROS Kinase | Angiogenesis; Immunology/Inflammation; Tyrosine Kinase/Adaptors |
F-1 是 ALK 和 ROS1 的双重抑制剂,抑制 ALK 的磷酸化及下游通路,可作用于对 ALKWT (IC50:2.1 nM),ROS1WT (IC50:2.3 nM),ALKL1196M (IC50:1.3 nM) 和 ALKG1202R (IC50:3.9 nM)。 | |||
T30665 |
C.I. Direct Red 1, disodium salt
Japanol Fast Red 1,COLUMBIA FAST RED F,Chrome Fast Red F,Neonyl Red 2B,Enianil Fast Red F |
||
C.I. Direct Red 1, disodium salt is a dye. | |||
T34652 |
SK&F 39728-A
SK&F39728-A,SK&F 1-39728,SK&F-39728-A,Skf 39728-A |
||
SK&F 39728-A is a bioactive chemical. | |||
T19840 |
GSK-F1
PI4KA inhibitor-F1 |
PI4K | PI3K/Akt/mTOR signaling |
GSK-F1 (PI4KA inhibitor-F1) 是一种新型强效 PI4KA 抑制剂。 | |||
T19688 |
Lodenosine
FddA,3'-dideoxyarabinosyladenine,Fddl,2'-F-dd-ara-A,2'-Fluoro-2',DDG-1 |
||
Lodenosine is an inhibitor of RNA-directed DNA polymerase, and potentially for the treatment of HIV. | |||
T19618 |
(R)-(-)-JQ1 Enantiomer
(R)-(-)2-(4-(4-氯苯基)-2,3,9-三甲基-6H-噻吩并[3,2-F][1,2,4]三唑并[4,3-A][1,4]二氮杂环庚烷-6-基)乙酸叔丁酯 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
(R)-(-)-JQ1 Enantiomer 是 (+)-JQ1 的立体异构体。 (+)-JQ1 是一种 BET 溴结构域抑制剂,对BRD4(1/2)的IC50 为 77 和 33 nM。 | |||
TP2476 |
Tnrnflrfamide
Thr-asn-arg-asn-phe-leu-arg-phe-NH2,Peptide F(1), lobster,F1 Peptide, lobster,Lobster peptide F1 |
||
Tnrnflrfamide is a SCP (small cardioactive peptide)-like peptide found in lobster neurons; exhibits FMRFamide-like immunoreactivity. | |||
T65682 | 11-(1-Piperazinyl)-dibenzo[b,f][1,4]thiazepine dihydrochloride | ||
11-(1-Piperazinyl)-dibenzo[b,f][1,4]thiazepine dihydrochloride 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 T65682,CAS号为 111974-74-4。 | |||
T65991 | (S)-4-Phenoxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine | ||
(S)-4-Phenoxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 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 T65991。 | |||
T65992 | (R)-4-Phenoxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine | ||
(R)-4-Phenoxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 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 T65992。 | |||
T64437 | 5-(11bR)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl-5H-dibenz[b,f]azepine | ||
5-(11bR)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl-5H-dibenz[b,f]azepine 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 T64437。 | |||
T64639 | (11AS)-5-(4,5,6,7-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-yl)-5H-dibenzo[b,f]azepine | ||
(11AS)-5-(4,5,6,7-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-yl)-5H-dibenzo[b,f]azepine 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 T64639。 | |||
T64513 |
(11aR)-5-(4,5,6,7-Tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-yl)-5H-dibenzo[b,f]azepine
|
||
(11aR)-5-(4,5,6,7-Tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-yl)-5H-dibenzo[b,f]azepine 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 T64513。 | |||
T67388 | N-(1-((6aR,8R,9aR)-9-Cyano-9-hydroxy-2,2,4,4-tetraisopropyltetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide | ||
