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42

抑制剂 & 化合物

5

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T11940	Malic enzyme inhibitor ME1 ME1	Others	Others
	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。
T18613	MV-1-NH-Me PROTAC IAP binding moiety 2	Others	Others
	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].
T13671	(S,R,S)-AHPC-Me hydrochloride VHL ligand 2 hydrochloride,E3 ligase Ligand 1	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-Me hydrochloride (VHL ligand 2 hydrochloride) is a chemical compound utilized in the synthesis of ARV-771, an exceptionally potent BET protein degrader. This compound selectively degrades BET protein in cells resistant to castration, exhibiting a remarkable DC50 <1 nM. Recognized as VHL ligand 2 hydrochloride, (S,R,S)-AHPC-Me hydrochloride serves as the VHL ligand derived from (S,R,S)-AHPC for the recruitment of von Hippel-Lindau (VHL) protein.
T9016	AI-10-47 1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47	Others	Others
	AI-10-47 (1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47) 是 CBFβ-RUNX 结合的小分子抑制剂(IC50:3.2 μM)。
T18612	Bestatin-amido-Me PROTAC IAP binding moiety 1	Others	Others
	Bestatin-amido-Me, a derivative of Bestatin, acts as an IAP ligand and interacts with ABL inhibitor through a linker to produce SNIPER[1].
T13671L	(S,R,S)-AHPC-Me dihydrochloride VHL ligand 2 dihydrochloride,E3 ligase Ligand 1 dihydrochloride,(S,R,S)-AHPC-Me dihydrochloride (1948273-02-6 free base)	Others	Others
	(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) prote...
T76631	(N-Me-Tyr1,N-Me-Arg7,D-Leu-NHEt8)-Dynorphin A (1-8)
	(N-Me-Tyr1,N-Me-Arg7,D-Leu-NHEt8)-Dynorphin A (1-8) (E-2078) 是一种稳定的 Dynorphin A (1-8) 类似物，是 kappa 阿片受体 (KOR) 激动剂。
T130490	1-(3,4-Dihydroxyphenyl)-1-propanol, 3?,4?-Di-Me et
	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。
T39910	Desmorpholinyl Navitoclax-NH-Me Desmorpholinyl ABT-263-NH-Me,Desmorpholinyl Navitoclax-NH-Me	BCL	Apoptosis
	Desmorpholinyl Navitoclax-NH-Me (Desmorpholinyl ABT-263-NH-Me) is a Bcl-xL inhibitor, which can be employed alongside a CRBN ligand to synthesize XZ739, a PROTAC BCL-XL degrader [1] [2].
T7752	(S,R,S)-AHPC-Me VHL ligand 2,E3 ligase Ligand 1A	Ligand for E3 Ligase	PROTAC
	(S,R,S)-AHPC-Me (E3 ligase Ligand 1A) 是基于 (S,R,S)-AHPC 的的 VHL 配体，可用于募集 von Hippel-Lindau (VHL) 蛋白。它可有效降解去势抵抗性前列腺癌细胞中的 BET 蛋白，DC50<1 nM。它可用于合成 ARV-771。
T18363	Monoethyl pimelate	Others; PROTAC Linker	Others; PROTAC
	Monoethyl pimelate 是一种属于 alkyl/ether 类的 PROTAC linker 可用于特异性的 BCL-XLPROTAC 降解剂 (S,R,S)-AHPC-Me-C7 ester 的合成。
T16236	N-Me-N-bis(PEG2-propargyl)	Others	Others
	N-Me-N-bis(PEG2-propargyl) is a PEG-based linker employed for the synthesis of PROTACs[1].
T18443	N-Me-N-bis(PEG4-C2-Boc)	Others	Others
	N-Me-N-bis(PEG4-C2-Boc) is a PROTAC linker utilizing alkyl and ether functionalities, which is instrumental in PROTAC synthesis. [1]
T18506	NO2-SPP-sulfo-Me	Others	Others
	NO2-SPP-sulfo-Me is a cleavable linker utilized in the synthesis of antibody-drug conjugates (ADC)[1].
