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T2112Fexinidazole；非昔硝唑HOE 239；非昔硝唑|||HOE 239
Fexinidazole (HOE 239) is an antiparasitic agent. It has activity against Trypanosoma cruzi, Tritrichomonas foetus, Trichomonas vaginalis, Entamoeba histolytica, Trypanosoma brucei, and Leishmania donovani. The biologically relevant active metabolites in vivo are the sulfoxide and sulfone.
价 格：￥电议型 号：T2112产 地：中国大陆
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T21112Triprolidine hydrochloride；盐酸曲普利啶295 C 51|||Pro-Entra|||Entra|||Actidilat|||Triprolidine hydrochlori
Triprolidine hydrochloride anhydrous, a Histamine H1 antagonist, is used in asthma, allergic rhinitis, and urticaria.
价 格：￥电议型 号：T21112产 地：中国大陆
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T20360Chlorodiphenylmethane；化合物 T20360AI311230|||AI3-11230|||AI3 11230；AI311230|||AI3-11230|||AI3 11230
Chlorodiphenylmethane is an organic compound. It has two phenyl rings.
价 格：￥电议型 号：T20360产 地：中国大陆
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T20112Triphenyl bismuth；三苯基铋NSC 465|||NSC-465|||NSC465；NSC 465|||三苯基铋|||NSC-465|||NSC465
Triphenyl bismuth (NSC-465) is an additive for making biomedical resins visible on x-ray images and can be used as a radiopaque agent for orthopaedic bone cements.
价 格：￥电议型 号：T20112产 地：中国大陆
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T19112LSacubitril Enantiomer；LCZ 696杂质A2R,4S-Sacubitril|||ahu377 isomer 2；2R,4S-Sacubitril|||LCZ 696杂质A|||a
Sacubitril Enantiomer (ahu377 isomer 2) is the enantiomer of Sacubitril which is a neprilysin inhibitor.
价 格：￥电议型 号：T19112L产 地：中国大陆
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T191122R,4S-Sacubitril；LCZ 696杂质ASacubitril Enantiomer|||ahu377 isomer 2；LCZ 696杂质A|||Sacubitril Enantiome
2R,4S-Sacubitril (Sacubitril Enantiomer) is the impurity of Sacubitril which is a neprilysin inhibitor.
价 格：￥电议型 号：T19112产 地：中国大陆
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T191112R,4R-Sacubitril；化合物 T191112R,4R-Sacubitril
2R,4R-Sacubitril is the impurity of Sacubitril. Sacubitril is used in combination with valsartan for the treatment of patients with heart failure.
价 格：￥电议型 号：T19111产 地：中国大陆
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T18980Disperse Blue 148；化合物 T18980C.I. Disperse Blue 148|||C.I. 11124；C.I. Disperse Blue 148|||C.I. 11124
Disperse Blue 148 is the best high-temperature trichromatic blue azo dye.
价 格：￥电议型 号：T18980产 地：中国大陆
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T18112m-PEG-Tos (MW 2000)；化合物 T18112m-PEG-Tos (MW 2000)
m-PEG-Tos (MW 2000) is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T18112产 地：中国大陆
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T1811WH-4-023；化合物WH-4-023KIN112|||KIN001-112|||Dual LCK/SRC inhibitor；KIN112|||KIN001-112|||Dual LCK/SRC
WH-4-023 (Dual LCK/SRC inhibitor) is a potent and orally active Lck/Src inhibitor. It also potently inhibits SIK.
价 格：￥电议型 号：T1811产 地：中国大陆
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T1777Nintedanib；尼达尼布BIBF 1120|||Intedanib；BIBF 1120|||Intedanib|||尼达尼布
Nintedanib (Intedanib) is a triple vascular kinase inhibitor that inhibits VEGFR1, VEGFR2, and VEGFR3 (IC50=34/13/13 nM), FGFR1, FGFR2, and FGFR3 (IC50=69/37/108 nM), PDGFRα, and PDGFRβ (IC50=59/65 nM). Nintedanib has antitumor activity and inhibits tumor growth by inhibiting angiogenesis.
价 格：￥电议型 号：T1777产 地：中国大陆
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T17195UC-112；化合物UC-112UC-112
UC-112 is a novel potent IAP inhibitor and potently inhibits cell growth in two human melanoma and two human prostate cancer cell lines (IC50=0.7-3.4 uM).
价 格：￥电议型 号：T17195产 地：中国大陆
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T17112Todralazine；化合物 T17112Ecarazine；Ecarazine
Todralazine is an anti-hypertensive agent and acts as a β2AR blocker. It also has an antioxidant and free radical scavenging activity.
价 格：￥电议型 号：T17112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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T17007TC-Mps1-12化合物 T17007TCMps112|||TC-Mps-1-12|||TC Mps1 12
TC-Mps1-12 is an effective and selective inhibitor of monopolar spindle 1 (IC50: 6.4 nM) .
价 格：￥电议型 号：T17007产 地：中国大陆
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T16875SF1126；化合物 T16875SF1126
SF1126 is a relevant pan and dual first-in-class PI3K/BRD4 inhibitor. SF1126 is an RGDS-conjugated LY294002 prodrug, which is designed to exhibit increased solubility and bind to specific integrins within the tumor compartment.
价 格：￥电议型 号：T16875产 地：中国大陆
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T16756Risarestat；利沙司他CT 112；CT 112
Risarestat (CT-112) is a potent aldose reductase inhibitor and thyroid hormone receptor (TR) antagonist for the treatment of hypoglycemia.
价 格：￥电议型 号：T16756产 地：中国大陆
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T16704Quilseconazole；化合物 T16704VT-1129；VT-1129
Quilseconazole is an effective, orally active fungal Cyp51 inhibitor. it also binds tightly to cryptococcal CYP51 but weakly inhibits humans CYP450 enzymes.
价 格：￥电议型 号：T16704产 地：中国大陆
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T16112ML67-33化合物 T16112ML-67-33|||ML6733|||ML67 33
ML67-33 rapidly and reversibly affects K2P2.1 (TREK-1) (EC50s: 36.3 μM and 9.7 μM in cell-free and HEK293 cells, respectively). ML67-33 is a selective activator of temperature- and mechano-sensitive K2P channels.
价 格：￥电议型 号：T16112产 地：中国大陆
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T15748LG100754；化合物LG100754UVI 2112；UVI 2112
LG100754 (UVI 2112) is an insulin sensitizer that functions through RXR. LG100754 is an RXR dimer modulator. LG100754 acts as an RXR: RXR homodimer antagonist, but functions as an agonist towards RXR: PPARα and RXR: PPARγ heterodimers.
价 格：￥电议型 号：T15748产 地：中国大陆
