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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T31011 |
Coralyne chloride
|
Topoisomerase | DNA Damage/DNA Repair |
Coralyne chloride 是一种具有强抗癌活性的原小檗碱。它可用于制备 Coralyne 衍生物,是一种基于荧光 DNA 的分子整流剂,通过位点特异性插入构建成 DNA 双链体。它可作为一种拓扑异构酶 I 毒性分子,诱导拓扑异构酶 I 介导 DNA 裂解。 | |||
T7673 |
ATH686
ATH 686 |
Apoptosis; FLT | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
ATH686 是一种选择性的,ATP 竞争性的FLT3抑制剂,具有抗白血病作用。它靶向突变 FLT3 蛋白激酶活性,并通过诱导凋亡和抑制细胞周期来抑制具有 FLT3 突变的细胞的增殖。 | |||
T8308 |
NL-1
|
Mitochondrial Metabolism; Autophagy | Autophagy; Metabolism |
NL-1 是一种mitoNEET 抑制剂,具有抗白血病作用。它抑制 REH 和 REH/Ara-C 细胞生长,IC50分别为 47.35 µM 和 56.26 µM。 | |||
T24269 |
KPT-251
KPT251 |
Others | Others |
KPT-251 是一种选择性核输出抑制剂。 | |||
T16940 |
STAT5-IN-2
|
Apoptosis; STAT | Apoptosis; JAK/STAT signaling; Stem Cells |
STAT5-IN-2 是一种具有抗白血病作用的 STAT5 抑制剂(EC50:在 K562 和 KU812 细胞中分别为 9 μM 和 5 μM)。 | |||
T15235 |
Enocitabine
|
Nucleoside Antimetabolite/Analog; HCV Protease; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
Enocitabine 是一种核苷类似物,抑制 DNA 复制剂。Enocitabine 抑制人巨细胞病毒的复制,显示出抗白血病和抗病毒活性。 | |||
T27704 |
K00135
K-00135,Imidazol[1,2-b]pyridazine 1,K 00135,IMIDAZOPYRIDAZIN 1 |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
K00135 (IMIDAZOPYRIDAZIN 1) 是 Pim 激酶的选择性抑制剂,可用于胃癌和抗白血病治疗的研究。 | |||
T4409 |
Gilteritinib
吉列替尼,ASP2215 |
FLT; TAM Receptor; c-Kit | Angiogenesis; Tyrosine Kinase/Adaptors |
Gilteritinib (ASP2215) 是一种 FLT3 抑制剂 (IC50:0.29 nM),也是一种 AXL 抑制剂 (IC50:0.73 nM),具有 ATP 竞争性。 | |||
T24492 |
Moflomycin
F 860191,F-860191,F860191 |
||
Moflomycin is an anthracycline derivative. It exhibits a higher antileukemic activity compared to other anthracyclines. | |||
T25503 |
Hisphen
Synonyms Hisfen,MD 2 |
||
Hisphen shows antileukemic activity. | |||
T24978 |
5,10-Dideazaaminopterin
|
||
5,10-Dideazaaminopterin is an antileukemic drug. | |||
T76162 |
Stem bromelain
|
||
茎型菠萝蛋白酶(EC 3.4.22.32),主要自(Ananas comosus)茎中提取的半胱氨酸类蛋白酶,展现广泛纤溶、抗水肿、抗血栓及抗炎活性。此外,具备抗肿瘤、抗白血病及抗转移效能。 | |||
T24979 | 5,10-Dideazafolic acid | ||
5,10-Dideazafolic acid is an antileukemic drug. | |||
T22132 |
PD 166326
|
||
PD166326 是一种吡啶并嘧啶型受体酪氨酸激酶抑制剂,对于Src 和Abl 的IC50值分别为 6 nM 和 8 nM。PD166326 显示出抗白血病活性。 | |||
T40432 |
Mezerein
|
||
Mezerein is a chemical compound with antileukemic properties and acts as a PKC activator. It effectively inhibits the growth of yeast expressing PKC alpha (IC 50 = 1190 nM), PKC beta1 (IC 50 = 908 nM), and PKC delta (IC 50 = 141 nM). However, it does not inhibit the growth of yeast expressing PKC. | |||
T69829 | GCN2iB acetate | ||
GCN2iB is a GCN2 inhibitor. GCN2iB may be useful for the treatment of cancer. The inhibition of GCN2 sensitizes cancer cells with low basal-level expression of asparagine synthetase (ASNS) to the antileukemic agent L-asparaginase (ASNase) in vitro and in vivo. | |||
T15472 |
Hepsulfam
NCI 329680,ZINC01574758 |
Others | Others |
Hepsulfam is an anticancer agent. It also displays excellent antileukemic activity (a median IC50: 0.91 μg/mL in a panel of different tumors). | |||
T60559 |
S-(N-PhenethylthiocarbaMoyl)-L-cysteine
|
||
S-(N-PhenethylthiocarbaMoyl)-L-cysteine (PEITC-Cys) 是一种抗癌剂。S-(N-PhenethylthiocarbaMoyl)-L-cysteine 具有抗白血病活性,可抑制 HL60 细胞中的 DNA 合成。S-(N-PhenethylthiocarbaMoyl)-L-cysteine 是P450的抑制剂。 | |||
T78733 |
ZLD115
|
||
ZLD115(化合物44)为FB23衍生的FTO抑制剂,作为抗白血病药物,对白血病细胞系展示抗增殖效果。 | |||
T25170 |
Botryodiplodin
Cytostipin,Antibiotic PSX 1 |
||