T80137	(d(CH2)51,Tyr(Me)2,Dab5,Arg8)-Vasopressin d(CH2)5[Tyr(Me)2, Dab5]AVP	Vasopressin Receptor	GPCR/G Protein
	(d(CH2)51,Tyr(Me)2,Dab5,Arg8)-Vasopressin (d(CH2)5[Tyr(Me)2, Dab5]AVP)作为针对加压素受体V1a的特异性拮抗剂，具有pA2值为6.71。
T18669	(S,R,S)-AHPC-Me-C10-NH2	Others	Others
	(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].
T65182	Fmoc-Cys(Me)-OH
	Fmoc-Cys(Me)-OH 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 T65182，CAS号为 138021-87-1。
T18671	(S,R,S)-AHPC-Me-C7 ester	Others	Others
	(S,R,S)-AHPC-Me-C7 ester is a E3 ligase ligand-linker conjugate used to synthesise BCL-XL PROTAC degraders[1].
T80126	(d(CH2)51,Tyr(Me)2,Orn8)-Oxytocin	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	'(d(CH2)51,Tyr(Me)2,Orn8)-Oxytocin (OVT)' 是催产素受体的一种拮抗剂，主要应用于神经系统疾病的研究领域。
T18847	THP-PEG4-Pyrrolidine(N-Me)-CH2OH	Others	Others
	THP-PEG4-Pyrrolidine(N-Me)-CH2OH, a PEG-based PROTAC linker, facilitates the synthesis of PROTAC K-Ras Degrader-1[1].
T18593	GNF5-amido-Me PROTAC ABL binding moiety 2	Others	Others
	GNF5-amido-Me, the moiety based on GNF5 (ABL inhibitor),binds through a linker to the IAP ligand forming SNIPER[1].
T18670	(S,R,S)-AHPC-Me-C5-COOH	Others	Others
	(S,R,S)-AHPC-Me-C5-COOH is a synthetic E3 ligase ligand-linker conjugate consisting of a VHL ligand and a linker. It finds application in PROTAC DT2216[1].
T18624	NH2-Ph-C4-acid-NH2-Me PROTAC Linker 31	Others	Others
	NH2-Ph-C4-acid-NH2-Me (PROTAC Linker 31) is an alkyl chain-based compound utilized for the synthesis of PROTACs. [1]
T77872	S-Me-DM4
	S-Me-DM4是DM4在胞内酶作用下发生S-甲基化反应形成的代谢产物。DM4本身是一种具有强细胞毒性的含硫醇类微管解聚剂，并可作为ADC Cytotoxin分子应用。
T36360	Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2 Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2
	Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2 is a fluorogenic substrate for matrix metalloproteinase-1 (MMP-1) and MMP-9. Upon cleavage by MMP-1 or MMP-9, N-methylanthranilic acid (Nma) is unquenched and its fluorescence can be used to quantify MMP activity. Nma displays excitation/emission spectra of 340/440 nm, respectively.
T74033	6-Me-ATP
	6-Me-ATP（N6-Methyl-ATP）为ATP的N6修饰衍生物。该化合物与GSK3β结合亲和力显著，能有效作为GSK3β催化底物肽磷酸化的磷酸基团供体。
T19326	Fmoc-Trp(Me)-OH	Others	Others
	Fmoc-Trp(Me)-OH is synthesized by 1-Methyl-Ltrypthophan and N-(9-Fluorenylmethoxycarbonyloxy)succinimide (Fmoc-ONSu) and can be used for peptide or protein synthesis.
T79878	Hydroxy-PP-Me	Apoptosis	Apoptosis
	Hydroxy-PP-Me为一特异性CBR1抑制剂，IC50值为759 nM。该化合物能够抑制血清戒断所诱导的细胞凋亡(apoptosis)。与As2O3单独应用相比，Hydroxy-PP-Me可增强As2O3引发的凋亡细胞死亡效果。
T80073	Dp[Tyr(methyl)2,Arg8]-Vasopressin	Vasopressin Receptor	GPCR/G Protein
	Dp[Tyr(methyl)2,Arg8]-Vasopressin 是一种作用于肽精氨酸加压素 V1b 受体的非选择性拮抗剂。
T80885	Val-Cit-amide-Cbz-N(Me)-Maytansine
	Val-Cit-amide-Cbz-N(Me)-Maytansine是一种可用于构建抗体和双特异性抗原结合分子，能够特异性结合肝细胞生长因子受体c-Met (MET)以及用于制备抗体药物偶联物(antibody-drug conjugates) (ADCs)的化合物。
T76404	[Glp5,(Me)Phe8,Sar9] Substance P (5-11)
