97
17
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2747 |
Endothall
|
Others | Others |
Endothall 是一种有效的蛋白磷酸酶 2A (PP2A) 抑制剂,对 PP2A 和 PP1 具有抑制作用, IC50 分别为 90 nM 和 5 µM。Endothall 具有抗癌活性,可用于癌症化疗,可用作除草剂。 | |||
T21876 |
DC_AC50
|
Apoptosis; Others | Apoptosis; Others |
DC_AC50 是一种 Atox 和 CCS 的双抑制剂,是一种抑制细胞内铜伴侣作为减少/预防获得性化疗耐药性的手段。它与 Atox1 和 CCS 结合并减少癌细胞增殖和肿瘤生长。 | |||
T22746 |
Tesmilifene fumarate
DPPE fumarate |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Tesmilifene fumarate (DPPE fumarate) 是一种 H1C 受体拮抗剂,可增强化疗的细胞毒性且保护正常细胞。 | |||
T9271 |
RAD51-IN-1
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
RAD51-IN-1 是 B02 的衍生物,是一种RAD51的有效抑制剂,可研究癌症。 | |||
T1564 |
Cisplatin
cis-Diaminodichloroplatinum,CDDP,顺铂 |
DNA Alkylator/Crosslinker; Ferroptosis; DNA/RNA Synthesis; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Cisplatin (CDDP) 是一种 DNA 交联剂。Cisplatin 具有抗肿瘤活性,能够通过在癌细胞中形成 DNA 加合物来抑制 DNA 合成。Cisplatin 还可激活铁死亡并诱导自噬。 | |||
T1414 |
Sodium 2-mercaptoethanesulfonate
Mitexan,美司那,美司钠,Uromitexan,Mesna,Mesnum,Mesnex |
Others | Others |
Sodium 2-mercaptoethanesulfonate (Uromitexan) 是一种抗氧化剂,具有细胞保护作用。它可用于减轻由环磷酰胺引起的出血性膀胱炎。它广泛用作抗化学疗法毒性的全身保护剂。 | |||
T1528 |
Azasetron hydrochloride
Y-25130 hydrochloride,Y-25130 HCl,盐酸阿扎司琼,Azasetron HCl |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Azasetron hydrochloride (Y-25130 HCl) 是一种苯甲酰胺的衍生物,是有效的、选择性的5-HT3受体拮抗剂,可用于化疗引起的恶心呕吐研究。 | |||
T2047 |
AG-1478
AG1478,NSC 693255,Tyrphostin AG-1478 |
EGFR; HCV Protease; Influenza Virus; HER; PDGFR | Angiogenesis; JAK/STAT signaling; Microbiology/Virology; Proteases/Proteasome; Tyrosine Kinase/Adaptors |
AG-1478 (NSC-693255) 是一种选择性 EGFR 酪氨酸激酶抑制剂,IC50为 3 nM。它对 HCV 和脑心肌炎病毒有抗病毒作用。 | |||
T1478 |
Ondansetron hydrochloride dihydrate
盐酸昂丹司琼,SN 307,NSC 665799,GR 38032,Ondansetron hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ondansetron hydrochloride dihydrate (GR 38032) 是5- HT3受体拮抗剂,可治疗化疗后的恶心和呕吐,有抗焦虑和抗精神病作用。 | |||
T1790 |
Fosaprepitant dimeglumine
福沙匹坦二甲葡胺,L785298,福沙吡坦二甲葡胺,MK-0517,Fosaprepitant dimeglumine salt |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Fosaprepitant dimeglumine (MK-0517) 是 Aprepitant 的前药。它是一种神经激肽 1 受体拮抗剂,可用于预防化疗引起的恶心呕吐。 | |||
T16871 |
Semustine
|
DNA Alkylator/Crosslinker | DNA Damage/DNA Repair |
Semustine 是一种 DNA 烷化剂,是一种癌症化疗化合物,在接受辅助化疗的恶性黑色素瘤患者中具有肾毒性,可用于辅助治疗白血病。 | |||
T21899 |
Misonidazole
SR-1354,SR1354,Ro 7-0582 |
GPX | oxidation-reduction |
Misonidazole 是一种缺氧肿瘤细胞放射增敏剂,具有抗菌活性。 | |||
T22313 |
Dolasetron Mesylate
多拉司琼甲磺酸盐,甲磺酸多拉司琼,Anzemet hydrate,MDL-73147EF |
Others; 5-HT Receptor | GPCR/G Protein; Neuroscience; Others |
Dolasetron Mesylate (MDL-73147EF) 是 5-HT3 受体的拮抗剂,可用于治疗化疗后呕吐和恶心的研究。 | |||
T28187 |
Nonabine
|
||
Nonabine 是一种具有强烈止吐作用的化合物,可用来预防与癌症化疗有关的恶心和呕吐。 | |||
T68068L |
(R)-CJ 11974
|
Neurokinin receptor | GPCR/G Protein; Neuroscience |
T24184 |
Itasetron
