144
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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11593 |
I-OMe-Tyrphostin AG 538
I-OMe-AG 538 |
IGF-1R; PI3K | PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
I-OMe-Tyrphostin AG 538是一种特异性 IGF-1R 抑制剂和 PI5P4Kα的 ATP 竞争性抑制剂(IC50:1 µM)。I-OMe-Tyrphostin AG 538可抑制 IGF-1R 介导的信号传导,并对营养缺乏的 PANC1细胞具有优先细胞毒性。 | |||
T7649 |
Tyrphostin A1
AG9,(4-甲氧基苄烯)丙二腈,Tyrphostin 1 |
EGFR; Interleukin | Angiogenesis; Immunology/Inflammation; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin A1 (Tyrphostin 1) 对巨噬细胞培养中CD40L 刺激的IL-12产生和抗原诱导的Th1细胞生成具有抑制作用。 | |||
T67707 |
Tyrphostin AG 538
AG 538 |
IGF-1R | Tyrosine Kinase/Adaptors |
Tyrphostin AG 538 是一种查尔酮化合物,是一种IGF-1受体激酶抑制剂(IC₅0 :为400 nM),具有有效性、细胞渗透性、可逆性和竞争性。 | |||
T6711 |
Tyrphostin AG1296
Tyrphostin AG 1296,AG 1296 |
Apoptosis; FGFR; FLT; PDGFR; c-Kit | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
Tyrphostin AG1296 (Tyrphostin AG 1296) 抑制人PDGF α和β受体以及相关干细胞因子受体的信号传导,是一种选择性血小板衍生生长因子受体抑制剂,IC50值为 0.8 μM。 | |||
T22450 |
Tyrphostin B44, (+) enantiomer
酪氨酸磷酸化抑制剂AG 835 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin B44, (+) enantiomer 是一种表皮生长因子受体 (EGFR) 激酶抑制剂,IC50 为 0.86 μM,活性低于 (-) 对映体。 | |||
T7101 |
Tyrphostin AG30
Tyrphostin AG30(AG30),酪氨酸磷酸化抑制剂 AG 30 |
EGFR; Tyrosine Kinases | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin AG30 (AG30) 是一种有效的蛋白质酪氨酸激酶 (PTK) 抑制剂,选择性地抑制 c-ErbB 的自我更新诱导,并能抑制原发性红细胞 c-ErbB 激活 STAT5。 | |||
T8534 |
Tyrphostin AG 112
|
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin AG 112 是一种EGFR 磷酸化抑制剂。 | |||
T6712 |
Tyrphostin AG 879
AG 879 |
Apoptosis; EGFR; Trk receptor; HER; PDGFR | Angiogenesis; Apoptosis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin AG 879 (AG 879) 是一种抑制TrKA 磷酸化的酪氨酸激酶抑制剂,IC50为 10 μM。它还是一种选择性ErbB2酪氨酸激酶抑制剂,IC50为 1 μM,具有抗癌活性。 | |||
T34973 |
Tyrphostin 8
4-Hydroxybenzylidenemalononitrile |
EGFR; GTPase | Angiogenesis; GPCR/G Protein; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin 8(4-Hydroxybenzylidenemalononitrile) 是一种有效的 GTP 酶抑制剂,对 EGFR 激酶有抑制作用, IC50 值为 560 μM。Tyrphostin 8 可抑制蛋白丝氨酸/苏氨酸钙调磷酸酶 (IC50=21 μM),增强 Caco-2 细胞中转铁蛋白受体介导的转吞作用,并增加口服胰岛素 - 转铁蛋白的降血糖作用。 | |||
T2063 |
Tyrphostin 23
RG-50810,TX 825,Tyrphostin A23,AG18 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin 23 (AG18) 是一种EGFR 抑制剂,IC50值为35 μM。 | |||
T13238 |
Tyrphostin AG1433
SU1433,AG1433 |