N-(1-((6aR,8R,9aR)-9-Cyano-9-hydroxy-2,2,4,4-tetraisopropyltetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide 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 T67388。 | |||
T17877 |
VH032-cyclopropane-F
VHL ligand 3,E3 ligase Ligand 19,Phenolic VH101 |
Others; Ligand for E3 Ligase | Others; PROTAC |
VH032-cyclopropane-F (Phenolic VH101) 是基于 VH032 的 VHL 配体。它能够利用 linker 与靶蛋白配体连接,得到 PROTAC 分子,如 PROTAC 1。PROTAC 1 是 SMARCA2 和 SMARCA4 的部分降解剂。 | |||
T62204 |
NR2F6 modulator-1
|
Others | Others |
NR2F6 modulator-1 是一种核受体亚族 2,F 组第 6 号成员 (NR2F6) 的有效调节剂。NR2F6 modulator-1 能够用于研究免疫调节和肿瘤干细胞活性的调节。 | |||
T15660 |
KHK-IN-1
KHK-IN-8,Ketohexokinase inhibitor 8 |
Others | Others |
KHK-IN-1 (KHK-IN-8) 是一种选择性的、细胞膜渗透性的己酮糖激酶 (KHK) 抑制剂 (IC50=12 nM; F=34%)。KHK-IN-1 抑制 HepG2 细胞裂解液中 F1P 生成,IC50为400 nM。KHK-IN-1 可用于研究糖尿病和肥胖症。 | |||
TP1926 |
WRW4 TFA(878557-55-2 free base)
WRW4 |
Others | Others |
WRW4 TFA (878557-55-2 free base) 是一种特异性的甲酰肽受体样 1 (FPRL1) 拮抗剂,抑制 WKYMVm 与 FPRL1 的结合,IC50 为 0.23 μM。 WRW4 通过 FPRL1 激动剂 MMK-1、淀粉样蛋白 beta42 (Abeta42) 肽和 F 肽特异性抑制细胞内钙的增加。 | |||
T4647 |
M2I-1
M2I 1 |
Others | Others |
M2I-1 是Mad2抑制剂,靶向的 Mad2 与 Cdc20 的结合,该结合是纺锤体装配检查点内必不可少的蛋白-蛋白相互作用。 | |||
T4603 |
PEO-IAA
2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid |
Others | Others |
PEO-IAA (2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid) 是一种生长素拮抗剂,是一种吲哚-3-乙酸拮抗剂,能够与转运抑制剂响应蛋白 1/生长素信号 F-box 蛋白 (TIR1/AFBs) 结合。 | |||
T36682 |
USP30 inhibitor 18
|
DUB | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination |
USP30 inhibitor 18 是有效的USP30选择性抑制剂,IC50为 0.02 μM。它增加蛋白质泛素化并加速线粒体自噬。 | |||
T38192 |
Unifiram
|
Others | Others |
Unifiram 是一种认知增强剂。 Unifiram 诱导大鼠海马 CA1 区场兴奋性突触后电位 (fEPSP) 幅度的持久增加 (EC50= 27 nM) 并增加大鼠大脑皮层中乙酰胆碱 (ACh) 的释放。 | |||
T34651 |
SK&F 108361
Skf-108361,SK&F-108361,Skf 108361,SK&F108361,Skf108361 |
||
SK&F 108361 is a symmetric diol that binds HIV-1 protease symmetrically. | |||
T80318 |
Temporin F
|
||
Temporin F是针对Legionella pneumophila具有抗菌活性的肽类化合物。 | |||
T76153 |
PNGase F
|
||
PNGase F 是一种糖苷酶,可催化寡糖中内部糖苷键的裂解。PNGase F 可从糖蛋白中去除几乎所有的 N-连接寡糖。 | |||
T61366 |
F-17
|
||
F-17 is a promising virulence factor inhibitor, displaying substantial inhibitory effects on biofilm formation, elastase activity, pyocyanin production, and swarming motility. Additionally, F-17 exhibits a strong binding affinity towards LasR and PqsR. Notably, F-17 does not exhibit any discernible cytotoxicity [1]. | |||
T81511 |
Peptide F, bovine
|
||
Peptide F, bovine,是源自牛大脑和肾上腺髓质的前脑啡肽F,与脑啡能系统的疼痛传导过程相关。 | |||
T74032 | Ara-F-NAD+ sodium | ||
Ara-F-NAD+ sodium 是一种 NAD+的 arabino 类似物。Ara-F-NAD+ sodium 是一种有效的、可逆的、缓慢结合的CD38NADase 抑制剂。 | |||
T61540 | F15845 | ||
F 15845 is a potent and persistent blocker of the sodium current. It possesses cardioprotective properties and exhibits both anti-ischemic activity and short- and long-term cardioprotection following myocardial infarction. Furthermore, F 15845 finds utility in the investigation of myocardial functional impairment [1]. | |||