DAU6215CL,UNII-00S0D0OEKR,U-98079A,U 98079A,DAU 6215CL |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Itasetron (U 98079A) 是一种5-羟色胺3受体拮抗剂,可用于预防大鼠与年龄有关的记忆缺陷。Itasetron 在癌症化疗和放疗动物模型中的止吐活性,可用于研究健忘症。 | |||
T4568 |
Dolasetron
MDL-73147,多拉司琼 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Dolasetron (MDL-73147) 是一种血清素 5-HT3 受体拮抗剂,用于治疗化疗后的恶心和呕吐。 | |||
T10244 |
ACY-1083
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
ACY-1083 是一种选择性和脑穿透性 HDAC6 抑制剂 (IC50:3 nM),可有效逆转化疗引起的周围神经病变。 | |||
T39024 |
PrNMI
|
Cannabinoid Receptor | GPCR/G Protein |
PrNMI is a highly effective and orally active agonist targeting the peripherally restricted cannabinoid 1 receptor (CB1R). It exhibits pronounced analgesic properties, efficiently suppressing both chemotherapy-induced peripheral neuropathy pain symptoms and cancer-induced bone pain. | |||
T6616 |
Ondansetron hydrochloride
SN 307,盐酸昂丹司琼,帕罗西汀杂质A,Ondansetron HCl,Emeset,GR 38032 HCl,NSC 665799,Zofran |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ondansetron hydrochloride (Zofran) 是5-HT3受体的拮抗剂,可用作化疗后止吐剂。 | |||
T1755 |
LY2090314
|
GSK-3 | PI3K/Akt/mTOR signaling; Stem Cells |
LY2090314 是GSK-3抑制剂,抑制 GSK-3α (IC50:1.5 nM) 和 GSK-3β (IC50:0.9 nM)。 | |||
T1042 |
Granisetron hydrochloride
盐酸格拉司琼,BRL 43694A,Granisetron HCl |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Granisetron hydrochloride (Granisetron HCl) 是一种5-HT3受体拮抗剂,可作为化疗后止吐剂。 | |||
T28935 | TDRL-551 | Others | Others |
TDRL-551 是一种新型有效的复制蛋白A (RPA) 抑制剂 (IC50=18 µM),具有潜在的抗癌活性。TDRL-551 对 RPA-DNA 相互作用有抑制作用,提高以铂为基础的肺癌和卵巢癌化疗的疗效。 | |||
T0776 |
Phenothiazine
ENT 38,吩噻嗪 |
Dopamine Receptor; Antibacterial; Antibiotic; Antifungal | GPCR/G Protein; Microbiology/Virology; Neuroscience |
Phenothiazine (ENT 38) 是一种抗生素,具有杀虫,抗菌,驱虫和杀真菌活性。它也可研究神经系统疾病。 | |||
T3716 |
Rolapitant
罗拉吡坦,SCH619734,罗拉匹坦 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Rolapitant (SCH619734) 是一种高效选择性具有口服活性的神经激肽 1 受体抑制剂,Ki 值为0.66 nM。 | |||
T6127 |
Rucaparib Phosphate
AG-014699 phosphate,PF-01367338,芦卡帕利,AG-014699,瑞卡帕布磷酸盐,PF-01367338 phosphate |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Rucaparib Phosphate (PF-01367338 phosphate) 是一种口服有效的PARP 蛋白抑制剂,对 PARP-1 的Ki 为 1.4 nM。它是六磷酸己糖脱氢酶 (H6PD) 抑制剂,有用于去势抵抗性前列腺癌 (CRPC) 的研究潜力。 | |||
T76788 |
Demcizumab
OMP 21M18 |
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
Demcizumab (OMP 21M18) 是一种抗 DLL4 单克隆抗体。Demcizumab 是一种有效的 Notch 通路抑制剂。Demcizumab 在多种癌症模型中无论使单独还联合化疗试剂使用都是有效的。 | |||
T2589 |
Dolasetron Mesylate hydrate
Dalasetron Mesylate Hydrate,多拉司琼甲磺酸盐一水合物 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Dolasetron Mesylate hydrate (Dalasetron Mesylate Hydrate) 是一种选择性血清素受体拮抗剂,可竞争性阻断血清素对 5HT3 受体的作用,从而抑制化疗和放疗引起的恶心和呕吐。 | |||
T9955 |
EX-A5758
|
NOS | Immunology/Inflammation |
EX-A5758是一种新型推定的小分子 nNOS-NOS1 AP 抑制剂,可抑制炎症性伤害感受和化疗引起的神经性疼痛,并与紫杉醇协同降低肿瘤细胞活力 | |||
T4451 |
Estramustine phosphate sodium