	[Glp5,(Me)Phe8,Sar9] Substance P (5-11) (DiMe-C7) 是一种 Substance P 类似物，在大鼠大脑中对神经激肽 1 受体 (NK1R) 的作用与 Substance P 大致相等，但作用时间大大延长。[Glp5,(Me)Phe8,Sar9] Substance P (5-11) 能选择性地激活大鼠大脑间脑和中脑皮层的多巴胺代谢。[Glp5,(Me)Phe8,Sar9] Substance P (5-11) 还可增加大鼠运动活性，诱导成瘾剂寻求行为的恢复。
T76612	(D-Phe5,Cys6,11,N-Me-D-Trp8)-Somatostatin-14 (5-12) amide
	(D-Phe5,Cys6,11,N-Me-D-Trp8)-Somatostatin-14 (5-12) amide (Compound 4) 是一种生长抑素类似物，对 SSTR5、SSTR3、SSTR2、SSTR1和 SSTR4的Kd 分别为 0.61、11.05、23.5、1200 和 >1000 nM。
T75358	DMTr-4'-CF3-5-Me-U-CED phosphoramidite
	DMTr-4'-CF3-5-Me-U-CED phosphoramidite (DMTr-4'-CF3-5-Methyluridine-CED phosphoramidite) 为一种修饰寡脱氧核苷酸 (ODN)，作为用于寡核苷酸标记的染料试剂，在 RNA 研究领域有其应用价值。
T18668	(S,R,S)-AHPC-Me-C10-Br	Others	Others
	(S,R,S)-AHPC-Me-C10-Br is a chemically synthesized conjugate that functions as a ligand-linker for E3 ligases. This compound incorporates a VHL E3 ligase linker and MS432, derived from the MEK1/2 inhibitor PD0325901[1].
T68463	BI-4834
	BI-4834 is a potent and selective Polo-like kinase 1 (PLK1) inhibitor. BI-4834 is also analogue (or Me-Too) of BI-2536. In vitro test shows that BI 4834 inhibits PLK1 with IC50=7.6 nm, but with higher selectivity over the related enzyme PLK3 (IC50 198.4 nm) as BI-2536.
T74034	6-Me-ATP trisodium
	6-Me-ATP trisodium (N6-Methyl-ATP) 是N6-修饰的ATP衍生物，展现对GSK3良好的结合亲和力，可作为GSK3β磷酸化底物肽的磷酸基团供体。
T76590	(d(CH2)51,Tyr(Me)2,Thr4,Orn8,des-Gly-NH29)-Vasotocin
	(d(CH2)51,Tyr(Me)2,Thr4,Orn8,des-Gly-NH29)-Vasotocin，是一种催产素受体拮抗剂，可消除 CA1 锥体神经元中催产素增强的抑制性突触后电流。
T76602	(D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat)
	(D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat) 作为一种CRF拮抗剂，能有效阻断IL-1a诱发的黄体生成素 (LH) 抑制作用。
T36766	Palmitoylcholine (chloride)
	Palmitoylcholine is an acyl choline.1It inhibits protein kinase C activity when used at a concentration of 100 μM.2Palmitoylcholine induces hemolysis in rat erythrocytes.3Plasma levels of palmitoylcholine are decreased in female patients with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).1 1.Germain, A., Barupal, D.K., Levine, S.M., et al.Comprehensive circulatory metabolomics in ME/CFS reveals disrupted metabolism of acyl lipids and steroidsMetabolites10(1)34(2020) 2.Nakadate, T.,...
T75221	2’-O-Me-5-I-U-3’-phosphoramidite
	2’-O-Me-5-I-U-3’-phosphoramidite 为一种嘌呤核苷类似物，以抗肿瘤活性广泛，主要针对惰性淋巴系统恶性肿瘤。其作用机制主要通过抑制 DNA 合成及诱导细胞凋亡(apoptosis)实现。
T80692	β-Glucuronide-NB-bis[N(Me)-methyl ester]-MMAE
	β-Glucuronide-NB-bis[N(Me)-methyl ester]-MMAE 是一种具有选择性的抗增殖活性木耳素-葡糖苷缀合物，对β-葡萄糖醛酸酶处理和未处理的癌细胞体外显示IC50为5.7 nM - 9.7 nM。在HCT-116异种移植小鼠模型中展现出显著的抗肿瘤效果，并且未观察到副作用。
T36404	PRLX-93936
	PRLX-93936 is an analog of erastin that has antitumor activity. It inhibits the hypoxia-inducible factor 1 (HIF-1) signaling pathway under hypoxic conditions (IC50 = 0.09 μM in a cell-based reporter assay). PRLX-93936 (1 μM) also inhibits hypoxia-induced increases in HIF-1α expression in ME-180 cervical cancer cells. It inhibits the growth of HT-1080 fibrosarcoma, OVCAR-5 ovarian cancer, BJELR tumorigenic primary fibroblast, and PANC-1 pancreatic cancer cells with IC50 values of less than 100 nM...

