Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T29168 |
XR-5000
NSC-601316,CRC8805,SN-22995,DACA,CRC-8805 |
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XR-5000 is a DNA topoisomerase I and II inhibitor. | |||
T2320 |
Indacaterol
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Indacaterol 是一种超长效β-肾上腺素受体激动剂。 | |||
T36898 |
Sandacanol
Sandranol,2-Ethyl-4-(2,2,3-trimethylcyclopent-3-en-yl)-but-2-en-1-ol |
Apoptosis | Apoptosis |
Sandacanol(Sandranol) 是一种选择性嗅觉受体(OR10H1)激动剂。Sandacanol可诱导膀胱癌细胞的细胞周期停止和部分凋亡,可降低细胞迁移率和增殖率。 | |||
T1239 |
Indacaterol maleate
马来酸茚达特罗,QAB149 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Indacaterol maleate (QAB149) 是一种超长效的 β-肾上腺素受体激动剂。 | |||
T1120 |
Dacarbazine
Imidazole Carboxamide,达卡巴嗪,DTIC-Dome |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Dacarbazine (DTIC-Dome) 是一种抗肿瘤剂,对黑色素瘤具有显着的活性。 | |||
T1120L |
Dacarbazine hydrochloride
Dacarbazine HCl |
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Dacarbazine ( imidazole carboxamide) is a chemotherapy drug used to treat melanoma and Hodgkin's lymphoma. | |||
T71658 |
Indacaterol xinafoate
|
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Indacaterol xinafoate is an ultra-long-acting beta-adrenoceptor agonist. | |||
T71660 |
Indacaterol fumarate
|
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Indacaterol fumarate is an ultra-long-acting beta-adrenoceptor agonist. | |||
T71659 |
Indacaterol acetate
|
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Indacaterol acetate is an ultra-long-acting beta-adrenoceptor agonist. | |||
T1120L2 |
Dacarbazine citrate
DTIC citrate |
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Dacarbazine citrate is an alkylating agent used to treat cancers of the lymphatic system and malignant melanoma (a type of skin cancer) in patients with certain conditions: islet cell carcinoma (part of the pancreas) Soft tissue sarcoma (cancer of muscles | |||
T36695 |
TAS-103
|
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TAS-103 is a dual inhibitor of DNA topoisomerase I/II, used for cancer research. TAS-103 is a dual inhibitor of DNA topoisomerase I/II. TAS-103 (0.1-10 μM) is active on CCRF-CEM cells, with an IC50 value of 5 nM. TAS-103 (0.1 μM) significantly increases levels of topo IIα FITC immunofluorescence in individual CCRF-CEM cells[1]. TAS-103 (0.01-1 μM) is highly cytotoxic to Lewis lung carcinoma (LLC) cells, and Liposomal TAS-103 is almost as active as free TAS-103[2]. TAS-103 inhibits the viability ... |