Ro 21-8837/001,Estramustine phosphate disodium,雌莫司汀磷酸钠 |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Estramustine phosphate sodium (Ro 21-8837/001) 是雌二醇类似物,是一种具有口服活性抗微管化疗剂,通过与微管相关蛋白和微管蛋白结合而使微管解聚。它可诱导前列腺癌细胞凋亡,可研究前列腺癌。 | |||
T4684 |
ML241 hydrochloride
|
p97 | Ubiquitination |
ML241 hydrochloride 是一种有效且选择性的 p97 ATPase 抑制剂,IC50值为 100 nM。 | |||
T15611 |
JH-RE-06
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
JH-RE-06是一种REV1-REV7互作抑制剂,IC50为0.78 μM,Kd 为0.42 μM。它靶向与 POLζ 的 REV7 亚基相互作用的 REV1,可改善化疗效果。它通过阻止诱变 POLζ 的募集来破坏诱变性跨损伤合成。 | |||
T2283 |
PX-12
2-[(1-甲基丙基)二硫代]-1H-咪唑,IV-2,PX12 |
Thioredoxin | Metabolism |
PX-12 (PX12) 是一种可逆的硫氧还蛋白-1(Trx-1)抑制剂,能够抑制 MCF-7 细胞(IC50:1.9 μM)和HT-29 细胞(IC50:2.9 μM)的生长。 | |||
T2265 |
Bimiralisib
5-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine,PQR309,PI3K-IN-2 |
Others; PI3K; S6 Kinase; mTOR | MAPK; Others; PI3K/Akt/mTOR signaling |
Bimiralisib (PI3K-IN-2) 是一种有效的,可渗透脑的 mTOR/PI3K 抑制剂,是一种 mTORC1和 mTORC2抑制剂。它能够抑制 PI3Kα,PI3Kδ,PI3Kβ,PI3Kγ和 mTOR,IC50分别为 33 nM,451 nM,661 nM,708 nM 和 89 nM。 | |||
T3614 |
Inosine pranobex
Groprinosin,Isoprinosine,异丙肌苷,Immunovir,Delimmun |
IL Receptor; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Inosine pranobex (Delimmun) 是一种免疫增强剂,它是一种广谱抗病毒剂,用于 HIV 感染。 | |||
T31977 |
GLYN
NSC 137875,NSC137875,Glycidyl nitrate,NSC-137875 |
||
GLYN, a nitric oxide donor, acts by enhancing the therapeutic efficacy of chemotherapy and radiotherapy. | |||
T26283 |
TNP-351
Tnp 351 |
||
Tnp 351 is a novel antifolate drug being assessed for chemotherapy of lung cancer. | |||
T1120L |
Dacarbazine hydrochloride
Dacarbazine HCl |
||
Dacarbazine ( imidazole carboxamide) is a chemotherapy drug used to treat melanoma and Hodgkin's lymphoma. | |||
T29486 |
7-Methotrexate
7-Mtx |
||
7-Methotrexate is used as a chemotherapy agent and immune system suppressant. It is used to treat cancer, autoimmune diseases, ectopic pregnancy, and medical abortions. | |||
T22393 |
Palonosetron
RS25259,帕洛诺司琼,RS 25259 197 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Palonosetron, a 5-HT3 antagonist with Ki of 0.17 nM, is used in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV). | |||
T29391 |
3'-Chloromethotrexate
NSC 29631,NSC29631,SKI 23338,NSC-29631,AI3-50533 |
||
3'-Chloromethotrexate is a chemotherapy agent and immune system suppressant. It can be used to treat cancer, autoimmune diseases, ectopic pregnancy, and medical abortions. | |||
T22340 |
Granisetron
Sustol,Granisetronum,格拉司琼,Sancuso,Kevatril |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Granisetron, a serotonin receptor (5HT-3 selective) antagonist, is used as an antinauseant and antiemetic for cancer chemotherapy. | |||
T68274 |
QZ59S-SSS
|
||
QZ59S-SSS acts as a potential inhibitor of human P-glycoprotein and may be used to improve the efficacy of cancer chemotherapy. | |||
T70114 |