化合物

Malic enzyme inhibitor ME1

Cat.No: T11940

Synonym: ME1

Target: Others

Cat.No: T18613

Synonym: PROTAC IAP binding moiety 2

Target: Others

(S,R,S)-AHPC-Me hydrochloride

Cat.No: T13671

Synonym: VHL ligand 2 hydrochloride,E3 ligase Ligand 1

Target: Others, Ligand for E3 Ligase

Cat.No: T9016

Synonym: 1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47

Target: Others

Bestatin-amido-Me

Cat.No: T18612

Synonym: PROTAC IAP binding moiety 1

Target: Others

(S,R,S)-AHPC-Me dihydrochloride

Cat.No: T13671L

Synonym: VHL ligand 2 dihydrochloride,E3 ligase Ligand 1 dihydrochloride,(S,R,S)-AHPC-Me dihydrochloride (1948273-02-6 free base)

Target: Others

(N-Me-Tyr1,N-Me-Arg7,D-Leu-NHEt8)-Dynorphin A (1-8)

Cat.No: T76631

1-(3,4-Dihydroxyphenyl)-1-propanol, 3?,4?-Di-Me et

Cat.No: T130490

Desmorpholinyl Navitoclax-NH-Me

Cat.No: T39910

Synonym: Desmorpholinyl ABT-263-NH-Me,Desmorpholinyl Navitoclax-NH-Me

Target: BCL

(S,R,S)-AHPC-Me

Cat.No: T7752

Synonym: VHL ligand 2,E3 ligase Ligand 1A

Target: Ligand for E3 Ligase

Monoethyl pimelate

Cat.No: T18363

Target: Others, PROTAC Linker

N-Me-N-bis(PEG2-propargyl)

Cat.No: T16236

Target: Others

N-Me-N-bis(PEG4-C2-Boc)