T82290 |
Glycocin F
|
||
Glycocin F为一种具有针对乳杆菌活性的抗菌肽。 | |||
T73606 |
Bleomycin B4
|
||
Bleomycin B4 (Phleomycin F),一种具有抗肿瘤活性的抗生素,常用于癌症研究。 | |||
T75412 | Peptide-N-Glycosidase F (PNGaseF) | ||
Peptide-N-Glycosidase F (PNGaseF) 是一种天冬酰胺酰胺酶。Peptide-N-Glycosidase F 催化来自糖蛋白的高甘露糖、杂合和复杂寡糖的内层 GlcNAc 和天冬酰胺残基之间的 N-连接寡糖裂解。Peptide-N-Glycosidase F 可用于糖蛋白的结构和功能研究。 | |||
T76579 |
Di-aspartic acid
|
||
Di-aspartic acid (Aspartylaspartate) 可作为 P. gingivalis、P. intermedia、P. nigrescens 和 F. nucleatum 的生长底物。 | |||
T126464 |
Saucerneol F
|
||
Saucerneol F 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 T126464,CAS号为 1061273-57-1。 | |||
T123847 |
Hexanorcucurbitacin F
|
||
Hexanorcucurbitacin F 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 T123847,CAS号为 96253-53-1。 | |||
T76902 | Afelimomab | ||
Afelimomab (MAK 195F)为F(ab')2型单克隆抗体片段,针对肿瘤坏死因子抗体,应用于脓毒症研究。 | |||
T33446 |
MK-9470
MK 9470,MK9470 |
||
MK-9470 is a selective, high-affinity reverse agonist and is also a fluorine 18 labeled positron emission tomography (PET) radiotracer [(18) F]. The MK-9470 has been used to image cannabinoid receptor type 1 in healthy and ill human brains. | |||
T37002 |
7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate (ammonium salt)
|
||
7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate (SBD-F) is a thiol-reactive fluorogenic probe.1It has been used to quantify the levels of homocysteine, cysteine, and cysteamine in human plasma.2SBD-F displays excitation/emission maxima of 380/515 nm, respectively.1 1.Imai, K., Toyo’oka, T., and Watanabe, Y.A novel fluorogenic reagent for thiols: Ammonium 7-fluorobenzo-2-oxa-1,3-diazole-4-sulfonateAnal. Biochem.128(2)471-473(1983) 2.Ichinose, S., Nakamura, M., Maeda, M., et al.A validated HPLC-fluoresc... | |||
T18251 |
MAL-di-EG-Val-Cit-PAB-MMAF
|
Others | Others |
MAL-di-EG-Val-Cit-PAB-MMAF refers to a chemical compound that comprises the linker (MAL-di-EG-Val-Cit-PAB) and the potent blocker of tubulin polymerization (MMAF, Monomethyl auristatin F)[1]. | |||
T124590 | Cucurbitacin F | ||
Cucurbitacin F 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 T124590,CAS号为 5939-57-1。 | |||
T79883 |
9-Chloromethyl-10-hydroxy-11-F-Camptothecin
|
Topoisomerase | DNA Damage/DNA Repair |
9-Chloromethyl-10-Hydroxy-11-F-Camptothecin是一款喜树碱类衍生化合物,具有DNA拓扑异构酶I (Topo I)抑制活性,应用于癌症治疗的研究领域。 | |||
T35485 |
6-Prenylindole
|
||
6-Prenylindole is a bacterial metabolite that has been found in Streptomyces and has antifungal and antimalarial properties.1 It is active against A. brassicicola strain TP-F0423 and F. oxysporum f. sp. tulipae TU-4-2 (15 and 30 μg/disc in the paper disc assay), and also drug-resistant P. falciparum strain K1 (IC50 = 21 μg/ml).2 |1. Sasaki, T., Igarashi, Y., Ogawa, M., et al. Identification of 6-prenylindole as an antifungal metabolite of Streptomyces sp. TP-A0595 and synthesis and bioactivity o... | |||
T75357 |
DMTr-4'-F-U-CED-TBDMS phosphoramidite