Paclitaxel Ceribate
|
||
Paclitaxel Ceribate is a mitotic inhibitor used in cancer chemotherapy. | |||
T25929 |
Pemetrexed tromethamine
Pemetrexed ditromethamine dihydrate |
||
Pemetrexed tromethamine is a chemotherapy drug used for pleural mesothelioma and non-small cell lung cancer. | |||
T30041 |
Amphoglucamine
|
||
Amphoglucamine is used in the combined chemotherapy of viral diseases. | |||
T13161 |
Tin-protoporphyrin IX
锡原卟啉IX,SnPPIX |
Others | Others |
Tin-protoporphyrin IX is a potent inhibitor of Heme oxygenase-1 (HO-1). It sensitizes pancreatic ductal adenocarcinoma (PDAC) tumors to chemotherapy in mice models. | |||
T31837 |
FOLFIRI Regimen
FOLFIRI |
||
FOLFIRI Regimen is a chemotherapy regimen consisting of leucovorin calcium (calcium folinate), 5-fluorouracil, and irinotecan used during the treatment of advanced-stage and metastatic colorectal cancer. | |||
T71123 |
RG 12915
|
||
RG 12915 is a potent, selective 5-HT3 receptor antagonist developed for the treatment of emesis and nausea associated with cancer chemotherapy. | |||
T33326 |
Methotrexate-alpha glutamate
Meapa-glu-glu |
||
Methotrexate-alpha glutamate is a chemotherapy agent and immune system suppressant. It is used to treat cancer, autoimmune diseases, ectopic pregnancy, and medical abortions. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2217 |
Cephalomannine
Baccatin III,三尖杉宁碱 |
Microtubule Associated | Cytoskeletal Signaling |
Cephalomannine (Baccatin III) 是一种从云南红豆杉中提取的紫杉醇衍生物,具有抗肿瘤活性,可用于癌症研究。 | |||
T21936 |
M50054
2,2′-亚甲基双(1,3-环己二酮) |
Caspase | Apoptosis; Proteases/Proteasome |
M50054 是一种有效的细胞凋亡抑制剂,可用于研究抗 Fas 抗体引起的肝炎和化疗引起的脱发。它抑制 Etoposide 诱导的 U937 细胞 caspase-3 活化,IC50为 79 μg/mL。 | |||
T0132 |
Etoposide
VP-16,依托泊苷,依托泊甙,VP-16-213 |
Apoptosis; Mitophagy; Topoisomerase; Antibacterial; Antibiotic; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Microbiology/Virology |
Etoposide (VP-16-213) 是一种拓扑异构酶 II 的抑制剂,通过与拓扑异构酶 II 和 DNA 形成复合物来抑制 DNA 合成 (IC50=60.3 μM)。Etoposide 具有抗肿瘤活性,可以诱导细胞凋亡、自噬。 | |||
T6431 |
Levoleucovorin Calcium
左亚叶酸钙,Calcium Levofolinate,CL307782 |
Others; Antifolate | Cell Cycle/Checkpoint; Others |
Levoleucovorin Calcium (CL307782) 是一种亚叶酸的钙盐,在癌症化疗中用作辅助剂。 | |||
T22286 |
Cyanosafracin B
Cyanoquinonamine,氰基番红菌素 B,CBR28-1 |
Others | Others |
Cyanosafracin B (Cyanoquinonamine) 是一种合成 Phthalascidin Pt-650 及 Ecteinascidin ET-743 的起始原料。 | |||
T1285 |
Anethole trithione
茴三硫,Anetholtrithion |
Others; AChR | Neuroscience; Others |
Anethole trithione (Anetholtrithion) 是硫杂环胆碱,是一种胆汁分泌刺激剂,可增强唾液分泌并增加 mAChR 受体,用于口干症的研究。 | |||
T1156 |
Palonosetron hydrochloride
盐酸帕洛诺司琼,RS 25259 197,Palonosetron HCl,RS 25259 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Palonosetron hydrochloride (RS 25259) 是一种 5-HT3 拮抗剂,用于预防和治疗化疗引起的恶心和呕吐。 | |||
T3924 |
Astragaloside II
黄芪皂苷 II,Astrasieversianin VIII |
TGF-beta/Smad | Stem Cells |
