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T39268Azido-PEG4-azideAzido-PEG4-azide
Azido-PEG4-azide is a PEG-based PROTAC linker that can be used to synthesize PROTACs.
价 格：￥电议型 号：T39268产 地：中国大陆
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T368663-DeazauridineNSC 126849；4-羟基-1-Β-D-呋喃核糖苷-2(1H)吡啶酮
3-Deazauridine is a structural analog of uridine that inhibits the biosynthesis of Cytidine-5´-Triphosphate by competitive inhibition of Cytidine Triphosphate synthetase which is considered to be the primary mode of action of this nucleoside analog.
价 格：￥电议型 号：T36866产 地：中国大陆
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T35827LPKCε Inhibitor Peptide acetatePKCε Inhibitor Peptide acetate(182683-50-7 Free base)
PKCε Inhibitor Peptide acetate is a selective PKCε inhibitor containing the site for its specific receptor for activated C kinase (RACK). PKCε Inhibitor Peptide acetate inhibits the translocation of PKCε, but not α-, β-, and δPKC.
价 格：￥电议型 号：T35827L产 地：中国大陆
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T3431Pardoprunox hydrochloride帕多芦诺盐酸盐；SLV-308 hydrochloride；DU-126891 hydrochloride
Pardoprunox hydrochloride is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist.
价 格：￥电议型 号：T3431产 地：中国大陆
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T3268Mildronate米屈肼；Meldonium；Kvaterin；Quaterin
Mildronate is an inhibitor of biosynthesis of L-carnitine by gamma-butyrobetaine (GBB) hydroxylase and as a competitive inhibitor of renal carnitine reabsorption.
价 格：￥电议型 号：T3268产 地：中国大陆
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T31587DY268DY 268；DY-268
DY-268 is a compound based on trisubstituted pyrazolamide without any FXR agonist activity and cytotoxicity and can be used as an effective FXR antagonist (IC50 = 7.5 nM).
价 格：￥电议型 号：T31587产 地：中国大陆
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T3007Spermine精胺；4,9-Diaza-1,12-dodecanediamine；NSC 268508；Neuridine；Musculamine；Gerontine
Spermine is a biogenic polyamine formed from spermidine. It is found in a wide variety of organisms and tissues and is an essential growth factor in some bacteria.
价 格：￥电议型 号：T3007产 地：中国大陆
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T2O2683L-Prolineproline；L-(-)-Proline；脯氨酸；L-脯氨酸
1. L-Proline is an osmoprotectant. 2. Proline and its derivatives are often used as asymmetric catalysts in organic reactions, as the CBS reduction and proline catalysed aldol condensation.
价 格：￥电议型 号：T2O2683产 地：中国大陆
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T2O2680Oxalic acid草酸；草酸；修酸;无水草酸；Aktisal；Aquisal；Ethanedioic acid；Wood bleach
Oxalic acid is a strong dicarboxylic acid occurring in many plants and vegetables. It is produced in the body by metabolism of glyoxylic acid or ascorbic acid. It is not metabolized but excreted in the urine. It is used as an analytical reagent and genera
价 格：￥电议型 号：T2O2680产 地：中国大陆
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T2689AZ3146AZ 3146
AZ3146 is a selective Mps1 inhibitor with IC50 of ~35 nM.
价 格：￥电议型 号：T2689产 地：中国大陆
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T26889BorofalanL-4-Boronophenylalanine
Borofalan echibits antineoplastic effects. Borofalan can be used in studies on recurrent or locally advanced head and neck cancer.
价 格：￥电议型 号：T26889产 地：中国大陆
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T2688LY310762LY310762 HCl
LY310762 is a 5-HT1D receptor antagonist with Ki of 249 nM.
价 格：￥电议型 号：T2688产 地：中国大陆
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T2687Omeprazole sulfideOmeprazole metabolite Omeprazole sulfide；Ufiprazole；奥美拉唑硫醚
Omeprazole sulfide is a metabolite of Omeprazole, which is a proton pump inhibitor.
价 格：￥电议型 号：T2687产 地：中国大陆
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T2686LEsomeprazole Sodium埃索美拉唑钠；(S)-Omeprazole sodium
Esomeprazole Sodium is the S-isomer of omeprazole with selective and irreversible proton pump inhibitor activity.Esomeprazole acts as an exosome inhibitor by blocking the exosome release via the inhibition of V-H+-ATPases
价 格：￥电议型 号：T2686L产 地：中国大陆
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T26869BMS-986122BMS986122；BMS 986122
BMS 986122 is a positive allosteric modulator of μ-opioid receptors that increases β-arrestin recruitment stimulated by endomorphin 1 in U2OS-OPRM1 human osteosarcoma cells expressing μ-opioid receptors (EC50 = 3 μM).
价 格：￥电议型 号：T26869产 地：中国大陆
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T2686Esomeprazole Magnesium埃索美拉唑镁；NEXIUM；(-)-Omeprazole magnesium；(S)-Omeprazole magnesium
Esomeprazole Magnesium is the S-isomer of omeprazole, can reduce gastric acid secretion with selective and irreversible proton pump inhibitor activity.Esomeprazole magnesium acts as an exosome inhibitor by blocking the exosome release via the inhibition
价 格：￥电议型 号：T2686产 地：中国大陆
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T26859BMS-8BMS8；BMS 8
BMS-8 is a novel inhibitor of the PD-1/PD-L1 interaction (IC50: 7.2 μM) by binding directly to PD-L1 and inducing the formation of PD-L1 homodimers.
价 格：￥电议型 号：T26859产 地：中国大陆
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T2685KU-55933ATM Kinase Inhibitor；KU55933
KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor.
价 格：￥电议型 号：T2685产 地：中国大陆
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T2684JNJ-1661010JNJ 1661010；Takeda-25；JNJ1661010
JNJ-1661010 is an effective and specific FAAH inhibitor (IC50: 10/ 12 nM for rat/human), shows >100-fold selectivity for FAAH-1 than FAAH-2.
价 格：￥电议型 号：T2684产 地：中国大陆
