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T20588Tetrachlorvinphos；化合物 T20588Stirofos；Stirofos
Tetrachlorvinphos, an organophosphate cholinesterase inhibitor, is used as an insecticide. It has low toxicity to mammals.
价 格：￥电议型 号：T20588产 地：中国大陆
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T20178Metam-sodium；化合物 T20178Sodium methyldithiocarbamate|||Carbation|||Metham sodium|||Carbathione|||Carb
Metam-sodium is an organic sodium salt and organosulfur insecticide that appears as a yellow to light yellow-green solution with varying strengths of amine and sulfur odors. It can be used as a herbicide, insecticide, fungicide and pesticide.
价 格：￥电议型 号：T20178产 地：中国大陆
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T19868Thiambutosine；化合物 T19868SC 682|||SC-682|||SU-1906|||SU 1906|||SC682|||SU1906；SC 682|||SC-682|||SU-19
Thiambutosine was a candidate that is used for treatment of lepromatous leprosy.
价 格：￥电议型 号：T19868产 地：中国大陆
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T19728SPRC；化合物 T19728S-Propargyl-cysteine；S-Propargyl-cysteine
SPRC is a novel synthetic molecule exerting antioxidant effects via elevating the generation of endogenous H2S. SPRC activates Gp130-mediated STAT3 and prevents doxorubicin-induced cardiotoxicity.
价 格：￥电议型 号：T19728产 地：中国大陆
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T19568Sulfo-SMPB sodium；化合物 T19568Sulfo-SMPB sodium
Sulfo-SMPB sodium is a non-cleavable heterobifunctional chemical cross-linking reagent that combines N-hydroxysuccinimide ester and maleimide groups. This compound enables the covalent conjugation of molecules possessing amine and sulfhydryl functionalities.
价 格：￥电议型 号：T19568产 地：中国大陆
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T18718SPP-DM1；化合物 T18718SPP-DM1
SPP-DM1, a drug-linker conjugate for antibody-drug conjugates (ADC), demonstrates potent antitumor activity. It comprises DM1 (a potent microtubule-disrupting agent) connected through the ADC linker SPP[1].
价 格：￥电议型 号：T18718产 地：中国大陆
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T18708SPDP-C6-Gly-Leu-NHS ester；化合物 T18708SPDP-C6-Gly-Leu-NHS ester
SPDP-C6-Gly-Leu-NHS ester is a cleavable linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T18708产 地：中国大陆
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T18698SNPB-sulfo-Me；化合物 T18698SNPB-sulfo-Me
SNPB-sulfo-Me is a cleavable linker that is used for making antibody-drug conjugate (ADC).
价 格：￥电议型 号：T18698产 地：中国大陆
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T18678SC-VC-PAB-DM1；化合物 T18678SC-VC-PAB-DM1
SC-VC-PAB-DM1 is a drug-linker conjugate utilized in Antibody-Drug Conjugates (ADC), featuring DM1 (Mertansine, a tubulin inhibitor) linked through the SC-VC-PAB[1] ADC linker to deliver potent antitumor activity.
价 格：￥电议型 号：T18678产 地：中国大陆
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T17252SIM-688；化合物 SIM-688SIM688；SIM688
SIM-688 is a selective and orally active estrogen receptor inhibitor of NF-κB transcriptional activity (IC50 = 122 nM in HAECT-1 cells).
价 格：￥电议型 号：T17252产 地：中国大陆
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T17039Terbogrel；特波格雷BIBV 308SE；BIBV 308SE
Terbogrel is an oral thromboxane A2 receptor antagonist (IC50 is about 10 nM) and thromboxane A2 synthase inhibitor (IC50 is about 10 nM). Terbogrel is an antiplatelet compound that inhibits platelet aggregation and is a potential compound for the prevention of blood clots.
价 格：￥电议型 号：T17039产 地：中国大陆
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T16958Sulfo DBCO-PEG4-Maleimide；化合物 T16958Sulfo DBCO-PEG4-Maleimide
Sulfo DBCO-PEG4-Maleimide is a PEGylated derivative containing a maleimide group commonly employed as a linker for the synthesis of PROteolysis TAgeting Chimeras (PROTACs)[1].
价 格：￥电议型 号：T16958产 地：中国大陆
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T16936SS-208；化合物SS-208SS-208
SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.
价 格：￥电议型 号：T16936产 地：中国大陆
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T16930SR9238；化合物SR9238SR9238
SR9238 is a synthetic agonist of liver X receptor inverse (IC50s: 214 nM and 43 nM for LXRα and LXRβ, respectively).
价 格：￥电议型 号：T16930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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T16878SHP836；化合物 T16878SHP836
SHP836 is an inhibitor of SHP2 allosteric (IC50: 12 μM for the full-length SHP2).
价 格：￥电议型 号：T16878产 地：中国大陆
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T16848SB-218078；化合物 T16848SB-218078
SB-218078 is less potently inhibits Cdc2 (IC50: 250 nM) and PKC (IC50: 1000 nM). SB-218078 is a potent, ATP-competitive, and cell-permeable checkpoint kinase 1 inhibitor that inhibits Chk1 phosphorylation of cdc25C (IC50: 15 nM).
价 格：￥电议型 号：T16848产 地：中国大陆
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T16828S-Acetyl-PEG8-OH；化合物 T16828S-Acetyl-PEG8-OH
S-Acetyl-PEG8-OH 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：T16828产 地：中国大陆
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T16818S-8921；化合物 T16818S-8921
S-8921 is an inhibitor of ileal Na+/bile acid cotransporter.
价 格：￥电议型 号：T16818产 地：中国大陆
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T16408Osanetant；化合物 T16408SR142801；SR142801
Osanetant produces anxiolytic- and antidepressant-like effects. Osanetant is a selective NK3 receptor antagonist. It is researched for schizophrenia.
价 格：￥电议型 号：T16408产 地：中国大陆