VEGFR; PDGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Tyrphostin AG1433 (AG1433) 是选择性的PDGFRβ和VEGFR-2 (Flk-1/KDR)抑制剂,IC50分别为 5.0 μM 和 9.3 μM。Tyrphostin AG1433有防止血管形成的活性。 | |||
T4528 |
Tyrphostin AG 528
Tyrphostin B66,AG 528 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin AG 528 (Tyrphostin B66) 是一种蛋白酪氨酸激酶抑制剂,对表皮生长因子受体 (EGFR) 的IC50为 4.9 μM,对ErbB2的IC50为 2.1 μM,具有抗癌作用。 | |||
T22553 |
Adaphostin
1-Adamantyl 4-((2,5-Dihydroxybenzyl)Amino)Benzoate,NSC 680410 |
Bcr-Abl | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
Adaphostin (NSC-680410) 是 AG957 金刚烷酯,是一种 p210bcr/abl 抑制剂,可诱导 T 淋巴细胞白血病细胞系凋亡。它增加了 CLL B 细胞内活性氧的水平,对慢性和急性髓系白血病细胞具有显著的选择性活性。 | |||
T21622 |
Tyrphostin A25
AG-82,Tyrphostin AG 82,RG-50875 |
EGFR; GPR | Angiogenesis; Endocrinology/Hormones; GPCR/G Protein; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin A25 (Tyrphostin AG 82)是一种特异性的EGFR 酪氨酸激酶抑制剂和GPR35激动剂,对GPR35的IC50值为 0.94 μM,对GPR35的EC50值为 5.3 μM。 | |||
T2479 |
Tyrphostin A9
Malonoben,Tyrphostin 9,SF 6847,AG 17,RG-50872 |
EGFR; VEGFR; Influenza Virus; PDGFR | Angiogenesis; JAK/STAT signaling; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Tyrphostin A9 (SF 6847) 是一种线粒体分裂诱导剂,是 PDGFR 抑制剂,具有抗流感病毒的活性。 | |||
T29007 |
Trichostatin A S-isomer
(-)-Trichostatin A |
||
Trichostatin A S-isomer is the s-isomer of Trichostatin A. Trichostatin A is a histone deacetylase inhibitors (HDIs or HDACIs) that have a broad spectrum of epigenetic activities. Trichostatin A inhibits HDACs 1, 3, 4, 6 and 10 with IC50 values around 20 | |||
T77934 |
PhosTAC7
|
PROTACs | PROTAC |
PhosTAC7类似于PROTACs通过诱导三元复合物的作用机制,其主要作用是招募Ser/Thr磷酸酶至磷酸化底物,从而介导目标蛋白的去磷酸化。 | |||
T35825 |
Trichostatin C
|
||
Trichostatin C is a glycosylated derivative of trichostatin A , the antifungal antibiotic that reversibly inhibits histone deacetylase. Trichostatin C is reported to be the first example of a glucopyranosyl hydroxamate identified in nature. It has been shown to induce the differentiation of a mouse erythroleukemia cell line and to increase histone H4 acetylation in B cells, though at higher concentrations than trichostatin A. | |||
T71135 |
Calphostin I
|
||
Calphostin I is isolated from the fungus Cladosporium cladosporioides and is an inhibitor of protein kinase C (PKC). | |||
T24910 |
Tyrphostin A46
Tyrphostin A-46,Tyrphostin A 46 |
||
Tyrphostin A46 is an antagonist of the epidermal growth factor-urogastrone receptor. | |||
T24909 |
Tyrphostin 51
Tyrphostin A51,Tyrphostin A-51,Tyrphostin A 51 |
||
Tyrphostin 51 is an effective inhibitor of EGFR kinase. | |||
