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T17253WAY 163909；化合物 T17253WAY 163909
WAY 163909 is an effective and selective agonist of the 5-HT(2C) receptor (Ki: 10.5±1.1 nM).
价 格：￥电议型 号：T17253产 地：中国大陆
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T17190U18666A；化合物U18666AU18666A
U18666A is a cell-permeable drug and is a cholesterol synthesis and transport inhibitor. It inhibits replication of Ebola virus, dengue virus, and human hepatitis C virus.
价 格：￥电议型 号：T17190产 地：中国大陆
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T17159Treosulfan；曲奥舒凡NSC 39069|||Treosulphan；NSC 39069|||曲奥舒凡|||Treosulphan
Treosulfan (Treosulphan) is a bifunctional alkylating agent. It also has activity in ovarian cancer and other solid tumor types.
价 格：￥电议型 号：T17159产 地：中国大陆
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T17059Tetrahydrouridine；四氢尿苷NSC 112907|||NSC112907|||NSC-112907；NSC 112907|||NSC112907|||四氢尿苷|||NSC-112907
Tetrahydrouridine (NSC-112907; THU) is a multidrug resistance modulator. It can be used in cancer treatment to make tumor cells more sensitive to radiation therapy. THU is a competitive cytidine deaminase(CDA) inhibitor that inhibits deamination in the catabolism of cytotoxic deoxycytidine analogs such as ara-C and Gemcitabine.
价 格：￥电议型 号：T17059产 地：中国大陆
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T17029Tegobuvir；化合物TegobuvirGS-9190|||GS 333126；GS-9190|||GS 333126|||5-[[6-[2,4-双(三氟甲基)苯基]-3-哒嗪基]甲基]-2-(2
Tegobuvir (GS 333126) is a specific and covalent HCV NS5B polymerase inhibitor.
价 格：￥电议型 号：T17029产 地：中国大陆
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T16998Tauroursodeoxycholate dihydrate；牛磺熊去氧胆酸二水合物Taurolite dihydrate|||TUDCA dihydrate|||UR 906 dihydrate；
Tauroursodeoxycholate dihydrate is an endoplasmic reticulum stress inhibitor. Tauroursodeoxycholate also inhibits ERK. Tauroursodeoxycholate significantly decreases the expression of apoptosis molecules, such as caspase-3 and caspase-12.
价 格：￥电议型 号：T16998产 地：中国大陆
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T16990Tarafenacin；化合物 T16990SVT-40776；SVT-40776
Tarafenacin is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over the M2 receptor.
价 格：￥电议型 号：T16990产 地：中国大陆
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T16978Talaporfin sodium；他拉泊芬钠ME2906|||NPe6|||Mono-L-aspartyl chlorin e6；ME2906|||他拉泊芬钠|||NPe6|||Mono-L-asp
Talaporfin is a photosensitizer used in photodynamic therapy.
价 格：￥电议型 号：T16978产 地：中国大陆
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T16961Supinoxin；化合物SupinoxinRX-5902；RX-5902
Supinoxin (RX-5902) is an orally active inhibitor of phosphorylated-p68 RNA helicase and a potent first-in-class anti-cancer agent. Supinoxin induces cell apoptosis and inhibits the growth of TNBC cancer cell lines (IC50s:10 nM - 20 nM).
价 格：￥电议型 号：T16961产 地：中国大陆
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T1693Umbelliferone；7-羟基香豆素Skimmetine|||Hydrangin|||Hydrangine|||7-Hydroxycoumarin|||NSC 19790；Skimmetine|
Umbelliferone (7-Hydroxycoumarin) is found in anise. Umbelliferone occurs widely in plants including Angelica species Phytoalexin of infected sweet potat. It has been reported to have antioxidant properties.
价 格：￥电议型 号：T1693产 地：中国大陆
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T16909Donafenib；多纳非尼Sorafenib (D3)|||Bay 43-9006 (D3)|||Sorafenib-d3；Sorafenib (D3)|||Bay 43-9006 (D3)|||S
Donafenib (Bay 43-9006 (D3)) is a deuterium-labeled Sorafenib which is a multikinase inhibitor(IC50s: 6 nM, 20 nM, and 22 nM for Raf-1, B-Raf, and VEGFR-3, respectively).
价 格：￥电议型 号：T16909产 地：中国大陆
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T16907Soluflazine；化合物 T16907Soluflazine
Soluflazine is a nucleoside transport inhibitor. It also has anticonvulsant action.
价 格：￥电议型 号：T16907产 地：中国大陆
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T16906Sograzepide；化合物 T16906YM-220|||Netazepide|||YF 476；YM-220|||Netazepide|||YF 476
Sograzepide is an effective and highly selective Gastrin/CCK-B antagonist (IC50: 0.1 nM), has an inhibitory effect on Gastrin/CCK-A activity (IC50: 502 nM). Sograzepide replaces the specific binding of [125I]CCK-8 to the rat brain, cloned canine, and cloned human Gastrin/CCK-B receptors (Ki: 0.068, 0.62 and 0.19 nM, respectively).
价 格：￥电议型 号：T16906产 地：中国大陆
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T16905SNIPER(BRD)-1；化合物 T16905SNIPER(BRD)-1
SNIPER(BRD)-1 is a chemical compound composed of a derivative of the IAP antagonist LCL-161 and the BET inhibitor (+)-JQ-1, linked together. It promotes the degradation of BRD4 through the ubiquitin-proteasome pathway and effectively degrades cIAP1, cIAP2, and XIAP with IC50 values of 6.8 nM, 17 nM, and 49nM, respectively[1].
价 格：￥电议型 号：T16905产 地：中国大陆
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T16904Smurf1-IN-A01；化合物Smurf1-IN-A01A01；A01
Smurf1-IN-A01 (A01) is a ubiquitin ligase Smad ubiquitination regulatory factor-1 inhibitor (kd: 3.664 nM). It increases BMP-2 responsiveness by inhibiting Smurf1-mediated Smad1/5 degradation.
价 格：￥电议型 号：T16904产 地：中国大陆
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T16903SMPH Crosslinker；化合物 T16903SMPH Crosslinker
SMPH Crosslinker is an alkyl/ether-based PROTAC linker utilized for synthesizing PROTACs[1].
价 格：￥电议型 号：T16903产 地：中国大陆
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T16901SMIP004；化合物SMIP004SMIP004
SMIP004 is an SKP2 E3 ligase inhibitor. SMIP004 is a cancer cell-selective apoptosis inducer of human prostate cancer cells.
价 格：￥电议型 号：T16901产 地：中国大陆
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T16900SMER18；化合物 T16900SMER18
SMER18 is a small molecule enhancer of rapamycin which acts as an mTOR-independent autophagy inducer.
价 格：￥电议型 号：T16900产 地：中国大陆
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T1690BroMhexine IMpurity B；盐酸氨溴索杂质标准品EBroMhexine IMpurity B
Bromhexine Impurity B reagent used in the preparation of Ambroxol and Bromhexine (B678600) metabolites Ambroxol EP Impurity E.
价 格：￥电议型 号：T1690产 地：中国大陆
