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T16974TAK-243；化合物TAK-243MLN7243；MLN7243
TAK-243 (MLN7243) is a selective inhibitor of the ubiquitin-activating enzyme UAE (IC50=1 nM). TAK-243 blocks ubiquitin binding and disrupts mono-ubiquitin signaling as well as overall protein ubiquitination. TAK-243 exhibits antitumor activity and promotes apoptosis.
价 格：￥电议型 号：T16974产 地：中国大陆
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T16973TAK-220；化合物 T16973TAK-220
TAK-220 is a selective and orally bioavailable CCR5 antagonist (IC50s: 3.5 nM and 1.4 nM for inhibition on the binding of RANTES and MIP-1α to CCR5, respectively).
价 格：￥电议型 号：T16973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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T16971t-Boc-Aminooxy-PEG7-methane；化合物 T16971t-Boc-Aminooxy-PEG7-methane
t-Boc-Aminooxy-PEG7-methane is a polyethylene glycol (PEG)-based linker, which finds application in the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T16971产 地：中国大陆
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T16970t-Boc-aminooxy-PEG6-propargyl；化合物 T16970t-Boc-aminooxy-PEG6-propargyl
t-Boc-aminooxy-PEG6-propargyl is a PEG-based PROTAC linker utilized for PROTAC synthesis[1].
价 格：￥电议型 号：T16970产 地：中国大陆
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T1697debutylbupivacaine；N-(2’,6’-二甲苯基)-2-哌啶甲酰胺debutylbupivacaine
Debutylbupivacaine is the intermediate of ropivacaine hydrochloride and bupivacaine.
价 格：￥电议型 号：T1697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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T16897SM-6586；化合物SM-6586SM-6586
SM-6586 is a potent calcium channel antagonist with inhibitory effects on Na+/H+ and Na+/Ca2+ exchange channels, and can be used in the study of cerebrovascular disease and hypertension, among other diseases.
价 格：￥电议型 号：T16897产 地：中国大陆
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T16866SDZ281-977；化合物 T16866SDZ-LAP 977；SDZ-LAP 977
SDZ 281-977 is a derivative of Lavendustin A which is the EGF receptor tyrosine kinase inhibitor.
价 格：￥电议型 号：T16866产 地：中国大陆
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T16797RPR104632；化合物RPR104632RPR104632
RPR104632 is a novel and potent antagonist located at the NMDA glycine site with neuroprotective activity.
价 格：￥电议型 号：T16797产 地：中国大陆
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T16740RH1；化合物 RH1NSC 697726；NSC 697726
RH1 (NSC 697726) is a bioreductive anticancer compound that exhibits dose-dependent biphasic effects in vitro, inducing apoptosis at higher doses and senescence at lower doses.
价 格：￥电议型 号：T16740产 地：中国大陆
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T16734LResorufin sodium salt；试卤灵钠盐NSC 12097 sodium salt；试卤灵钠盐|||NSC 12097 sodium salt
Resorufin sodium salt (NSC-12097 sodium salt) is a fluorescent pink dye.
价 格：￥电议型 号：T16734L产 地：中国大陆
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T16734Resorufin；试卤灵NSC 12097；NSC 12097|||试卤灵
Resorufin (NSC-12097) (NSC-12097) is a highly fluorescent pink dye.
价 格：￥电议型 号：T16734产 地：中国大陆
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T16724Razuprotafib；化合物RazuprotafibAKB-9778；AKB-9778
Razuprotafib (AKB-9778) is a protein tyrosine phosphatase ? (HPTP?) inhibitor (IC50: 50 nM). Razuprotafib is effective for the activation of Tie-2 and is protective against acute kidney injury.
价 格：￥电议型 号：T16724产 地：中国大陆
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T16697Pyronaridine tetraphosphate；磷酸咯萘啶Pyronaridine tetraphosphate
Pyronaridine tetraphosphate is an orally active, mannitol-containing inhibitor of DNA topoisomerase 2 and erythrocyte cytokine with antimalarial and antitumour activity.Pyronaridine tetraphosphate treats P. falciparum and Echinococcus granulosus infections. Pyronaridine tetraphosphate treats P. falciparum and Echinococcus granulosus infections and attenuates Ebola virus transmission.
价 格：￥电议型 号：T16697产 地：中国大陆
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T16679Belzutifan；化合物BelzutifanPT2977|||MK-6482；PT2977|||MK-6482
Belzutifan (MK-6482) is a potential treatment for clear cell renal cell carcinoma (ccRCC). Belzutifan is an orally active and selective HIF-2α inhibitor (IC50: 9 nM). Belzutifan , as a second-generation HIF-2α inhibitor, increases potency and improves pharmacokinetic profile.
价 格：￥电议型 号：T16679产 地：中国大陆
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T16676PSI-697；化合物 T16676P-Selectin Inhibitor；P-Selectin Inhibitor
PSI-697 is an inhibitor of oral P-selectin (IC50: 125 μM).
价 格：￥电议型 号：T16676产 地：中国大陆
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T16597Propargyl-PEG2-acid；化合物 T16597Propargyl-PEG2-acid
Propargyl-PEG2-acid is a non-cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T16597产 地：中国大陆
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T16569Praliciguat；化合物PraliciguatIW-1973；IW-1973
Praliciguat (IW-1973) stimulates sGC in HEK-293 cells (EC50: 197 nM). Praliciguat is an effective and orally active soluble guanylate cyclase stimulator. It also enhances NO signaling and acts as a vasodilator.
价 格：￥电议型 号：T16569产 地：中国大陆
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T16497PF 1022A化合物 T16497PF 1022A
PF 1022A is an N-methylated cyclooctadepsipeptides with strong anthelmintic properties. It also acts as an ionosphere.
价 格：￥电议型 号：T16497产 地：中国大陆
