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T14120ACT-709478；化合物 T14120ACT-709478
ACT-709478 is a potent, selective T-type calcium channel blocker that is orally active and capable of penetrating the brain. It is currently utilized in research focusing on generalized epilepsies[1].
价 格：￥电议型 号：T14120产 地：中国大陆
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T1412Loxapine succinate；琥珀酸洛沙平Daxolin|||Loxapac|||Cloxazepin|||Loxapine succinate salt；Daxolin|||Loxapac|
Loxapine succinate (Loxapac), a D2DR and D4DR inhibitor, is utilized in schizophrenia.
价 格：￥电议型 号：T1412产 地：中国大陆
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T14119ACT-678689；化合物ACT-678689Compound Example 1.53.4；Compound Example 1.53.4
ACT-678689 (Compound Example 1.53.4) (Compound Example 1.53.4) is a tryptophan hydroxylase (TPH) inhibitor with an IC50 of 8 nM[1].
价 格：￥电议型 号：T14119产 地：中国大陆
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T14118Acridine Orange hydrochloride吖啶橙吖啶橙|||3,6-双(二甲基氨基)吖啶
Acridine Orange hydrochloride is a fluorescent dye of cell-permeable. It binds to nucleic acids, resulting in an altered spectral emission.It is used as a supravital stain and in fluorescence cytochemistry. It may cause mutations in microorganisms.
价 格：￥电议型 号：T14118产 地：中国大陆
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T14117Acridine Orange 10-Nonyl Bromide10-壬基溴代吖啶橙Nonylacridine orange|||10-壬基溴代吖啶橙
Acridine Orange 10-Nonyl Bromide is a cardiolipin fluorescent probe (λex: 489 nm, λem: 525 nm).
价 格：￥电议型 号：T14117产 地：中国大陆
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T14116ACP-105；化合物ACP-105ACP-105
ACP-105 is a novel and potent nonsteroidal selective androgen receptor modulator (SARM) with partial agonist activity relative to the natural androgen testosterone.
价 格：￥电议型 号：T14116产 地：中国大陆
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T14115Acoziborole；化合物 T14115SCYX-7158|||AN5568；SCYX-7158|||AN5568
Acoziborole (SCYX-7158), a derivative of benzoxaborole, is a safe, effective and structurally novel antigen-worm agent for human African trypanosomiasis (HAT) studies. The MIC value of Acoziborole for T. b. brucei S427 was 0.6 ?g/mL.
价 格：￥电议型 号：T14115产 地：中国大陆
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T14114Acivicin；阿西维辛AT-125|||U-42126；阿西维辛|||AT-125|||U-42126
Acivicin (AT-125) is a γ-glutamyl transpeptidase (GGT) inhibitor derived from the Streptomyces sviceus natural product. It possesses anti-cancer and anti-parasitic properties and can effectively cross the blood-brain barrier[1][2].
价 格：￥电议型 号：T14114产 地：中国大陆
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T14113Acid-PEG9-NHS ester；化合物 T14113Acid-PEG9-NHS ester
Acid-PEG9-NHS ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T14113产 地：中国大陆
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T14112Acid-PEG6-mono-methyl ester；化合物 T14112Acid-PEG6-mono-methyl ester
Acid-PEG6-mono-methyl ester is a polyethylene glycol (PEG)-based PROTAC linker appropriate for synthesizing PROTACs. [1]
价 格：￥电议型 号：T14112产 地：中国大陆
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T14111Acid-PEG6-C2-Boc；化合物 T14111Acid-PEG6-C2-Boc
Acid-PEG6-C2-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T14111产 地：中国大陆
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T14110Acid-PEG5-TEMPO；化合物 T14110Acid-PEG5-TEMPO
Acid-PEG5-TEMPO is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T14110产 地：中国大陆
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T1411Terbinafine hydrochloride；盐酸特比萘芬KWD 2019|||Terbinafine HCl|||TDT 067 hydrochloride；KWD 2019|||盐酸特比萘芬
Terbinafine hydrochloride (KWD 2019) is a synthetic allylamine derivative structurally related to naftifine. Terbinafine is active against dermatophytes.
价 格：￥电议型 号：T1411产 地：中国大陆
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T14109Acid-PEG5-mono-methyl ester；化合物 T14109Acid-PEG5-mono-methyl ester
Acid-PEG5-mono-methyl ester, a PEG-based PROTAC linker, enables the synthesis of PROTACs[1].
价 格：￥电议型 号：T14109产 地：中国大陆
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T14108Acid-PEG5-C2-Boc；化合物 T14108Acid-PEG5-C2-Boc
Acid-PEG5-C2-Boc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T14108产 地：中国大陆
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T14107Acid-PEG4-S-S-PEG4-acid；化合物 T14107Acid-PEG4-S-S-PEG4-acid
Acid-PEG4-S-S-PEG4-acid is a polyethylene glycol (PEG)-based PROTAC linker, which serves as a key component in the synthesis of PROTACs.
价 格：￥电议型 号：T14107产 地：中国大陆
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T14106Acid-PEG4-mono-methyl ester；化合物 T14106Acid-PEG4-mono-methyl ester
Acid-PEG4-mono-methyl ester, a PEG- and Alkyl/ether-based PROTAC linker, can be employed for PROTAC synthesis[1].
价 格：￥电议型 号：T14106产 地：中国大陆
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T14104Acid-PEG3-SS-PEG3-acid；化合物 T14104Acid-PEG3-SS-PEG3-acid
Acid-PEG3-SS-PEG3-acid is a cleavable 6 unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T14104产 地：中国大陆
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T14103Acid-PEG3-PFP ester；化合物 T14103Acid-PEG3-PFP ester
Acid-PEG3-PFP ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T14103产 地：中国大陆
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T14102Acid-PEG3-mono-methyl ester；化合物 T14102Acid-PEG3-mono-methyl ester
Acid-PEG3-mono-methyl ester, an alkyl/ether-based PROTAC linker, facilitates the synthesis of PROTACs[1].
价 格：￥电议型 号：T14102产 地：中国大陆