|
||
DMTr-4'-F-U-CED-TBDMS phosphoramidite (DMTr-4'-F-uridine-CED-TBDMS phosphoramidite) 是一种用于标记寡核苷酸的染料试剂,可用于研究 RNA 疗法。DMTr-4'-F-U-CED-TBDMS phosphoramidite 代表了一种用于阐明 RNA 结构的广泛用途的探针。储存方式:避光。 | |||
T64496 | 7-Iodopyrrolo[2,1-f][1,2,4]triazin-4-amine | ||
7-Iodopyrrolo[2,1-f][1,2,4]triazin-4-amine 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 T64496,CAS号为 1770840-43-1。 | |||
T40752 |
Ibuprofen Impurity F
|
||
Ibuprofen Impurity F is a known impurity of Ibuprofen, which acts as an anti-inflammatory inhibitor that selectively targets both COX-1 and COX-2 enzymes. It exhibits inhibitory activity with IC50 values of 13 μM and 370 μM for COX-1 and COX-2, respectively. | |||
T65834 |
Fmoc-D-Phe(3-F)-OH
|
||
Fmoc-D-Phe(3-F)-OH 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 T65834,CAS号为 198545-72-1。 | |||
T79199 |
F-CRI1
|
STING | Immunology/Inflammation |
F-CRI1为高效STING激动剂,Kd值达40.62 nM。该化合物通过18F标记成为放射性探针,适用于肿瘤微环境中STING可视化的研究。 | |||
T64635 | 8-Phenyl-2,6-diethyl-BODIPY 505/515 | ||
2,8-Diethyl-5,5-difluoro-1,3,7,9-tetramethyl-10-phenyl-5H-4l4,5l4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinine 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 T64635。 | |||
T77027 | Gontivimab | ||
Gontivimab (ALX-0171; VR-465) 是一种有效的抗RSV 预融合 F 蛋白纳米抗体,KD 值为 0.113 nM。Gontivimab 显示出抗病毒活性。Gontivimab 可降低鼻腔和肺部的RSV 负荷。 | |||
T77005 | Felvizumab | ||
Felvizumab (SB 209763) 是一种人源化 IgG1κ 单克隆抗体,靶向RSVF 糖蛋白上的不同中和表位。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5S2139 |
Epimedin A1
朝藿定A1,Hexandraside F |
Others | Others |
Epimedin A1 (Hexandraside F) 是一种黄酮类化合物,从常用中药淫羊藿中提取得到。 | |||
T8716 |
physalin F
酸浆苦味素F,酸浆苦素 F |
Apoptosis | Apoptosis |
Physalin F 是一种分泌型甾体,诱导人外周血单个核细胞凋亡,降低人 T 淋巴细胞 1 型病毒感染后的自发增殖和细胞因子的产生,具有强烈抗炎和免疫调节作用。 | |||
T3401 |
Ginsenoside F1
人参皂苷 F1,20(S)-Ginsenoside F1 |
P450; Endogenous Metabolite | Metabolism |
Ginsenoside F1 (20(S)-Ginsenoside F1) 是一种 Ginsenoside Rg1 的酶促修饰衍生物,它竞争性抑制CYP3A4,对 CYP2D6 具有较弱的抑制作用。 | |||
T3920 |
Pseudoginsenoside F11
Ginsenoside A1,拟人参皂苷 F11,拟人参皂苷F11 |
Others; Endogenous Metabolite | Metabolism; Others |
Pseudoginsenoside F11 (Ginsenoside A1) 从人参根和叶中分离得到。PF11在一系列心血管和中枢神经系统疾病中具有广泛的保护作用。 | |||
TN2341 |
Cucurbitacin Q1
葫芦素F-25-乙酸酯,葫芦素Q1 |
Others | Others |
Cucurbitacin Q1 是一种天然的四环三萜,来源于Cucumis prophetarum。 | |||
TN6864 |
Prosaikogenin F
(2R,3R,4S,5R,6R)-2-{[(1S,2R,4S,5R,8R,9S,10R,13S,14R,17S,18R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-en-10-yl]oxy}-6-methyloxane-3,4,5-triol,前柴胡皂苷F |
Others | Others |
Prosaikogenin F ((2R,3R,4S,5R,6R)-2-{[(1S,2R,4S,5R,8R,9S,10R,13S,14R,17S,18R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-en-10-yl]oxy}-6-methyloxane-3,4,5-triol) 是一种单糖苷,具有溶血和抗癌特性。 | |||
TN2119 |
Pulsatilla saponin H
白头翁属皂苷H,白头翁皂苷 H,3-O-Β-D-葡萄糖( 1→4)-[ A -L-鼠李糖(1→2)]- A-L-阿拉伯糖 常春藤配基- 28-O-鼠李糖(1→4)葡萄糖(1→6)葡萄糖苷 |
Others | Others |
Pulsatilla saponin H 是一种从 Pulsatilla koreana 的根中分离出来的天然产物。 | |||
TN4161 |
Goshonoside F1
|
||
Goshonoside F1是半糯米品种水稻的脂质代谢产物,可被当作培育优良水稻的一个指标。 | |||
