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T32212Isoleucine orlistat, L-；化合物 T32212L-Isoleucine orlistat|||Orlistat related compound E；L-Isoleucine o
Isoleucine orlistat, L- is a bioactive chemical.
价 格：￥电议型 号：T32212产 地：中国大陆
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T31004Compound 8H；化合物 T31004Compound-8H|||Compound 8-H|||Compound 343；Compound-8H|||Compound 8-H|||Compoun
Compound 8H is an inducer of G2/M-phase cell cycle arrest and cell death in cancer cell lines.
价 格：￥电议型 号：T31004产 地：中国大陆
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T30786Cefepime related compound E；化合物 T30786Cefepime impurity E；Cefepime impurity E
Cefepime related compound E is an impurity of Cefepime and can be used in life science related experiments.
价 格：￥电议型 号：T30786产 地：中国大陆
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T29998Amlodipine besilate impurity F；化合物 T29998Amlodipine Dimethyl Ester|||Amlodipine USP Related Compound
Amlodipine besilate impurity F, also known as Amlodipine Dimethyl Ester, is a biochemical.
价 格：￥电议型 号：T29998产 地：中国大陆
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T294766-OH-BTA-0；化合物 T29476Pittsburgh Compound-B precursor|||11C-PiB Precursor；Pittsburgh Compound-B precu
6-OH-BTA-0 is the precursor for preparing 11C-PiB, which is a β-amyloid PET imaging tracer for Alzheimer´s disease diagnosis.
价 格：￥电议型 号：T29476产 地：中国大陆
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T29161STOCK2S-26016；化合物 T29161WNK IN B|||WNK-IN-B|||Compound B；WNK IN B|||WNK-IN-B|||Compound B
WNK-IN-B is an inhibitor of Wnk signalling. WNK-IN-B is a cell-permeable diaminoacridine derivative that targets the CCT domain of SPAK and OSR1 via reversible binding. WNK-IN-B selectively suppress hypotonic shock-induced WNK signaling pathway activation in mpkDCT and MOVAS (100 ?M) cultures without affecting p38 MAPK phosphorylation.
价 格：￥电议型 号：T29161产 地：中国大陆
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T28001MDK-6983；化合物MDK-6983MDK-6983|||Compound 6k|||Autophagy inhibitor 6k|||MDK6983；MDK-6983|||Compound 6k
MDK-6983 (MDK-6983) is an inhibitor of autophagy and disrupts the dynamics of actin cytoskeleton in human melanoma cells.
价 格：￥电议型 号：T28001产 地：中国大陆
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T27984MC-1353；化合物 T27984MC 1353|||Aroyl pyrrole hydroxy amide #8|||APHA Compound 8|||APHA-8；MC 1353|||Aroy
MC-1353 is a potent, selective inhibitor of HDAC class I.
价 格：￥电议型 号：T27984产 地：中国大陆
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T27757Kv1.5-IN-IIII；化合物 T27757Kv1.5INIIII|||Kv1.5INIV|||Compound IIII|||Kv1.5IN4|||Compound 4；Kv1.5INIIII|
Kv1.5-IN-IIII is a potent inhibitor of Kv1.5.
价 格：￥电议型 号：T27757产 地：中国大陆
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T27165Diazaborine；化合物 T27165Diazaborine compound 2b18|||Pkf 84.474|||Pkf 84474|||Pkf-84474|||SA-84474；Diaz
Diazaborine inhibits maturation of rRNAs for the large ribosomal subunit. Diazaborine blocks ribosome biogenesis by inhibiting the AAA-ATPase Drg1. Diazaborine treatment causes, within minutes, a rapid redistribution of the protein from the nucleolus to the periphery of the nucleus, which provides a possible explanation for the effect of diazaborine on rRNA processing.
价 格：￥电议型 号：T27165产 地：中国大陆
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T27058cp028；化合物 T27058cp 028|||Compound-028|||cp-028|||Compound028|||Compound 028；cp 028|||Compound-028|||
cp028 inhibits pre-mRNA splicing in vitro.
