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T11218ε-?Viniferin；Epsilon-白藜芦醇脱氢二聚体epsilon-Viniferin；epsilon-Viniferin|||Epsilon-白藜芦醇脱氢二聚体
ε-?Viniferin (epsilon-Viniferin) a dimer of resveratrol, shows the inhibitory effects of epsilon-viniferin on human CYP1A1, CYP1A2, CYP1B1, CYP2A6, CYP2B6, CYP2E1, CYP3A4 and CYP4A activities.
价 格：￥电议型 号：T11218产 地：中国大陆
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T11212EPAC 5376753；化合物EPAC 53767535-{[5-(2,4-dichlorophenyl)furan-2-yl]methylidene}-2-thioxodihydropyrimid
EPAC 5376753 is an allosteric inhibitor of EPAC1 with an IC50 of 4 ?M in Swiss 3T3 cells.
价 格：￥电议型 号：T11212产 地：中国大陆
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T11210EP1013；化合物 T11210F1013；F1013
EP1013 is a broad-spectrum selective inhibitor of Caspase used in the study of type 1 diabetes.
价 格：￥电议型 号：T11210产 地：中国大陆
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T1121Podofilox鬼臼毒素鬼臼毒素|||Podophyllotoxin|||(+)-Shikonin
Podofilox ((+)-Shikonin) is a lignan (LIGNANS) found in PODOPHYLLIN resin from the roots of PODOPHYLLUM plants. It is a potent spindle poison, toxic if taken internally, and has been used as a cathartic. It is very irritating to skin and mucous membranes, has keratolytic actions, has been used to treat warts and keratoses, and may have antineoplastic properties, as do some of its congeners and derivatives.
价 格：￥电议型 号：T1121产 地：中国大陆
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T11206ent-Tadalafil；化合物 T11206ent-IC-351；ent-IC-351
ent-Tadalafil (ent-IC-351), compound (6S,12aS), is a inactive cis-enantiomer of compound (6R,12aS).
价 格：￥电议型 号：T11206产 地：中国大陆
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T11200Endoxifen (E-isomer)；N-去甲-4-羟基-三苯氧胺E-Endoxifen|||Endoxifen E-isomer；N-去甲-4-羟基-三苯氧胺|||E-Endoxifen|||E
Endoxifen E-isomer (E-Endoxifen) is the E-isomer of (Z)-Endoxifen. Endoxifen E-isomer has antiestrogenic effects.
价 格：￥电议型 号：T11200产 地：中国大陆
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T11198Endomorphin 2 TFA；内吗啡肽 2 三氟乙酸盐Endomorphin 2 TFA
Endomorphin 2 TFA, displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM. a high affinity, highly selective agonist of the μ-opioid receptor,
价 格：￥电议型 号：T11198产 地：中国大陆
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T11197Enclomiphene D4 hydrochloride；化合物 T11197(E)-Clomiphene D4 hydrochloride|||Enclomifene D4 hydrochlori
Enclomiphene D4 hydrochloride ((E)-Clomiphene D4 hydrochloride; trans-Clomiphene D4 hydrochloride; Enclomifene D4 hydrochloride) is a potent and orally active oestrogen receptor antagonist, with antioestrogenic property.Enclomiphene D4 hydrochloride ((E)-Clomiphene D4 hydrochloride; trans-Clomiphene D4 hydrochloride; Enclomifene D4 hydrochloride) is a deuterium labeled Enclomiphene.
价 格：￥电议型 号：T11197产 地：中国大陆
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T111959IFB-088 acetate；IFB-088 醋酸盐IFB-088 acetate
IFB-088 acetate, a benzyl guanidine derivative, is used to treat diseases and cancers associated with the PPP1R15A pathway and associated with protein misfolding stress, Examples include tau disease, synaptic riboprotein disease, polyglutamine and polyalanine diseases, leukodystrophy, cystic fibrosis, multiple sclerosis, lysosome storage disorders, amyloidosis diseases, inflammation, metabolic disorders, cardiovascular diseases, osteoporosis, neurological trauma, and more.
