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Search Results for " ligand "

1218

抑制剂 & 化合物

47

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T17870	cIAP1 ligand 1 E3 ligase Ligand 12	Others	Others
	cIAP1 ligand 1 (E3 ligase Ligand 12) 是基于 LCL161 衍生物的细胞凋亡蛋白配体，可募集 IAP 泛素连接酶以降解靶蛋白，可用于和雄激素受体配体偶联开发蛋白降解剂，可用于研究前列腺癌。
TP1484L	α2β1 Integrin Ligand Peptide acetate α2β1 Integrin Ligand Peptide acetate (134580-64-6)	Integrin	Cytoskeletal Signaling
	α2β1 Integrin Ligand Peptide acetate (α2β1 Integrin Ligand Peptide acetate (134580-64-6)) 是 α2β1 整合素受体的潜在拮抗剂。它与细胞膜上的 α2β1 整合素受体相互作用，介导细胞外信号进入细胞。
T13510	Sigma-LIGAND-1	Sigma receptor	GPCR/G Protein
	Sigma-LIGAND-1 是一种选择性 sigma 受体配体，在 DTG 和 PPP 位点的 IC50 分别为 16 nM，19 nM。Sigma-LIGAND-1 对多巴胺 D2 受体的 Ki 为 4000 nM。
T10053	5HT6-ligand-1	5-HT Receptor	GPCR/G Protein; Neuroscience
	5HT6-ligand-1 是一种具有口服活性的 5-HT6 受体配体 (Ki = 1.43 nM)。
T5835	PROTAC ERRα ligand 2	Estrogen Receptor/ERR; Estrogen/progestogen Receptor	Endocrinology/Hormones
	PROTAC ERRα ligand 2 是雌激素相关受体 α （ERRα）反向激动剂。它对 ERRα (IC50=5.67 nM) 的抑制作用比 XCT790 (IC50=61.3 nM) 高效约 11 倍。
T15191	PROTAC ERRα ligand 1	Estrogen Receptor/ERR; Estrogen/progestogen Receptor	Endocrinology/Hormones
	PROTAC ERRα ligand 1 是一种雌激素相关受体 α (ERRα) 拮抗剂，能够作用于 ERRα (IC50:0.04 μM)和 ERRγ (IC50:2.8 μM)。
TP1496L	p5 Ligand for Dnak and DnaJ acetate p5 Ligand for Dnak and DnaJ acetate(209518-24-1 free base)	HSP	Cytoskeletal Signaling; Metabolism
	p5 Ligand for Dnak and DnaJ acetate(209518-24-1 free base) 是一种九肽。它是 DnaK（大肠杆菌 Hsp70）和 DnaJ（大肠杆菌 Hsp40）的高亲和力配体。
T38476	Metallo β-lactamase ligand 1	Antibacterial	Microbiology/Virology
	Metallo β-lactamase ligand 1 是B 类β-内酰胺酶的抑制剂，具有抗菌活性。
T12551	PROTAC BRD4 ligand-1	Epigenetic Reader Domain; Ligands for Target Protein for PROTAC	Chromatin/Epigenetic; PROTAC
	PROTAC BRD4 ligand-1 是 PROTAC GNE-987 靶向 BRD4 蛋白的配体，也是一种 BET 的抑制剂。
T60015	TSPO ligand-2 Carbonic acid	AUTACs	PROTAC
	TSPO ligand-2 (Carbonic acid) 是 AUTAC1 的配体，AUTAC1含有一个对氟苄基鸟嘌呤和一个烟曲霉醇部分。
T17879	E3 ligase Ligand 8	Others; Ligand for E3 Ligase	Others; PROTAC
	E3 ligase Ligand 8 是 E3 泛素连接酶配体。它能够利用 linker 与靶蛋白配体连接，形成 PROTAC 分子。PROTAC 可诱导促癌蛋白发生泛素化降解。
TP1704	Galanin Receptor Ligand M35 TFA	Neuropeptide Y Receptor	GPCR/G Protein; Neuroscience
	Galanin Receptor Ligand M35 TFA(142846-71-7 free base) 是一种高亲和力配体和甘丙肽受体拮抗剂 (Kd=0.1 nM)。
T9809	E3 ligase Ligand 23	Ligand for E3 Ligase	PROTAC