价 格：￥电议型 号：T27058产 地：中国大陆
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T26817Bim-BLK-A；化合物 T26817Bim Blocker A|||Compound A|||Bim BLK A|||BimBLKA；Bim Blocker A|||Compound A|||Bi
Bim-BLK-A efficiently blocks Bim-induced apoptosis after Bax is activated on the mitochondria. The cellular target of Bim-BLK-A was identified to be the succinate dehydrogenase subunit B (SDHB) protein of complex II of the mitochondrial electron transfer chain (ETC). Bim-BLK-A protects the integrity of the ETC and allows treated cells to continue to proliferate after apoptosis induction.
价 格：￥电议型 号：T26817产 地：中国大陆
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T25796Methotrexate 1-methyl ester；化合物 T25796Methotrexate related compound I|||Methotrexate alpha-methyl es
Methotrexate 1-methyl ester is an impurity of Methotrexate which is a folic acid antagonist. It´s used as an antineoplastic and antirheumatic.
价 格：￥电议型 号：T25796产 地：中国大陆
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T25153BIIK-0277；化合物 T25153Levalbuterol related compound E RS|||BIIK 0277；Levalbuterol related compound E R
BIIK-0277 (Levalbuterol Related Compound E) is a β2-adrenoceptor agonist, bronchodilator, and tocolytic.
价 格：￥电议型 号：T25153产 地：中国大陆
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T2503PAC-1；化合物PAC1Procaspase activating compound 1；Procaspase activating compound 1
PAC-1 (Procaspase activating compound 1) has been used in trials studying the treatment of Lymphoma, Melanoma, Solid Tumors, Breast Cancer, and Thoracic Cancers, among others.
价 格：￥电议型 号：T2503产 地：中国大陆
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T24994MreB Perturbing Compound A22 hydrochloride；化合物 T24994A22 hydrochloride|||MreB Perturbing Compound A2
A22 is an inhibitor of MreB, an actin-like bacterial protein, and has been proved to be an antibiotic adjuvant. A22 inhibition of MreB disrupts the bacterial actin cytoskeleton, which can cause an increase in cell permeability and altered transport.
价 格：￥电议型 号：T24994产 地：中国大陆
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T24455Methisazone；化合物 T24455Compound 33T57；Compound 33T57
Methisazone is an effective antiviral agent against poxviruses.
价 格：￥电议型 号：T24455产 地：中国大陆
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T23686AHR-activator-1023；化合物 T23686Branching Morphogenesis Modulator 1023|||Cpd 1023|||Compound 1023|||BMM
AHR-activator-1023 is the aryl hydrocarbon receptor activator. It is also a specific FGF2-induced branching morphogenesis modulator.
价 格：￥电议型 号：T23686产 地：中国大陆
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T226783,5-Bis(4-nitrophenoxy)benzoic acid；3,5-二(4-硝基苯氧基)苯甲酸Compound W；3,5-二(4-硝基苯氧基)苯甲酸|||Compound W
3,5-Bis(4-nitrophenoxy)benzoic acid (Compound W) is an inhibitor of γ-secretase. It also causes a decrease in the released levels of Aβ42 and notch-1 Aβ-like peptide 25 (Nβ25).
价 格：￥电议型 号：T22678产 地：中国大陆
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T22633CCT251545 analogue, Compound 51；化合物 T22633CCT251545 analogue, Compound 51
CCT251545 analog is a potent and selective CDK8/19 inhibitor (IC50: 5.1 nM and 5.6 nM, respectively). Mediator complex-associated kinases CDK8 and CDK19 are involved in the regulation of multiple transcription pathways. CDK8 plays as an oncogene in gastric and colorectal cancers through the activation of WNT signaling.
价 格：￥电议型 号：T22633产 地：中国大陆