Botryodiplodin, an antibiotic, has antileukemic activity from Botryodiplodia theobromae. It has the property of turning the skin of the individual in various shades of pink 2-3 hrs after application. It is a toxic metabolite of Penicillium carneo-lutescen | |||
T73167 |
HDAC-IN-49
|
||
HDAC-IN-49 是一种有效的非选择性 HDAC(HDAC) 抑制剂,对 HDAC1、HDAC2、HDAC3、HDAC4 和 HDAC6的 IC50分别为 13 nM、14 nM、21 nM、1880 nM 和 10 nM 。HDAC-IN-49 表现出显着的抗白血病活性, 但对健康细胞具有低细胞毒性。 | |||
T73358 |
(-)SHIN2
|
||
(-)SHIN2 是 (+)SHIN2 的异构体。(+)SHIN2 是丝氨酸羟甲基转移酶 (SHMT) 的抑制剂,具有抗白血病作用。(+)SHIN2 与 Methotrexate 在体内异种移植模型中具有协同作用。 | |||
T82774 | Caspase-3 activator 3 | Caspase | Apoptosis; Proteases/Proteasome |
Caspase-3 activator 3 (compound 2h) 通过激活caspase 3诱导HL-60和K562细胞apoptosis,表现出抗白血病活性。其对HL-60细胞的IC50值为42.89 μM,对K562细胞的IC50值为33.61 μM。 | |||
T4791 |
Idarubicin
Demethoxydaunorubicin |
||
Idarubicin 是一种有效的、具有口服活性的蒽环类抗白血病剂。Idarubicin 抑制拓扑异构酶 II,干扰 DNA 复制和 RNA 转录。Idarubicin 可诱导 DNA 损伤。Idarubicin 抑制 DNA 合成和 c-myc 表达。Idarubicin 还抑制细菌和酵母菌的生长。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1932 |
Microhelenin C
|
Others | Others |
Microhelenin C 是抑制从Helenium microcephalum 中提取的倍半萜内酯,具有抗肿瘤作用。 | |||
TN4673 |
(+)-Nortrachelogenin
Wikstromol,荛花酚 |
Apoptosis; HIV Protease; PI3K; Antifection | Apoptosis; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
(+)-Nortrachelogenin 是一种从 Wikstroemia indica C.A. Meyer (百里香科)中分离出来的木脂素。 (+)-Nortrachelogenin 具有抗白血病活性。 | |||
T5S1058 |
Triptonide
雷公藤内酯酮,PG 492,NSC 165677 |
Apoptosis; Wnt/beta-catenin; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; Stem Cells |
Triptonide (PG 492) 是从雷公藤中鉴定出的一种天然产物,是一种 Wnt 信号抑制剂,其 IC50约为 0.3 nM。它具有免疫抑制、抗炎、避育、神经保护和抗淋巴瘤作用。 | |||
TN2319 |
Yadanzioside A
鸦胆子苷A,鸦胆子内脂A |
Others | Others |
Yadanzioside A has antileukemic activity. | |||
TN5266 |
Yadanzioside F
|
Others | Others |
Yadanzioside F has antileukemic activity. | |||
TN3780 | Deacetyleupaserrin | Others | Others |
Deacetyleupaserrin is an antileukemic sesquiterpene lactone. | |||
TN5265 | Yadanzioside C | Others | Others |
Yadanzioside C has antileukemic activity. | |||
TN2320 |
Yadanzioside G
|
Others | Others |
Yadanzioside G has antileukemic activity. | |||
TN4027 |
Eucannabinolide
|
Others | Others |
Eucannabinolide exhibits in vivo antileukemic activity. | |||
TN3796 | Dehydrobruceantinol | Others | Others |
Dehydrobruceantinol shows bitter taste and has antileukemic activity. | |||
TN3542 |
Bruceantinoside A
|
Others | Others |
Bruceantinoside A has antileukemic activity. | |||
TN5092 | Tagitinin F | Antifection | Microbiology/Virology |
Tagitinin F possesses antileukemic activity; it also shows in vitro leishmanicidal activities against Leishmania braziliensis promastigotes and amastigotes. | |||
TN5270 |
Yadanzioside P
|
Others | Others |
Yadanzioside P has antileukemic and antitumor activities. | |||
TL0014 | Pinusolide | ERK; p38 MAPK; Calcium Channel; Lipoxygenase; PAFR; Caspase; JNK; AMPK | Apoptosis; Chromatin/Epigenetic; GPCR/G Protein; MAPK; Membrane transporter/Ion channel; Metabolism; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Pinusolide is a platelet activating factor ( PAF) antagonist, it may prove of therapeutic value in the treatment of hypotension, it has antileukemic potential, and could be used to treat neurodegenerative diseases. Pinusolide attenuates blockade of insulin signaling by enhancing IRS-1 tyrosine phosphorylation by the activating the AMPK pathway, indicates the targeting of AMPK represents a new therapeutic strategy for hyperglycemia-induced insulin resistance and type 2 diabetes. |