Cat.No: T18443

Target: Others

NO2-SPP-sulfo-Me

Cat.No: T18506

Target: Others

(d(CH2)51,Tyr(Me)2,Dab5,Arg8)-Vasopressin

Cat.No: T80137

Synonym: d(CH2)5[Tyr(Me)2, Dab5]AVP

Target: Vasopressin Receptor

(S,R,S)-AHPC-Me-C10-NH2

Cat.No: T18669

Target: Others

Fmoc-Cys(Me)-OH

Cat.No: T65182

(S,R,S)-AHPC-Me-C7 ester

Cat.No: T18671

Target: Others

(d(CH2)51,Tyr(Me)2,Orn8)-Oxytocin

Cat.No: T80126

Target: Oxytocin Receptor

THP-PEG4-Pyrrolidine(N-Me)-CH2OH

Cat.No: T18847

Target: Others

Cat.No: T18593

Synonym: PROTAC ABL binding moiety 2

Target: Others

(S,R,S)-AHPC-Me-C5-COOH

Cat.No: T18670

Target: Others

NH2-Ph-C4-acid-NH2-Me

Cat.No: T18624

Synonym: PROTAC Linker 31

Target: Others

Cat.No: T77872

Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2

Cat.No: T36360

Synonym: Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2

Cat.No: T74033

Fmoc-Trp(Me)-OH

Cat.No: T19326

Target: Others

Cat.No: T79878

Target: Apoptosis

Dp[Tyr(methyl)2,Arg8]-Vasopressin

Cat.No: T80073

Target: Vasopressin Receptor

Val-Cit-amide-Cbz-N(Me)-Maytansine

Cat.No: T80885

[Glp5,(Me)Phe8,Sar9] Substance P (5-11)

Cat.No: T76404

(D-Phe5,Cys6,11,N-Me-D-Trp8)-Somatostatin-14 (5-12) amide

Cat.No: T76612

DMTr-4'-CF3-5-Me-U-CED phosphoramidite

Cat.No: T75358

(S,R,S)-AHPC-Me-C10-Br

Cat.No: T18668

Target: Others

Cat.No: T68463

6-Me-ATP trisodium

Cat.No: T74034

(d(CH2)51,Tyr(Me)2,Thr4,Orn8,des-Gly-NH29)-Vasotocin

Cat.No: T76590

(D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat)

Cat.No: T76602

Palmitoylcholine (chloride)

Cat.No: T36766

2’-O-Me-5-I-U-3’-phosphoramidite

Cat.No: T75221

β-Glucuronide-NB-bis[N(Me)-methyl ester]-MMAE

Cat.No: T80692

Cat.No: T36404

Cat. No.	Product Name	Target	Signaling Pathways
T3S2259	Methyl eugenol 4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	Methyl eugenol (4-allylveratrole) 是一种苯丙类化合物，存在于植物叶子、果实、根茎中，当植物相应的部位因食草动物进食而受损时，就会释放。它可用于消灭雄性东方果蝇。
T82337	Ganoderic acid Me
	Ganoderic acid Me是来源于ganoderma lucidum的三萜类化合物。
T81905	Lucidin-ω-Me ether
	Lucidin-ω-Me ether（化合物2），一种自Knoxia valerianoides的根中分离得到的化合物，具有抑制体外晚期糖基化终末产物（AGE）形成的活性，其IC50为62.79 μM。
T4S0969	Obtusifolin 决明蒽醌,决明蒽醌；美决明子素	Antioxidant; NF-κB	NF-κB; oxidation-reduction
	Obtusifolin 是分离自决明子的种子中，能够抑制NF-kB 通路，调节气道上皮细胞中 MUC5AC 粘蛋白的基因表达和产生。它通过靶向甲状旁腺激素相关蛋白来抑制邻苯二甲酸酯诱导的乳腺癌骨转移。
T80941	Triptonoterpene Me ether
	Triptonoterpene Me ether（compound 5）为一种从中药雷公藤（Tripterygium wilfordii Hook. f.）分离出的松香烷型二萜类化合物。

天然产物

Cat.No: T3S2259

Synonym: 4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚

Target: GABA Receptor

Ganoderic acid Me

Cat.No: T82337

Lucidin-ω-Me ether

Cat.No: T81905

Cat.No: T4S0969

Synonym: 决明蒽醌,决明蒽醌；美决明子素

Target: Antioxidant, NF-κB

Triptonoterpene Me ether

Cat.No: T80941

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