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T17032Telratolimod；化合物TelratolimodMEDI9197|||3M-052；MEDI9197|||3M-052
Telratolimod (MEDI9197) is a toll-like receptors 7/8 agonist. It has an antitumor activity.
价 格：￥电议型 号：T17032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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T16976TAK-915；化合物 T16976TAK-915
TAK-915 is a potent, selective, and brain-penetrant phosphodiesterase 2A (PDE2A) inhibitor (IC50: 0.61 nM). TAK-915 is >4100-fold more selectivity for PDE2A than PDE1A.
价 格：￥电议型 号：T16976产 地：中国大陆
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T16972TA 0910 acid-type；化合物 T16972TA 0910 acid-type
TA 0910 acid-type is a metabolite of TA 0910. TA-0910 is a metabolically stable analog of thyrotropin-releasing hormone.
价 格：￥电议型 号：T16972产 地：中国大陆
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T16919Spirendolol；化合物 T16919S 32-468|||Substance 32468|||Li 32-468；S 32-468|||Substance 32468|||Li 32-468
Spirendolol is an antagonist of β adrenergic receptor.
价 格：￥电议型 号：T16919产 地：中国大陆
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T16918SPDP-PEG6-NHS ester；化合物 T16918SPDP-PEG6-NHS ester
SPDP-PEG6-NHS ester 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：T16918产 地：中国大陆
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T16917SPDP-PEG4-NHS ester；化合物 T16917SPDP-PEG4-NHS ester
SPDP-PEG4-NHS ester 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：T16917产 地：中国大陆
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T16916SPDP-PEG4-acid；化合物 T16916SPDP-PEG4-acid
SPDP-PEG4-acid 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：T16916产 地：中国大陆
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T16915SPDP-C6-NHS ester；化合物 T16915SPDP-C6-NHS ester
SPDP-C6-NHS ester is an alkyl/ether-based linker utilized in the synthesis of PROTACs[1].
价 格：￥电议型 号：T16915产 地：中国大陆
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T16914SP187；化合物SP187UV4|||MON-?DNJ；UV4|||MON-?DNJ
SP187 (MON-?DNJ) is a host-targeted iminosugar. It has anti-filovirus infection activity.SP187 is used for therapeutic use against influenza and dengue viruses.
价 格：￥电议型 号：T16914产 地：中国大陆
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T16913Sotirimod；索替莫德R850|||S-30594；R850|||S-30594
Sotirimod（R850） is a novel immunomodulator with antitumor and antiviral activity for the study of actinic keratoses.
价 格：￥电议型 号：T16913产 地：中国大陆
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T16912Sortin1化合物 T16912Sortin1|||Sortin-1
Sortin1, a chemical genetic-hit compound, specifically induces mislocalization of both soluble and membrane-associated vacuolar markers in plants and yeast.
价 格：￥电议型 号：T16912产 地：中国大陆
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T16911Sorivudine；索立夫定BV-araU；BV-araU|||索立夫定
Sorivudine (BV-araU) has antiviral activity against several viruses including varicella zoster virus, herpes simplex type 1 virus, and Epstein-Barr virus by interfering with viral DNA synthesis.
价 格：￥电议型 号：T16911产 地：中国大陆
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T16910Sorbinil；索比尼尔Sorbinil
Sorbinil is an Aldose reductase inhibitor. Sorbinil plays a therapeutic role in treating diabetes and diabetic complications decreases AR activity and inhibit the polyol pathway.
价 格：￥电议型 号：T16910产 地：中国大陆
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T16914-Formylbenzoic acid；对醛基苯甲酸Benzoic acid；对醛基苯甲酸|||Benzoic acid
4-Formylbenzoic acid (Benzoic acid) can be used as an intermediate for medicines, pesticides, and optical brighteners.
价 格：￥电议型 号：T1691产 地：中国大陆
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T16895SL910102；化合物 T16895SL910102
SL910102 is a nonpeptide angiotensin antagonist of the AT1 receptor.
价 格：￥电议型 号：T16895产 地：中国大陆
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T16891SKA-121；化合物 T16891SKA-121
SKA-121 is a selective KCa3.1 activator (EC50s: 109 nM and 4.4 μM for KCa3.1 and KCa2.3, respectively).
价 格：￥电议型 号：T16891产 地：中国大陆
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T16886Sinefungin；西奈芬净Adenosyl-Ornithine|||A-9145|||Antibiotic 32232RP；Adenosyl-Ornithine|||西奈芬净|||A-9145||
Sinefungin (Adenosyl-Ornithine) is an effective inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2´-)-methyltransferase, and viral multiplication. Sinefungin is a SET7/9 inhibitor and ameliorates renal fibrosis by inhibiting H3K4 methylation.
价 格：￥电议型 号：T16886产 地：中国大陆
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T16879LSHU 9119 acetate；化合物SHU 9119 acetateSHU 9119 acetate (168482-23-3 free base)；SHU 9119 acetate (16848
SHU 9119 acetate is a well-known antagonist of human melanocortin 3 and 4 (hMC3R, hMC4R) receptors and a partial hMC5R agonist. The IC50 values of human MC3R, MC4R and MC5R is 0.23, 0.06, and 0.09 nM respectively.
价 格：￥电议型 号：T16879L产 地：中国大陆
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T16879SHU 9119；化合物 T16879SHU 9119
SHU 9119 is an effective human melanocortin 3 and 4 receptors (MC3/4R) antagonist and a partial MC5R agonist (IC50: 0.23, 0.06, and 0.09 nM for human MC3R, MC4R and MC5R, respectively).
价 格：￥电议型 号：T16879产 地：中国大陆
