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产品数：86101
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T17005FPR Agonist 43FPR Agonist 43
FPR Agonist 43 is a dual agonist of formyl peptide receptor 1 and formyl peptide receptor 2 (FPR2)/ALX.
价 格：￥电议型 号：T17005产 地：中国大陆
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T64375UNC?1021UNC?1021
UNC 1021 is a selective L3MBTL3 inhibitor (IC50 = 0.048 μM).
价 格：￥电议型 号：T64375产 地：中国大陆
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T6437CefoperazoneCefoperazone,inhibit,Inhibitor,Antibiotic,Bacterial
Cefoperazone binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. It can inhibit rMrp2-mediated [3H]E217βG uptake (IC50: 199 μM).
价 格：￥电议型 号：T6437产 地：中国大陆
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T22783FGIN-1-43FGIN143,FGIN 1 43
FGIN-1-43 is a potent and specific ligand for the mitochondrial DBI receptor.
价 格：￥电议型 号：T22783产 地：中国大陆
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TN2343Pseudojervine
Pseudojervine is derived from Veratrum nigrum L. Pseudojervine exhibits feeble inhibition activity against platelet aggregation.
价 格：￥电议型 号：TN2343产 地：中国大陆
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T643872-Nitrobenzoic acid
2-Nitrobenzoic acid is a antiproliferation agent. 2-Nitrobenzoic acid shows IC50 of 8.3 μM to jurkat cell line expressing T type calcium channel alpha 1H or its splice variant delta 25.
价 格：￥电议型 号：T64387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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T9943(E)-6-(4-methylbenzylidene)-5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid(E)6(4methylbenzyli
(E)-6-(4-methylbenzylidene)-5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid is a 2-?benzylidene tetrahydronaphthone derivative and can be used as a firefly luciferase inhibitor in kit.
价 格：￥电议型 号：T9943产 地：中国大陆
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T67844RBN-3143RBN3143
RBN-3143 is a potent and inhibitor of NAD+-competitive catalytic PARP14 (IC50= 4 nM). RBN-3143 inhibits ADP-ribosylation mediated by PARP14 and stabilizes PARP14 in cell lines. RBN-3143 exhibits research potential of lung inflammation.
价 格：￥电议型 号：T67844产 地：中国大陆
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T10436AZD4573AZD 4573,inhibit,CDK,AZD4573,AZD-4573,Inhibitor,Cyclin dependent kinase
AZD4573 is an effective and selective CDK9 inhibitor (IC50: <4 nM). It enables transient target engagement for the treatment of hematologic malignancies.
价 格：￥电议型 号：T10436产 地：中国大陆
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T64354Cystathionine-γ-lyase-IN-1
Cystathionine-γ-lyase-IN-1 is a selective inhibitor of cystathionine γ-lyase (CSE) enzyme (IC50= 6.3 μM).
价 格：￥电议型 号：T64354产 地：中国大陆
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TQ0159U-73343U-73343,Inhibitor,U73343,Phospholipase,inhibit
U 73343 is an inactive analog of U 73122 and can be used as a negative control. It dose-dependently inhibits acid secretion irrespective of the stimulant. It is a phospholipase C (PLC) and 5-LO (5-lipoxygenase) inhibitor with an IC50 of 1-2.1 μM for PLC.
价 格：￥电议型 号：TQ0159产 地：中国大陆
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T677434-Pyridinecarboxaldehyde, 2-(2-pyridinyl)hydrazone, [C(E)]-4Pyridinecarboxaldehyde,2(2pyridinyl)hydr
4-Pyridinecarboxaldehyde, 2-(2-pyridinyl)hydrazone, [C(E)]- is a ligand of mixed-ligand coordination polymer [Zn4(bdc)4(ppmh)2(H2O)]n.
价 格：￥电议型 号：T67743产 地：中国大陆
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T12262L1NPS ALX Compound 4a hydrochloride(1:1)NPSALXCompound4ahydrochloride(299433106Freebase)
NPS ALX Compound 4a hydrochloride(1:1) is a potent and selective 5-hydroxytryptamine6 (5-HT6) receptor antagonist, with an IC50 of 7.2 nM and a Ki of 0.2 nM.
价 格：￥电议型 号：T12262L1产 地：中国大陆
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T64337PF-04745637PF04745637,Inhibitor,bowel,TRPA1,disease,inhibit,respiratory,PF-04745637,Transient recept
PF-04745637 is a potent and selective TRPA1 antagonist with an IC50 of 17 nM[1].
价 格：￥电议型 号：T64337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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T6422Brimonidine TartrateUK-14304,UK14304,AGN190342,Brimonidine,Adrenergic Receptor,AGN-190342,AGN 190342
Brimonidine tartrate is a quinoxaline derivative and adrenergic α-2 receptor agonist (EC50: 0.45 nM) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension.
价 格：￥电议型 号：T6422产 地：中国大陆
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T94326-Bromo-2-naphthol6Bromo2naphthol,6 Bromo 2 naphthol
6-Bromo-2-naphthol is?an electrophilic carbene intermediate.
价 格：￥电议型 号：T9432产 地：中国大陆
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T5043Lentinanresponse,β-glucan,Shiitake,gastric,inhibit,cancer,Lentinan,modifier,Inhibitor,biological,mus
Lentinan, isolated and purified from a hot water extract of Lentinula edodes fruit bodies, is a fungal polysaccharide immunomodulator with anti-tumor effects.
价 格：￥电议型 号：T5043产 地：中国大陆
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T23439TC-N 1752TCN 1752,TC N 1752
TC-N 1752 is an orally active inhibitor of Nav1.7 channel with IC50 of 0.17 μM. TC-N 1752 shows analgesic activities.
价 格：￥电议型 号：T23439产 地：中国大陆
