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产品数：86101
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T12115MSC2360844；化合物MSC2360844MSC2360844
MSC2360844 is a potent, orally active and selective inhibitor of PI3Kδ(IC50 of 145 nM).
价 格：￥电议型 号：T12115产 地：中国大陆
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T121011TLC1566-0618；化合物TLC1566-0618TLC1566-0618
TLC1566-0618 shows antitumor activity and targets stat.
价 格：￥电议型 号：T121011产 地：中国大陆
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T120656N004-0015；化合物 N004-0015N004-0015
Plasmodium falciparum, EC50: 7.21 nM
价 格：￥电议型 号：T120656产 地：中国大陆
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T12015Methyl homoveratrate；3,4-二甲氧基苯乙酸甲酯Methyl homoveratrate
Methyl homoveratrate, a McN5691 (RWJ-26240) metabolite detected in vivo in plasma, urine, and fecal extracts, functions as a voltage-sensitive calcium channel blocker.
价 格：￥电议型 号：T12015产 地：中国大陆
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T11922LY 254155；化合物 T11922LY 254155
LY 254155, an antifolate,binds to mFBP and inhibits hGARFT with Kis of 1.7±0.1 and 2.1±0.2 nM, respectively.
价 格：￥电议型 号：T11922产 地：中国大陆
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T11915LY88074；化合物LY88074LY88074
LY88074 is a raloxifene analog in which the basic side chain has been removed. LY88074 is an agonist of ERβ (EC50 = 232 nM).This compound stimulates uterine cell proliferation.
价 格：￥电议型 号：T11915产 地：中国大陆
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T11912LY3154207；化合物 T11912LY3154207
LY3154207 is a subtype selective, potent, and orally available human dopamine D1 receptor positive allosteric modulator (PAM) with minimal allosteric agonist activity (EC50=3 nM).
价 格：￥电议型 号：T11912产 地：中国大陆
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T11905LY-411575 isomer 3；化合物 T11905LY-411575 isomer 3
LY-411575 isomer 3 is a potent γ-secretase inhibitor. LY-411575 isomer 3 is an isomer of LY411575.
价 格：￥电议型 号：T11905产 地：中国大陆
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T11904LY-411575 isomer 2；化合物 T11904LY-411575 isomer 2
LY-411575 isomer 2 is a potent γ-secretase inhibitor. LY-411575 isomer 2 is an isomer of LY411575.
价 格：￥电议型 号：T11904产 地：中国大陆
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T11903LY-411575 isomer 1；化合物 T11903LY-411575 isomer 1
LY-411575 isomer 1 is a potent γ-secretase inhibitor. LY-411575 isomer 1 is an isomer of LY411575.
价 格：￥电议型 号：T11903产 地：中国大陆
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T11822LAU159；化合物LAU159LAU159
LAU159 is a functionally selective positive α1β3 GABA(A) receptor modulator(EC50 : 2.2 μM).
价 格：￥电议型 号：T11822产 地：中国大陆
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T11815Lanopepden；拉诺普登GSK 1322322|||GSK-1322322B|||GSK-1322322J；GSK 1322322|||GSK-1322322B|||GSK-1322322J
Lanopepden (GSK 1322322) is a potent peptide deformylase inhibitor of Staphylococcus aureus, inhibiting ATCC 29213 and ATCC 25923 strains, and can be used in the study of pneumonia, dermatological and infectious diseases.
价 格：￥电议型 号：T11815产 地：中国大陆
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T11814Lamivudine 13C,15N2；化合物 T11814Lamivudine 13C,15N2
Lamivudine 13C,15N2, an impurity of Lamivudine (BCH-189), functions as an inhibitor of both HIV-1/2 reverse transcriptase and hepatitis B virus reverse transcriptase, classifying it as a nucleoside reverse transcriptase inhibitor (NRTIs).
价 格：￥电议型 号：T11814产 地：中国大陆
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T11769KRAS G12C inhibitor 15；化合物 T11769KRAS G12C inhibitor 15
KRAS G12C inhibitor 15 is a potent KRAS G12C inhibitor .
价 格：￥电议型 号：T11769产 地：中国大陆
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T11759Kif15-IN-2；化合物 T11759Kif15-IN-2
Kif15-IN-2 is used for the research of cellular proliferative diseases. Kif15-IN-2 is an inhibitor of the mitotic kinesin Kif15.
价 格：￥电议型 号：T11759产 地：中国大陆
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T11715JH-LPH-28；化合物 T11715JH-LPH-28
JH-LPH-28, a sulfonyl piperazine analog, is a potent inhibitor of UDP-2,3-diacylglucosamine pyrophosphate hydrolase LpxH, exhibiting exceptional antibiotic activity with a minimum inhibitory concentration (MIC) value of 0.83 μg/mL.
价 格：￥电议型 号：T11715产 地：中国大陆
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T11700J-2156；化合物 T11700J-2156
The ED50 of J-2156 in rats for the relief of mechanical allodynia and mechanical hyperalgesia in the ipsilateral hindpaws was 3.7 and 8.0 mg/kg, respectively. J-2156 is a high potent, selective somatostatin receptor type 4 (SST4 receptor) agonist with IC50s of 0.05 nM and 0.07 nM for human and rat SST4 receptors, respectively.
价 格：￥电议型 号：T11700产 地：中国大陆
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T11669IR415；化合物IR415IR415
IR415 selectively interacts with Hepatitis B virus X protein (HBx, Kd = 2 nM) and blocks HBV-mediated RNAi suppression, reverses the inhibitory effect of HBx protein on the activity of the dicer endoribonuclease. IR415 is a potent anti-HBV agent and inhibits HBV replication by blocking the HBx activity.
价 格：￥电议型 号：T11669产 地：中国大陆
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T11657INH154；化合物INH154INH154
INH154 is a potent Nek2 and Hec1 binding (INH) inhibitor with IC50s of 120 nM in MB468 cells and 200 nM in Hela cells for INH.
价 格：￥电议型 号：T11657产 地：中国大陆
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T11634IL-15-IN-1；化合物IL-15-IN-1IL-15-IN-1
IL-15-IN-1 is a selective and potent Interleukin 15 (IL-15) inhibitor, inhibiting the proliferation of IL-15-dependent cells (IC50: 0.8 μM).
价 格：￥电议型 号：T11634产 地：中国大陆