Astragaloside II (Astrasieversianin VIII) 是一种分离自黄芪中的天然化合物。 | |||
T4S0094 |
Hydroxygenkwanin
羟基芫花素,Luteolin 7-methylether,7-O-Methylluteolin |
Antioxidant | oxidation-reduction |
Hydroxygenkwanin (Luteolin 7-methylether) 是一种丁香达芙妮的主要成分,是一种天然的类黄酮化合物。它具有抗氧化,抗神经胶质瘤能力和抗癌作用。 | |||
T2S1120 |
Ganoderenic acid B
|
P-gp | Membrane transporter/Ion channel; Neuroscience |
Ganoderenic acid B 是一种从Ganoderma lucidum 中提取的天然产物,可以通过抑制ABCB1的转运功能,增强化疗药物对ABCB1介导的耐多药癌细胞的细胞毒性来发挥作用。 | |||
T3729 |
Ethyl gallate
Nipagallin A,Phyllemblin,gallic acid ethyl ester,没食子酸乙酯 |
MMP; NF-κB; Akt; Antibacterial | Cytoskeletal Signaling; Microbiology/Virology; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Ethyl gallate (gallic acid ethyl ester) 是一种非类黄酮酚过氧化氢清除剂。 | |||
T2563 |
Acetyl-L-carnitine hydrochloride
Acetyl L-carnitine hydrochloride,O-Acetylcarnitine,乙酰-L-肉(毒)碱盐酸盐,O-acetyl-L-carnitine,O-Acetyl-L-carnitine hydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Acetyl-L-carnitine hydrochloride (Acetyl L-carnitine hydrochloride) 是一种由内源性左旋肉碱的乙酰化形式的盐酸盐组成的营养补充剂,具有潜在的神经保护、认知增强、抗抑郁和免疫调节活性。还可缓解化疗、糖尿病或其他疾病引起的周围神经病变。此外,乙酰左旋肉碱可能通过增加T淋巴细胞成熟来调节免疫反应,并可能下调促炎细胞因子对病毒(如SARS-CoV-2)的反应。它还可能破坏ACE2信号通路并抑制活性氧(ROS)的产生。 | |||
T37984 |
D-Fructose-1,6-bisphosphate sodium salt hydrate
|
Others | Others |
D-Fructose-1,6-bisphosphate sodium salt hydrate 是碳水化合物代谢的中间体,包括糖酵解和糖异生。在糖酵解过程中,它是由磷酸果糖激酶磷酸化果糖-6-磷酸产生的。由果糖-1,6-二磷酸酶-1介导的逆反应是糖异生的限速步骤之一。同样的反应也发生在植物的叶绿体中,D-Fructose-1,6-bisphosphate sodium salt hydrate 作为还原性戊糖磷酸循环的一部分。由于癌细胞采用糖酵解作为代谢能量产生的主要来源,这一途径已成为癌症化疗的主要靶点。 | |||
T35000 |
Uproleselan sodium
GMI 1271,GMI1271,GMI-1271 |
||
Uproleselan sodium (GGI-1271) is a small molecule E-selector antagonist originally targeted at AML as an adjuvant to standard chemotherapy for hematological malignancies. | |||
T3S0205 |
β-Hederin
Beta-Hederin,β-常春藤素 |
Parasite | Microbiology/Virology |
β-Hederin 是从 Hedera helix L.(Araliaceae) 分离得到的一种皂苷,具有抗利什曼虫活性。它对乳腺癌细胞有凋亡作用,有望成为乳腺癌化疗的候选药物。 | |||
T4735 |
2'-Deoxyuridine 5'-monophosphate disodium
2'-脱氧尿苷-5'-单磷酸二钠,2'-dUMP⋅2Na,2-脱氧尿嘧啶核苷-5'-单磷酸二钠盐,2'-Deoxyuridine 5'-monophosphate disodium salt |
Others; Endogenous Metabolite | Metabolism; Others |
2'-Deoxyuridine 5'-monophosphate disodium (2'-dUMP⋅2Na) salt 能够被双底物酶胸苷酸合酶(TS) 还原甲基化为 dTMP (2'-deoxythymidine 5'-monophosphate)。其中 dTMP 是 DNA 合成所需的核苷酸。 | |||
T66078 | Cardamonin | ||
Cardamonin, a chalcone extracted from cardamom spice with anti-inflammatory and anti-tumor activities. Cardamonin decreased viability of NPC(Nasopharyngeal carcinoma ) cells in a concentration-dependent manner. The IC50 values were 16.22 μM(CNE-1), 14.34 μM (CNE-2), 16.50 μM (HONE-1), and 68.12 μM (SUNE-1). Moreover, the expression level of the proapoptotic effector protein Bax and Bid was also markedly increased after treatment with cardamonin(15μM) in CNE-2 cells.In vivo, cardamonin (25 mg/kg ... |