TN1942 |
Momordicoside F1
苦瓜皂苷 F1 |
Others | Others |
Momordicoside F1 may have antiproliferative activities against MCF-7, WiDr, HEp-2, and Doay human tumor cell lines. | |||
TN1080 |
Kaji-ichigoside F1
蔷薇苷 |
||
Kaji-ichigoside F1 shows antiinflammatory/antinociceptive action in acetic acid-induced writhing and hot plate testing and in a carrageenan-induced paw edema model in mice and rats. Kaji-ichigoside F1 exhibits in vivo hepatoprotective effects, it inhibite | |||
TN1989 |
Niga-ichigoside F1
苦莓苷F1 |
Others; Nrf2 | Immunology/Inflammation; Others |
Niga-ichigoside F1(NI) has anti-inflammatory, gastroprotective ,antinociceptive, and cytotoxic effects. | |||
TN6859 |
Saikogenin F
(1S,2S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-ene-2,10-diol |
Others | Others |
Saikogenin F ((1S,2S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-ene-2,10-diol) 是一种具有抗癌活性的天然产物。 | |||
TMA2270 |
Alisol F 24-acetate
|
P-gp | Membrane transporter/Ion channel; Neuroscience |
Alisol F 24-acetate 是一种从 Alisma plantago-aquatica Linn [1] 中分离出来的天然产物。 Alisol F 24 Acetate 通过抑制 P-糖蛋白介导的药物流出来增强 MCF-7/DOX 细胞的化学敏感性和凋亡。 | |||
T2S0491 |
Isoeugenol acetate
乙酸异丁香酚酯,Isoeugenyl acetate,Acetisoeugenol,Acetylisoeugenol,乙酸异丁香酚酯,乙酰基异丁香酚;2-甲氧基-4-丙烯基苯基乙酸酯 |
AChE; Antifungal | Microbiology/Virology; Neuroscience |
Isoeugenol acetate (Acetylisoeugenol) 是肉豆蔻,丁香和肉桂的精油成分,对某些代谢酶如乙酰胆碱酯酶,能够抑制α-糖苷酶和 α-淀粉酶。它用于医疗和化妆品工业,具有抗氧化,抗癌,抗菌和抗炎作用。 | |||
T5S1054 |
Wilforgine
雷公藤晋碱,雷公藤精碱 |
Others | Others |
Wilforgine 是一种具有生物活性的倍半萜烯生物碱,存在于Tripterygium wilfordiiHook. F 中。它能诱导分离出丝状体幼虫肌肉的微结构和超微结构变化,其作用部位被认为是肌肉系统中的钙受体或通道。 | |||
T4S0498 |
Glaucocalyxin A
蓝萼甲素,Wangzaozin B,Leukamenin F |
Apoptosis; Akt; Caspase; PI3K | Apoptosis; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Glaucocalyxin A (Leukamenin F) 是来自日本黑纹病菌的一种对映型月桂基二萜,具有抗肿瘤作用。它通过调节PI3K/Akt 信号通路抑制 GLI1 的核易位,诱导骨肉瘤凋亡。 | |||
T36914 |
2-Hydroxyanthraquinone
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Others | Others |
2-Hydroxyanthraquinone 是一种天然产物,显示出抗肿瘤和免疫抑制活性。 | |||
T3S0027 |
Picropodophyllotoxin
AXL 1717,Picropodophyllin,苦鬼臼毒素 |
IGF-1R | Tyrosine Kinase/Adaptors |
Picropodophyllotoxin (AXL 1717) 是一种环木脂素生物碱,存在于五月树(Podophyllum peltatum) 中,是一种具有潜在抗肿瘤活性的胰岛素样生长因子 1 受体 (IGF1R) 的小分子抑制剂。它特异性抑制 IGF1R 的活性并下调细胞表达,而不干扰其他生长因子受体的活性,例如胰岛素受体、表皮生长因子、血小板衍生生长因子、成纤维细胞生长因子和肥大/干细胞生长因子 (KIT) )。该药剂在抑制肿瘤细胞增殖和诱导肿瘤细胞凋亡方面显示出有效的活性。 IGF1R 是一种在多种人类癌症中过度表达的受体酪氨酸激酶,在多种癌细胞的生长和存活中起关键作用。 | |||
T75654 | F-14329 | ||
F-14329 是一种四元酸真菌代谢物。 | |||
T80864 | Virgaureagenin F | ||
Virgaureagenin F, 一种从Rhizoma bolbostemmae中提取的皂苷。 | |||
T83216 |
Abiesadine F
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Abiesadine F为从Abies georgei Orr分离出的一种二萜化合物。 | |||
T83107 |
Anhuienside F
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Anhuienside F,一种从Anemone vitifolia Buch.-Ham根部提取的天然化合物。 | |||
T82399 |
Fipsomin
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Fipsomin为从F. nipponica果实中提取的天然化合物。 | |||
TN4411 |
Lappaol F