T24911 |
Tyrphostin AG 1112
Tyrphostin AG-1112,Tyrphostin AG1112 |
||
Tyrphostin AG 1112 is a Bcr-Abl kinase blocker. It can activate the terminal differentiation of K562 cells and the purging of Ph+ cells. | |||
T71238 |
Calphostin A
|
||
Calphostin A is isolated from the fungus Cladosporium cladosporioides and is an inhibitor of protein kinase C (PKC). | |||
T70232 | 3,4-Dephostatin | ||
3,4-Dephostatin is an inhibitor of the interactions of CFTR-associated ligand (CAL) and PSD-95/Dlg1/ZO-1 (PDZ) domain. | |||
T25056 | Alphostatin | ||
Alphostatin is an alkaline phosphatase inhibitor isolated from Bacillus megaterium. | |||
T31439 |
Didesacetylphyllanthostatin 3
Ddapt3,Ddapt 3,Ddapt-3 |
||
Didesacetylphyllanthostatin 3 is a biochemical. | |||
T27105 | Cyclophostin | ||
Cyclophostin is an irreversible inhibitor of acetylcholinesterase (AChE). | |||
T24912 |
Tyrphostin AG 568
Tyrphostin AG-568,Tyrphostin AG568 |
||
Tyrphostin AG 568 promotes Tyrphostin-induced inhibition of p210bcr-abl tyrosine kinase activity. It also induces K562 to differentiate. | |||
T22620 |
Calphostin C
|
Others | Others |
Calphostin C is a protein kinase C inhibitor. | |||
T28408 |
Phosphostim Sodium
IPH1101,Phosphostim,IPH 1101,IPH-1101 |
||
Phosphostim, a gamma9deta2 T lymphocytes agonist, is used potentially for the treatment of renal cell carcinoma, HCV infection. | |||
T24908 |
Tyrphostin 47
AG213,AG-213 AG 213 |
||
Tyrphostin 47 inhibits the protein-tyrosine kinase activity of EGF-R. | |||
T69658 | Ethyl-3,4-dephostatin | ||
Ethyl-3,4-dephostatin is a novel inhibitor of the interactions of CFTR-associated ligand and PSD-95/Dlg1/ZO-1 domain. | |||
T68822 |
Tyrphostin AG17
|
||
Tyrphostin AG17 is a biochemical that promotes adipocyte apoptosis in vivo and is an effective modulator of adipocyte differentiation and WAT hypertrophy in vitro and in vivo. It is thought to possibly be useful as a pharmacological obesity treatment. It is a tyrosine kinase antagonist that has also been found to inhibit tumor cell growth. | |||
T70392 |
Tyrphostin AG-808
|
||
Tyrphostin AG-808 is a 15-human lipoxygenase inhibitor. | |||
T71132 |
Calphostin D
|
||
Calphostin D is isolated from the fungus Cladosporium cladosporioides and is an inhibitor of protein kinase C (PKC). | |||
T71136 |
Calphostin B
|
||
Calphostin B is isolated from the fungus Cladosporium cladosporioides and is an inhibitor of protein kinase C (PKC). | |||
T25549 |
