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T6976SB 239063inhibit,SB 239063,SB-239063,Inhibitor,Autophagy,p38 MAPK
SB239063 is a potent and selective p38 MAPKα/β inhibitor with IC50 of 44 nM, showing no activity against the γ- and δ-kinase isoforms.
价 格：￥电议型 号：T6976产 地：中国大陆
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T6676SofosbuvirPSI7977,inhibit,Inhibitor,HCV,PSI 7977,Hepatitis C virus,Sofosbuvir,GS-7977,GS7977
Sofosbuvir is a uridine monophosphate analog inhibitor of hepatitis C virus (HCV) polymerase NS5B that is used as an antiviral agent in the treatment of chronic hepatitis C.
价 格：￥电议型 号：T6676产 地：中国大陆
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TP1019LUrechistachykinin I acetate(149097-03-0 free base)Urechistachykinin I acetate(149097 03 0 free base)
Urechistachykinin I (Uru-TK I) acetate is an invertebrate kalinin-related peptide (TRPs) isolated from thylakoid nematodes.
价 格：￥电议型 号：TP1019L产 地：中国大陆
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T9799Serba-2Serba2,Serba 2
Serba-2 is an agonist of benzopyran selective estrogen receptor beta.
价 格：￥电议型 号：T9799产 地：中国大陆
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T9430Venadaparibinhibit,PARP,Venadaparib,IDX1197,Inhibitor,solid,IDX 1197,tumors,anticancer,poly ADP ribo
Venadaparib (IDX-1197) is a potent, selective and orally active PARP inhibitor with IC50s of 1.4 nM and 1.0 nM for PARP1 and PARP2, respectively. Venadaparib is insensitive to PARP-5. Venadaparib prevents the repair of DNA single-strand breaks (SSBs) and can be used in solid tumor research.
价 格：￥电议型 号：T9430产 地：中国大陆
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T9784Docosanedioic acid?Antibody-drug conjugates linkers,Docosanedioic acid,inhibit,Docosanedioic acid?,I
BEHENIC ACID is a alkyl-chain-based PROTAC linker. BEHENIC ACID is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T9784产 地：中国大陆
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T9954K-975YAP1,Cys359,pleural,TAZ,K 975,inhibit,K-975,Yes-associated protein,YAP,Inhibitor,antitumor,mali
K-975 is a highly selective, orally active TEAD inhibitor, effectively inhibiting protein-protein interactions between TEAD and YAP1/TAZ.
价 格：￥电议型 号：T9954产 地：中国大陆
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T15000Cort108297Cort108297,Cort-108297
Cort108297 is a specific antagonist of the glucocorticoid receptor with a high affinity for GRs (Ki: 0.45 nM).
价 格：￥电议型 号：T15000产 地：中国大陆
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T39979(S)-ErSO(S) ErSO,(S)ErSO
(S)-ErSO is an inactive dextrorotatory enantiomer of ErSO.
价 格：￥电议型 号：T39979产 地：中国大陆
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T7197Fadrozole(Rac)-FAD286,inhibit,Fadrozole,CGS 16949A,Inhibitor,Aromatase
Fadrozole is a nonsteroidal aromatase inhibitor with potential antineoplastic activity(IC50 : 6.4 nM)
价 格：￥电议型 号：T7197产 地：中国大陆
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T67854BAS 00489700
BAS 00489700 is a N-UTR interaction inhibitor. BAS 00489700 inhibits virus replication in cell culture.
价 格：￥电议型 号：T67854产 地：中国大陆
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T9729AGI-43192AGI 43192,AGI43192
AGI-43192 is a potent methionine adenosyltransferase 2A ( MAT2A ) inhibitor. AGI-43192 is a potent, but limited brain-penetrant compound. AGI-43192 has the potential for exploring the effects of SAM modulation in the central nervous system (CNS) and research of cancer disease [1].
价 格：￥电议型 号：T9729产 地：中国大陆
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T9011VU0155094VU0155094,Inhibitor,Metabotropic glutamate receptors,ML397,inhibit,mGluR
ML397 is a positive allosteric modulator with differential activity at the various group III mGluRs.
价 格：￥电议型 号：T9011产 地：中国大陆
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T6S1597Mulberroside AMulberroside A,Tumor Necrosis Factor Receptor,inhibit,TNF Receptor,Tyrosinase,TNFR,Inh
1. Mulberroside has nephroprotective, hypoglycemic, and antidiabetic effects. 2. Mulberroside A is a glycosylated stilbene of oxyresveratrol; thus, the deglycosylation of Mulberroside A resulted in enhanced inhibition of melanogenesis. 3. Mulberroside A has anti-inflammatory antiapoptotic effects. by decreasing the expressions of tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6 and inhibiting the activation of NALP3, caspase-1, and nuclear factor-κB and the phosphorylation of extra
价 格：￥电议型 号：T6S1597产 地：中国大陆
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T7502LPF 05089771Na+ channels,diabetic,inhibit,Inhibitor,neuropathy,Sodium Channel,Na channels,TTX-R,PF 05
PF-05089771 is a Selective inhibitor of Nav1.7 (IC50 = 11 nM) that interacts with the voltage-sensor domain of domain IV. It shows a slow onset of the block that is depolarization and concentration-dependent.
价 格：￥电议型 号：T7502L产 地：中国大陆
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TP1497LMast Cell Degranulating Peptide HR-2 acetateMast Cell Degranulating Peptide HR 2 acetate,Mast Cell D
Mast Cell Degranulating Peptide HR-2 acetate from giant hornet Vespa orientalis that has biological effects similar to mast cell degranulating peptide from bee venom.
价 格：￥电议型 号：TP1497L产 地：中国大陆
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T7412Tandospirone citrateSM3997,SM-3997,Tandospirone,Tandospirone citrate,Inhibitor,Serotonin Receptor,SM
Tandospirone citrate is a potent and selective 5-HT1A receptor partial agonist (Ki : 27 nM)
价 格：￥电议型 号：T7412产 地：中国大陆
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T9760IC 86621ATP,Buchwald-Hartwig amination,Inhibitor,IC-86621,IC86621,IC 86621,DSB,antitumor,inhibit,Apo
IC 86621 is a selective and reversible ATP-competitive inhibitor of DNA-PK with an IC50 of 120 nM. IC 86621 increases DNA double-strand break(DSB)-induced antitumor activity with an EC50 of 68 ?M for DNA-PK mediated cellular DSB repair.
价 格：￥电议型 号：T9760产 地：中国大陆
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TN2097Pomolic acidcancer,Inhibitor,inhibit,Randialic acid A,Pomolic acid,pentacyclic triterpene,ROS,Apopto
Pomolic acid has anti-cancer, anti-inflammatory and apoptotic activities, it can induce apoptosis in SK-OV-3 cells, which is mediated by the mitochondrial-mediated intrinsic and death receptor-induced extrinsic pathways.
价 格：￥电议型 号：TN2097产 地：中国大陆
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T39752CDK12-IN-2
CDK12-IN-2 is an effective and selective inhibitor of CDK12 with an IC50 of 52 nM, >100 μM, >10 μM and 16 μM for CDK12, CDK2, CDK7, and CDK9. CDK12-IN-2 can be used in studies about the function of CDK12.
价 格：￥电议型 号：T39752产 地：中国大陆