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CDK; P-gp; JNK | Cell Cycle/Checkpoint; MAPK; Membrane transporter/Ion channel; Neuroscience |
1. Lappaol F has antioxidant and antiaging properties, it may promote the C. elegans longevity and stress resistance through a JNK-1-DAF-16 cascade. <br/> 2. Lappaol F has potential chemosensitizing activity, it may be candidates for developing novel adju | |||
T79992 |
Sarglaroids F
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Caspase | Apoptosis; Proteases/Proteasome |
Sarglaroids F(化合物6)为从草珊瑚根部提取的抗炎剂,影响K+外排并降低Caspase-1(P20)水平以抑制LPS/ATP诱导的IL-1β释放,对RAW264.7细胞无细胞毒性。 | |||
T81093 | Sterebin F | ||
Sterebin F, 一种甾类化合物,来源于Stevia rebaudiana叶的分离提取,表现出降血糖的活性。 | |||
T82738 |
Chisocheton compound F
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Chisocheton compound F,一种从Melia toosendan茎皮中分离的天然产物。 | |||
TMA0593 | Broussoflavonol F | Tyrosinase | Proteases/Proteasome |
Broussoflavonol F has antiplatelet effect, is partially due to an inhibitory effect on cyclooxygenase, can inhibit arachidonic acid (AA)-induced platelet aggregation. Broussoflavonol F shows inhibitory activities on mushroom tyrosinase. Broussoflavonol F | |||
T83565 | (2E)-Leocarpinolide F | ||
(2E)-Leocarpinolide F(化合物20),为从Sigesbeckia orientalis中提取的香叶鹤型倍半萜。 | |||
TN6249 | (+)-Isoampelopsin F | ||
(+)-Isoampelopsin F 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 TN6249,CAS号为 354553-38-1。 | |||
TN5988 |
16,25-Di-O-acetylcucurbitacin F
16,25-O-Diacetyl-cucurbitane F,Cucurbitacin F 16,25-diacetate |
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16,25-Di-O-acetylcucurbitacin F 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 TN5988,CAS号为 2062685-10-1。 | |||
T83108 |
Anhuienoside B
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Anhuienoside B为从C. anhuiensis K. F. Wu鲜叶中提取的天然产物,能应对CuCl2诱导的非生物胁迫。 | |||
T80941 | Triptonoterpene Me ether | ||
Triptonoterpene Me ether(compound 5)为一种从中药雷公藤(Tripterygium wilfordii Hook. f.)分离出的松香烷型二萜类化合物。 | |||
T81941 | Leocarpinolide F | ||
Leocarpinolide F,一天然提取自Siegesbeckia orientalis的类倍半萜烯。 | |||
T82338 |
Ganoapplanoid F
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Ganoapplanoid F,一种三萜类化合物,源自Ganoderma applanatum,具有抑制脂肪细胞脂质积累的功能,适用于肥胖研究领域。 | |||
TN4977 | Scutebata F | Others | Others |
Scutebata F 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 TN4977,CAS号为 1207181-62-1。 | |||
T79937 |
Mortatarin F
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Glucosidase | Metabolism |
Mortatarin F (Compound 1) 是一种具有戊烯基化类黄酮结构的葡萄糖苷酶抑制剂,其IC50值为8.7 μΜ。该化合物可从桑叶中提取,并应用于研究降低血糖效果。 | |||
T82067 |
Inonotusol F
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Inonotusol F, 一种三萜化合物,可在Inonotus obliquus中分离出。该化合物对D-半乳糖胺诱导的WB-F344细胞损伤显示出保肝效应。 | |||
T80002 |
Wulfenioidin F
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Virus Protease | Microbiology/Virology |
Wulfenioidin F是从Orthosiphon wulfenioides全草分离的二萜类化合物。该化合物对抗寨卡病毒(ZIKV)活性显著,其半数有效浓度(EC50)为8.07 μM。Wulfenioidin F的抗病毒机制通过抑制ZIKV包膜(E)蛋白的表达,从而干扰病毒复制。 | |||