JCP174
JCP 174,JCP-174 |
Serine Protease | Proteases/Proteasome |
JCP174是一种去棕榈酰化酶抑制剂,可通过靶向 TgPPT1增强弓形虫的宿主细胞侵袭。 | |||
T16914 |
SP187
UV4,MON-DNJ |
Others; Virus Protease; Influenza Virus | Microbiology/Virology; Others |
SP187 (MON-DNJ) 是一种靶向作用于宿主的亚氨基糖。它具有抗丝状病毒感染活性。SP187可用于治疗抗流感和登革热病毒。 | |||
TP1741L |
Histatin 5 acetate
Histatin 5 acetate (115966-68-2 Free base) |
MMP | Proteases/Proteasome |
Histatin 5 acetate 抑制宿主基质金属蛋白酶 MMP-2 和 MMP-9 的活性,IC50 分别为 0.57 和 0.25 μM。 | |||
T9293 |
SSAA09E3
|
SARS-CoV | Microbiology/Virology |
SSAA09E3 是一种新型 SARS-CoV 复制抑制剂,通过阻止病毒膜与宿主细胞膜融合而起作用。 | |||
T7669 |
RPW-24
|
Antibacterial | Microbiology/Virology |
RPW-24 刺激线虫的宿主免疫反应,保护秀丽隐杆线虫免受细菌感染。它具有抗菌活性。 | |||
T9957 |
LASV inhibitor 3.3
|
Virus Protease | Microbiology/Virology |
LASV inhibitor 3.3 是一种针对溶酶体相关膜蛋白 1 (LAMP1) 的拉沙热病毒 (LASV) 抑制剂,LAMP1 是一种在感染期间与 LASV 糖蛋白 (GP) 结合的宿主因子。 | |||
T10009 |
JAK3-IN-7
|
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
JAK3-IN-7 是一种有效的选择性 JAK3 抑制剂(IC50<0.01 μM),可用于治疗器官移植中的排斥反应、器官移植后的移植物抗宿主反应、自身免疫性疾病、过敏性疾病和慢性骨髓增生性疾病。 | |||
T4982 |
Benznidazol
苄哒唑,苄硝唑,Radanil,Benznidazole,Ro 71051,Ro 07-1051 |
Antibiotic; Parasite | Microbiology/Virology |
Benznidazol (Benznidazole) 是一种抗寄生虫药物,对哥伦比亚 T. cruzi 菌株的 IC50值为 20.35 μM,有潜力研究美洲锥虫病。 | |||
T1486 |
Oseltamivir phosphate
GS 4104,磷酸奥司他韦 |
Influenza Virus | Microbiology/Virology |
Oseltamivir phosphate (GS 4104) 是一种神经氨酸酶抑制剂,可研究流感。 | |||
T8502 |
N-(1-benzyl-4-piperidyl)adamantane-1-carboxamide
|
Influenza Virus | Microbiology/Virology |
N-(1-benzyl-4-piperidyl)adamantane-1-carboxamide 通过与表面糖蛋白结合抑制埃博拉病毒进入宿主细胞,该化合物抑制埃博拉病毒,EC50 为 3.9 μM。 | |||
T16702 |
QL47
|
Virus Protease; BTK | Angiogenesis; Microbiology/Virology; Tyrosine Kinase/Adaptors |
QL47 是一种宿主靶向的小分子抗病毒剂,具有抗病毒活性,对登革热病毒和其他 RNA 病毒有抑制作用。QL47 可作为病毒翻译的抑制抑制剂和 BTK 的共价抑制剂,可用于研究淋巴瘤。 | |||
T21546 |
NG,NG-dimethyl-L-Arginine dihydrochloride
|
NO Synthase | Immunology/Inflammation |
NG,NG-dimethyl-L-Arginine dihydrochloride 是一种内源性一氧化氮合酶抑制剂。由 L-精氨酸合成的一氧化氮 (NO) 有助于调节血压和宿主防御。 | |||
T67753 |
Trifluoromethyl-tubercidin
|
Influenza Virus | Microbiology/Virology |
Trifluoromethyl-tubercidin (TFMT)可抑制宿主Mtr1并抑制病毒复制。TFMT 通过其S-adenosyl-l-methionine 结合袋相互作用抑制Mtr1,限制流感病毒复制。TFMT 能有效抑制病毒在小鼠体内的复制,毒性很小。 | |||
T0104 |
Umifenovir hydrochloride
盐酸阿比朵尔,Arbidol hydrochloride,Arbidol HCl,盐酸阿比多尔 |
SARS-CoV; Influenza Virus | Microbiology/Virology |
