me

DCPLA-ME (2-[(2-Pentylcyclopropyl)methyl]cyclopropaneoctanoic acid methyl ester) 是 DCPLA 的甲酯形式。DCPLA-ME 是一种有效的 PKCε 激活剂。DCPLA-ME 可用于研究神经退行性疾病。

Malic enzyme inhibitor ME1 (ME1) 是苹果酸酶的特异性抑制剂 (IC50 = 0.15 μM)。 苹果酸酶抑制剂 ME1 降低细胞活力 代谢活性。

ME-3221是一种血管紧张素AT1受体拮抗剂，可预防老年中风易发性高血压大鼠的高血压并发症。

20-HC-Me-Pyrrolidine FA 是一种有效的 Aster 蛋白抑制剂，对 Aster-A、Aster-B 和 Aster-C 具有抑制作用，抑制 Aster 蛋白结合和转移胆固醇。20-HC-Me-Pyrrolidine FA 可用于研究脂类代谢。

(S,R,S)-AHPC-Me hydrochloride (VHL ligand 2 hydrochloride) 是一种化学化合物，应用于合成ARV-771，一种极其强效的BET蛋白降解剂。该化合物在对去势抵抗的细胞中特异性地降解BET蛋白，其DC50值显著小于1 nM。作为VHL ligand 2 hydrochloride，(S,R,S)-AHPC-Me hydrochloride作为来源于(S,R,S)-AHPC的VHL配体，用于募集von Hippel-Lindau (VHL)蛋白。

ME1111 是毛癣菌琥珀酸脱氢酶的抑制剂，也是一种抗真菌剂，对皮癣菌具有活性。ME1111 能很好地穿透人体指甲，可用于甲癣研究。

Fmoc-Gly-Ser(psi(Me,Me)pro)-OH acetate 是一种二肽。

Fmoc-Gly-Thr(psi(Me,Me)pro)-OH 是一个二肽。

Desmorpholinyl Navitoclax-NH-Me (Desmorpholinyl ABT-263-NH-Me) 是一种 Bcl-xL 抑制剂，这是一种 PROTAC BCL-XL 降解剂,可与 CRBN 配体一起使用以合成 XZ739 [1] [2]。

N-Me-aminopyrimidinone9 是一种钠通道拮抗剂。

N-Me-L-Ala-maytansinol used for making antibody-drug conjugate (ADC),is a hydrophobic, cell permeable payload.

1-(3,4-Dihydroxyphenyl)-1-propanol, 3?,4?-Di-Me et 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T130490。

(S,R,S)-AHPC-Me dihydrochloride, also known as VHL ligand 2 dihydrochloride, is a chemical compound utilized in the synthesis of ARV-771. ARV-771, a BET PROTAC degrader relying on von Hippel-Landau (VHL) E3 ligase, demonstrates potent degradation of BET protein in castration-resistant prostate cancer (CRPC) cells, with a DC50 of less than 1 nM. This compound serves as the VHL ligand, specifically the (S,R,S)-AHPC-based VHL ligand, that facilitates the recruitment of von Hippel-Lindau (VHL) protein.

N-Me-N-bis(PEG2-propargyl) is a PEG-based linker employed for the synthesis of PROTACs[1].

N-Me-N-bis-PEG4 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.

N-Me-N-bis-PEG3 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.

N-Me-N-bis(PEG4-acid) 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.

N-Me-N-bis(PEG4-C2-Boc) is a PROTAC linker utilizing alkyl and ether functionalities, which is instrumental in PROTAC synthesis. [1]

NO2-SPP-sulfo-Me is a cleavable linker utilized in the synthesis of antibody-drug conjugates (ADC)[1].

GNF5-amido-Me, the moiety based on GNF5 (ABL inhibitor),binds through a linker to the IAP ligand forming SNIPER[1].

MV-1-NH-Me, an MV-1-derived IAP ligand, connects to an ABL inhibitor through a linker, resulting in the formation of SNIPER[1].

NH2-Ph-C4-acid-NH2-Me (PROTAC Linker 31) is an alkyl chain-based compound utilized for the synthesis of PROTACs. [1]

(S,R,S)-AHPC-Me-C10-Br是一种化学合成的共轭物和E3连接酶的配体连接器(ligand-linker)，由MEK1 2抑制剂的的MS432和VHL E3 连接酶连接器组成。

(S,R,S)-AHPC-Me-C10-NH2 is a chemical compound consisting of a synthesized E3 ligase ligand-linker conjugate that incorporates both a VHL ligand and a linker. This compound, (S,R,S)-AHPC-Me-C10-NH2, finds application in PROTAC MS432[1].