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T8598CHEMBL241987CHEMBL241987,CHEMBL-241987
CHEMBL241987 targets the Adenosine receptor A3 (human)
价 格：￥电议型 号：T8598产 地：中国大陆
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T4684ML241 hydrochloride
ML241 is a potent and selective inhibitors of p97 ATPase.ML241 inhibits degradation of a p97-dependent but not a p97-independent proteasome substrate in a dual-reporter cell line. ML241 may be a novel agent for the chemotherapy of cancer, and provide a ra
价 格：￥电议型 号：T4684产 地：中国大陆
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T3961CYM-5541ML249；CYM 5541；CID-17253208
CYM-5541 is a selective and allosteric S1P3 receptor agonist.
价 格：￥电议型 号：T3961产 地：中国大陆
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T23860CAY10444BML-241；CAY 10444；BML241；BML 241；CAY-10444
CAY10444 is an S1P3 specific antagonist.
价 格：￥电议型 号：T23860产 地：中国大陆
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T12006MetarrestinML246
Metarrestin is a first-in-class perinucleolar compartment inhibitor with a favorable PK profile, which effectively suppresses metastasis. Metarrestin disrupts the nucleolar structure and inhibits RNA polymerase (Pol) I transcription, at least in part by i
价 格：￥电议型 号：T12006产 地：中国大陆
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T1008624-Hydroxycholesterol24-Hydroxycholesterol
24-Hydroxycholesterol is a natural sterol, which serves as a positive allosteric modulator of NMDA receptors, and a potent activator of the transcription factors LXR.
价 格：￥电议型 号：T10086产 地：美洲
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T1008824R-Calcipotriol24R-Calcipotriol,PRI 2202,
24R-Calcipotriol(PRI 2202) is an impurity of Calcipotriol which is a ligand of VDR-like receptors.
价 格：￥电议型 号：T10088产 地：美洲
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T12006MetarrestinMetarrestin,ML246,
Metarrestin is a first-in-class perinucleolar compartment inhibitor with a favorable PK profile, which effectively suppresses metastasis.?Metarrestin disrupts the nucleolar structure and inhibits RNA polymerase (Pol) I transcription, at least in part by i
价 格：￥电议型 号：T12006产 地：美洲
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T4684ML241 hydrochlorideML241 hydrochloride
ML241 is a potent and selective inhibitors of p97 ATPase.ML241 inhibits degradation of a p97-dependent but not a p97-independent proteasome substrate in a dual-reporter cell line. ML241 may be a novel agent for the chemotherapy of cancer, and provide a ra
价 格：￥电议型 号：T4684产 地：美洲
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T8598CHEMBL241987；化合物CHEMBL2419872-PHENYL-2,5-DIHYDRO-4H-PYRAZOLO[3,4-C]QUINOLIN-4-ONE；2-PHENYL-2,5-DIHYD
CHEMBL241987 targets the Adenosine receptor A3 (human)
价 格：￥电议型 号：T8598产 地：中国大陆
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T78166MEL24；化合物 MEL24MEL24
MEL24, an Mdm2 E3 ligase inhibitor, diminishes cell viability and enhances sensitivity to DNA-damaging agents in a p53-dependent manner, suggesting its potential for in vitro antitumor research [1].
价 格：￥电议型 号：T78166产 地：中国大陆
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T73523OUL245；化合物 OUL245OUL245
OUL245, a 7-Hydroxy derivative, selectively inhibits PARP2 with an IC50 of 44 nM. Additionally, it exhibits inhibition against other PARP and TNKS enzymes, displaying IC50 values ranging from 2.9 to 8.8 μM.
价 格：￥电议型 号：T73523产 地：中国大陆
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T7175624(S),25-Epoxycholesterol；化合物 24(S),25-Epoxycholesterol24(S),25-Epoxycholesterol
24(S),25-Epoxycholesterol is an oxysterol agonist of the liver X receptor.
价 格：￥电议型 号：T71756产 地：中国大陆
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T4684ML241 hydrochloride；化合物ML241 hydrochlorideML241 hydrochloride
ML241 is a potent and selective inhibitors of p97 ATPase.ML241 inhibits degradation of a p97-dependent but not a p97-independent proteasome substrate in a dual-reporter cell line. ML241 may be a novel agent for the chemotherapy of cancer, and provide a rationale for developing pathway-specific p97 inhibitors.
价 格：￥电议型 号：T4684产 地：中国大陆
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T3961CYM-5541；化合物CYM 5541CYM 5541|||ML249|||CID-17253208；CYM 5541|||ML249|||CID-17253208
CYM-5541 (ML249) is a selective and allosteric S1P3 receptor agonist.
价 格：￥电议型 号：T3961产 地：中国大陆
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T3535ML240；化合物ML240ML240
ML240 is a selective, ATP-competitive p97 inhibitor.
价 格：￥电议型 号：T3535产 地：中国大陆
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T3164ML241；化合物ML241ML241
ML241 is a potent and selective inhibitors of p97 ATPase.
价 格：￥电议型 号：T3164产 地：中国大陆
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T25254CL 242817；化合物 T25254CL242817|||CL-242817；CL242817|||CL-242817
CL 242817 is an inhibitor of angiotensin converting enzyme (ACE).
价 格：￥电议型 号：T25254产 地：中国大陆
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T23860CAY10444；化合物 T23860BML-241|||CAY 10444|||CAY-10444|||BML241|||BML 241；BML-241|||CAY 10444|||CAY-1044
CAY10444 is an S1P3 specific antagonist.
价 格：￥电议型 号：T23860产 地：中国大陆