T82459 |
Epicornuin F
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Epicornuin F,一种源自Epimedium brevicornu叶片的异戊二烯黄酮化合物,展现了对HepG2细胞线的显著细胞毒性,IC50为33.4 μM,适用于癌症研究领域。 | |||
T82986 |
Apigenin triacetate
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Apigenin triacetate, 作为禾谷镰刀菌的代谢产物,其含量可通过壳聚糖处理以实现下调。该化合物系由芹菜素派生。 | |||
T83479 |
1,2,6,7,8,9-Hexahydro-1,6,6-trimethyl-3,11-dioxanaphth[2,1-e]azulene-10,12-dione
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1,2,6,7,8,9-Hexahydro-1,6,6-trimethyl-3,11-dioxanaphth[2,1-e]azulene-10,12-dione 是一种从丹参酮 (Salvia miltiorrhiza f. alba) 中提取的化学物质,具有二氢异丹参酮结构,显示出细胞毒性和抗肿瘤的活性。 | |||
TMA1012 |
Ganoderiol F
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Androgen Receptor; HIV Protease; Autophagy | Autophagy; Endocrinology/Hormones; Microbiology/Virology; Proteases/Proteasome |
Ganoderiol F has anti-inflammatory, cytotoxic and anti-HIV activity, it inhibits activity of topoisomerases in vitro, and it inhibits human immunodeficiency virus-1 protease with IC(50) values of 20-40 microM. It induced HO-1 expression, activation of the mitogen-activated protein kinase EKR and up-regulation of cyclin-dependent kinase inhibitor p16 and suppressed lipopolysaccharide (LPS)-induced nitric oxide (NO) production. | |||
T81676 |
NG-012
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NG-012为一种神经生长因子(NGF)增强剂,来源于Penicillium verruculosum F-4542的培养液。该化合物能在大鼠嗜铬细胞瘤细胞系(PC12)中提升NGF引导的神经突生长效应。 | |||
T81531 |
Pedunculosumoside F
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Pedunculosumoside F,一种从Ophioglossum pedunculosum分离得到的同型黄酮苷,对HepG2 2.2.15细胞表现出细胞毒性,其CC50值为56.7 μM,但缺乏抗HBV活性。然而,其类似物能够抑制HBV感染的HepG2 2.2.15细胞中HBsAg的分泌。 | |||
T75540 |
Ipomoeassin F
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Ipomoeassin F 是一种高效且具有选择性的内质网(ER)蛋白转位抑制剂,它通过作用于ER膜上的Sec61复合物(Sec61α)的成孔亚基来实现其功能。此化合物能特异性抑制SARS-CoV-2蛋白在ER膜上的转位,同时阻碍分泌蛋白和I型跨膜蛋白(TMP)的ER转运,但对III型TMP的转运不产生影响。 | |||
T36000 |
3-Hydroxyterphenyllin
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3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,3,4 It has a 96% scavenging effect on 2,2-diphenyl-1-picrylhydrazyl radicals when used at a concentration of 100 μg/ml.2 3-Hydroxyterphenyllin inhibits the growth of HeLa cervical, A549 lung, and HepG2 liver cancer cells (IC50s = 23, 36, and 32 μM, respectively), as well as methi... | |||
T36954 |
Nemorosone
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Nemorosone is a polycyclic polyprenylated acylphloroglucinol (PPAP) originally isolated from C. rosea that has antiproliferative properties.1 Nemorosone inhibits growth of NB69, Kelly, SK-N-AS, and LAN-1 neuroblastoma cells (IC50s = 3.1-6.3 μM), including several drug-resistant clones, but not MRC-5 human embryonic fibroblasts (IC50 = >40 μM).2 It increases DNA fragmentation in LAN-1 cells in a dose-dependent manner, and decreases N-Myc protein levels and phosphorylation of ERK1/2 by MEK1/2. Nem... |