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T83242-((9R,10S,11R,15S)-12,14-dioxo-9,10-dih2 ((9R,10S,11R,15S) 12,14 dioxo 9,10 dih,2((9R,10S,11R,15S)1
2-((9R,10S,11R,15S)-12,14-dioxo-9,10-dih is a chemical compound.
价 格：￥电议型 号：T8324产 地：中国大陆
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T6681STF-083010STF 083010,STF-083010,Inositol requiring enzyme 1,Inhibitor,inhibit,IRE1
STF-083010 is a selective inhibitor of the IRE1α endonuclease.
价 格：￥电议型 号：T6681产 地：中国大陆
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T12848SB-657510SB-657510
SB-657510 is a selective antagonist of urotensin II (UII) receptor (UT).
价 格：￥电议型 号：T12848产 地：美洲
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T83242-((9R,10S,11R,15S)-12,14-dioxo-9,10-dih；化合物T83242-((9R,10S,11R,15S)-12,14-dioxo-9,10-dih
Compound 8 can bind to GID1， By the results of the in vitro binding assays, chemical 8 showed greater effects than did 67D in an in vivo experimental system.
价 格：￥电议型 号：T8324产 地：中国大陆
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T81185SDH-IN-10；化合物 SDH-IN-10SDH-IN-10
SDH-IN-10 is a potent inhibitor of succinate dehydrogenase (SDHI) that exhibits antifungal activity [1].
价 格：￥电议型 号：T81185产 地：中国大陆
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T79515SARS-CoV-2 Mpro-IN-10；化合物 SARS-CoV-2 Mpro-IN-10SARS-CoV-2 Mpro-IN-10
SARS-CoV-2 Mpro-IN-10 (27h) is a potent inhibitor of the Mpro enzyme, exhibiting IC50 and EC50 values of 10.9 nM and 43.6 nM, respectively. It is utilized in research focused on the SARS-CoV-2 virus [1].
价 格：￥电议型 号：T79515产 地：中国大陆
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T72312SARS-CoV-2 3CLpro-IN-10；化合物 SARS-CoV-2 3CLpro-IN-10SARS-CoV-2 3CLpro-IN-10
SARS-CoV-2 3CLpro-IN-10(5d) is a potent inhibitor of the SARS-CoV-2 3CL protease, exhibiting an IC50 value of 190 nM, and demonstrates varied efficiency against other coronaviruses with IC50 values of 790 nM for SARS-CoV-1 and 70 nM for MERS-CoV, indicating broad-spectrum antiviral activity.
价 格：￥电议型 号：T72312产 地：中国大陆
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T71864SJ572710；化合物 SJ572710SJ572710
SJ572710 is an inhibitor of the disordered protein, p27(Kip1).
价 格：￥电议型 号：T71864产 地：中国大陆
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T71454Sas 1310；化合物 Sas 1310Sas 1310
Sas 1310 is a diltiazem derivative that acts as a calcium antagonist.
价 格：￥电议型 号：T71454产 地：中国大陆
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T70679Spr 210；化合物 Spr 210Spr 210
Spr 210 is an aldose reductase (AR) inhibitor with potential uses as a therapeutic agent for preventing and improving some diabetic complications.
价 格：￥电议型 号：T70679产 地：中国大陆
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T6681STF-083010；化合物STF083010STF083010；STF083010
STF-083010 is a selective inhibitor of the IRE1α endonuclease.
价 格：￥电议型 号：T6681产 地：中国大陆
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T66656(R)-Methyl 4-((3R,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopent
(R)-Methyl 4-((3R,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate is a useful organic compound for research related to life sciences. The catalog number is T66656 and the CAS number is 10538-59-7.
价 格：￥电议型 号：T66656产 地：中国大陆
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T66136(R)-Methyl 4-((3R,5S,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-
(R)-Methyl 4-((3R,5S,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate is a useful organic compound for research related to life sciences. The catalog number is T66136 and the CAS number is 10538-65-5.
价 格：￥电议型 号：T66136产 地：中国大陆
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T64990(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-10,13-Dimethyl-2,16-di(piperidin-1-yl)hexadecahydro-1H-cyclopen
(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-10,13-Dimethyl-2,16-di(piperidin-1-yl)hexadecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol is a useful organic compound for research related to life sciences. The catalog number is T64990 and the CAS number is 13522-16-2.
价 格：￥电议型 号：T64990产 地：中国大陆
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T64669(R)-4-((3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-Trihydroxy-7,10,13-trimethylhexadecahydro-1H-cycl
(R)-4-((3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-Trihydroxy-7,10,13-trimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid is a useful organic compound for research related to life sciences and the catalog number is T64669.
价 格：￥电议型 号：T64669产 地：中国大陆
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T63457STING agonist-10；化合物 STING agonist-10STING agonist-10
STING agonist-10 is a potent activator of the STING small molecule cyclic urea class (EC50: 2600 nM).STING activation is a highly promising immunotherapy.
价 格：￥电议型 号：T63457产 地：中国大陆
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T63102SIRT2-IN-10；化合物 SIRT2-IN-10SIRT2-IN-10
SIRT2-IN-10 (Compound 12) is a potent inhibitor of SIRT2 (IC50: 1.3 μM), which can be used in the study of cancer and neurodegenerative diseases.
价 格：￥电议型 号：T63102产 地：中国大陆
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T62712SOS1-IN-10；化合物 SOS1-IN-10SOS1-IN-10
SOS1-IN-10 is a potent inhibitor of SOS1 that acts on KRAS G12C-SOS1 (IC50: 13 nM).
价 格：￥电议型 号：T62712产 地：中国大陆
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T62253S-HP210；化合物 S-HP210S-HP210
S-HP210 is a selective and potent glucocorticoid receptor (GR) modulator that inhibits NF-κB transcription (IC50: 1.92 μM). S-HP210 is not toxic to mouse fibroblasts at effective doses of 3T3.
价 格：￥电议型 号：T62253产 地：中国大陆
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T61485S07-2010；化合物 S07-2010S07-2010
S07-2010 is a potent pan-AKR1C inhibitor, effectively inhibiting AKR1C3, AKR1C4, AKR1C1, and AKR1C2 with IC50 values of 0.19, 0.36, 0.47, and 0.73 μM, respectively. This compound induces apoptosis in A549/DDP cells and enhances the cytotoxicity of chemotherapeutic agents in drug-resistant cells, making it a viable option for combating drug resistance. Furthermore, S07-2010 significantly inhibits the proliferation of drug-resistant cells [1].
价 格：￥电议型 号：T61485产 地：中国大陆