Umifenovir hydrochloride (Arbidol HCl) 是一种口服有效的广谱抗病毒药物,对多种包膜和非包膜病毒均有活性。它被用作抗流感病毒剂,可通过阻断病毒与宿主细胞膜的融合来抑制包膜病毒的细胞侵袭。它是一种 SARS-CoV-2 抑制剂,具有抗炎活性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN2331 |
Eleutheroside B1
刺五加苷B1 |
Influenza Virus | Microbiology/Virology |
Eleutheroside B1是具有广谱抗人流感病毒的一种香豆素。它抑制多种趋化因子基因和流感病毒核蛋白基因的 mRNA 表达。它具有抗病毒、抗流感和抗炎活性,且细胞毒性小。 | |||
T15720 |
Lathosterol
|
Endogenous Metabolite | Metabolism |
Lathosterol 是胆固醇样分子,其血清浓度是全身胆固醇合成的指标。 | |||
T6270 |
Trichostatin A
曲古柳菌素A,曲古抑菌素A,TSA |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Trichostatin A (TSA) 属于二烯异羟肟酸类的天然衍生物。Trichostatin A 是一种组蛋白去乙酰化酶抑制剂 (IC50=1.8 nM),具有可逆性和特异性。Trichostatin A 导致核心组蛋白过度乙酰化,从而调节染色质结构。 | |||
T24636 |
Phostriecin
Sultriecin |
||
Fostriecin is an antifungal and antitumor antibiotic. | |||
TN5680 | Eriobofuran | ||
Eriobofuran, a phytoalexin, has antimicrobialactivity, it can inhibit strongly the spore germination and germ tube growth of Pestalotia funerea, a host-pathogenic fungus of loquat tree. | |||
TN4575 |
Momordicine V
|
Others | Others |
Momordicine V can deter significantly the oviposition by L. trifolii on host plant leaves treated at 26.16 microg/cm2 leaf surface. | |||
TN4437 |
Licorisoflavan A
|
MMP; IL Receptor; NF-κB; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; NF-κB; Proteases/Proteasome |
Licorisoflavan A shows weak scavenging activity against superoxide anion radical, it and licoricidin have potential for the development of novel host-modulating strategies for the treatment of cytokine and/or MMP-mediated disorders such as periodontitis.L | |||
T72581 |
SARS-CoV MPro-IN-2
|
||
SARS-CoVMPro-IN-2 是一种有效的SARS-CoV-2 Mpro 抑制剂,IC50sub>值为 72.07 nM。病毒的主要蛋白酶 Mpro 作为加工病毒多蛋白的主要酶,有助于 SARS-CoV-2 在宿主细胞中的复制和转录,并已被定性为药物发现的有吸引力的靶点。SARS-CoVMPro-IN-2 具有研究 COVID-19 的潜力。 | |||
TN1694 |
Gliotoxin
|
Apoptosis; NF-κB; Wnt/beta-catenin; COX; PKA; Antibacterial; Antifection | Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; Microbiology/Virology; Neuroscience; NF-κB; Stem Cells; Tyrosine Kinase/Adaptors |
Gliotoxin 是一种次生代谢产物,由A. fumigatus 分泌,可以抑制巨噬细胞的吞噬作用和其他免疫细胞的免疫功能。它通过阻止 IκB 降解来抑制诱导型NF-κB 活性,从而诱导宿主细胞凋亡。它可以激活PKA 并增加细胞内 cAMP 浓度,调节肌动蛋白细胞骨架重排以促进A. fumigatus 内化到肺上皮细胞。 | |||
T83693 |
Magainin 2 TFA
MG2 |
||
Magainin 2是一种从非洲爪蟾(X. laevis)皮肤中分离出的阳离子肽,具有宿主防御和抗菌活性。该化合物对细菌E. coli、K. pneumoniae、S. epidermidis、S. aureus及真菌C. albicans表现出活性(MICs分别为5、10、10、50和80 µg/ml)。Magainin 2(20 µM)能降低猕猴桃花粉的萌发率和平均管长。在被单纯疱疹病毒1型(HSV-1)或2型(HSV-2)感染的Vero细胞中,它可减少病毒复制(EC50s分别为22.16和19.8 µM),同时不影响细胞活性,其50%细胞毒性浓度值(CC50)大于100 µM。 |