价 格：￥电议型 号：T111959产 地：中国大陆
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T11195Enantiomer of Sofosbuvir；化合物 T11195Enantiomer of Sofosbuvir
Sofosbuvir´s enantiomer, a variant of the prescription medication Sofosbuvir used for chronic hepatitis C treatment, currently lacks reported biological activity.
价 格：￥电议型 号：T11195产 地：中国大陆
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T1118LCefprozil；头孢丙烯Cefprozilum|||Cefprozilo|||Cefzil|||Brisoral|||Cefprozil anhydrous；Cefprozilum|||Cefpr
Cefprozil (Cefzil) is a novel cephalosporin antibiotic with antiviral activity for the study of immune system disorders.
价 格：￥电议型 号：T1118L产 地：中国大陆
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T11189Emtricitabine S-oxide；化合物 T11189Emtricitabine Degradant-III|||Emtricitabine sulfoxide；Emtricitabine
Emtricitabine, a potent nucleoside reverse transcriptase inhibitor, is employed for managing HIV infection. Emtricitabine S-oxide, also known as Emtricitabine sulfoxide, represents a significant degradation byproduct of Emtricitabine.
价 格：￥电议型 号：T11189产 地：中国大陆
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T11182EMD638683 S-Form；化合物 T11182EMD638683 S-Form
EMD638683 is a highly selective SGK1 inhibitor with IC50 of 3 μM. EMD638683 S-Form is the S-form of EMD638683.
价 格：￥电议型 号：T11182产 地：中国大陆
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T11181EMD638683 R-Form；化合物 T11181EMD638683 R-Form
EMD638683 is a highly selective SGK1 inhibitor with IC50 of 3 μM. EMD638683 R-Form is the R-form of EMD638683.
价 格：￥电议型 号：T11181产 地：中国大陆
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T1118Cefprozil monohydrate；头孢丙烯一水合物Cefprozil|||Cefprozil hydrate；Cefprozil|||头孢丙烯|||头孢丙烯一水合物|||Cefprozil
Cefprozil monohydrate (Cefprozil) is a second-generation cephalosporin-type antibiotic.
价 格：￥电议型 号：T1118产 地：中国大陆
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T11171eIF4A3-IN-2；化合物 T11171eIF4A3-IN-2
eIF4A3-IN-2 is a highly selective and noncompetitive eukaryotic initiation factor 4A-3 inhibitor with an IC50 of 110 nM.
价 格：￥电议型 号：T11171产 地：中国大陆
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T11170eIF4A3-IN-1；化合物 T11170eIF4A3-IN-1
eIF4A3-IN-1 is a selective eukaryotic initiation factor 4A3 (eIF4A3) inhibitor (IC50=0.26 μM; Kd=0.043 μM), which binds to a non-ATP binding site of eIF4A3 and shows significant cellular nonsense-mediated RNA decay (NMD) inhibition at 10 and 3 μM and can be as a probe for further study of eIF4A3, the exon junction complex (EJC), and NMD.
价 格：￥电议型 号：T11170产 地：中国大陆
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T11164EGFR mutant-IN-1；化合物 T11164EGFR mutant-IN-1
EGFR mutant- in-1, A 5-methylpyrimidopyridone derivative are effective selective EGFRL858R/T790M/C797S mutant inhibitors with IC50 of 27.5 nM, which significantly weakened EGFRWT effect.
价 格：￥电议型 号：T11164产 地：中国大陆
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T11163EGFR-IN-9；化合物EGFR-IN-9EGFR-IN-9
EGFR-IN-9 is a potent EGFR kinase inhibitor with IC50s of 7 nM, 28 nM for the wild type EGFR kinase and double mutant EGFR kinase (L858R/T790M). EGFR-IN-9 has antitumor activity.
价 格：￥电议型 号：T11163产 地：中国大陆
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T11162EGFR-IN-8；化合物EGFR-IN-8EGFR-IN-8
EGFR-IN-8, a dual inhibitor targeting both EGFR and c-Met, shows potential as a promising candidate for further development in treating EGFR TKI-resistant NSCLC.
价 格：￥电议型 号：T11162产 地：中国大陆