	E3 ligase Ligand 23 是一种 cereblon 结合剂，可通过泛素蛋白酶体降解 Ikaros 或 Aiolos。
T9360	CRBN ligand-9 2-(2,6-dioxopiperidin-3-yl)-5-nitroisoindoline-1,3-dione	Ligand for E3 Ligase	PROTAC
	CRBN ligand-9 (2-(2,6-dioxopiperidin-3-yl)-5-nitroisoindoline-1,3-dione) 表现出对 CRBN 的抑制作用。
T13848	SMARCA-BD ligand 1 for Protac	Epigenetic Reader Domain	Chromatin/Epigenetic
	SMARCA-BD ligand 1 for Protac 能够与 BAF ATPase 亚基 SMARCA2 结合，可用于 PROTAC 技术，用于降解 SMARCA2。
T13890	SMARCA-BD ligand 1 for Protac dihydrochloride	Epigenetic Reader Domain	Chromatin/Epigenetic
	SMARCA-BD ligand 1 for Protac dihydrochloride 是一种能够与 BAF ATPase 亚基 SMARCA2 结合的化合物，基于 PROTAC 技术，使 SMARCA2 降解。
T7763	Thalidomide-4-OH Cereblon ligand 2,E3 ligase Ligand 2	Ligand for E3 Ligase	PROTAC
	Thalidomide-4-OH (E3 ligase Ligand 2) 是一种基于 Thalidomide 的 Cereblon 配体，可用于募集 CRBN 蛋白。它能够利用 linker 与靶蛋白配体连接，得到 PROTAC 分子。
T39997	PROTAC CDK9 ligand-1 PROTAC CDK9 ligand-1
	PROTAC CDK9 ligand-1 is a CDK9 ligand that can be used in the synthesis of PROTACs.
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。
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.
T39628	PROTAC BRD4 ligand-2 PROTAC BRD4 ligand-2
	PROTAC BRD4 ligand-2 is a ligand for target BRD4 protein for PROTAC CFT-2718.
T7753	Thalidomide-O-COOH Cereblon ligand 3,E3 ligase Ligand 3,TCE35031	Others; Ligand for E3 Ligase	Others; PROTAC
	Thalidomide-O-COOH (Cereblon ligand 3) 是一种基于 Thalidomide 的 Cereblon 配体，可用于募集 CRBN 蛋白。它能够利用 linker 与靶蛋白配体连接，得到 PROTAC 分子。
T17869	cIAP1 ligand 2 E3 ligase Ligand 11	Others	Others
	cIAP1 ligand 2, a derivative of LCL161, is an IAP ligand that can be connected to the ABL ligand for protein via a linker, resulting in the formation of SNIPER.
T39629	BRD4 ligand-Linker Conjugate 1 BRD4 ligand-Linker Conjugate 1
	BRD4 Ligand-Linker Conjugate 1 is a compound consisting of a ligand and a linker, specifically designed to bind to the target protein BRD4. This conjugate serves as a valuable tool for synthesizing PROTACs, molecules utilized for targeted protein degradation.
T17877	VH032-cyclopropane-F VHL ligand 3,E3 ligase Ligand 19,Phenolic VH101	Others; Ligand for E3 Ligase	Others; PROTAC
	VH032-cyclopropane-F (Phenolic VH101) 是基于 VH032 的 VHL 配体。它能够利用 linker 与靶蛋白配体连接，得到 PROTAC 分子，如 PROTAC 1。PROTAC 1 是 SMARCA2 和 SMARCA4 的部分降解剂。
T17916	Pomalidomide-PEG4-C2-NH2 Cereblon Ligand-Linker Conjugates 8,E3 Ligase Ligand-Linker Conjugates 22	Others; Ligand for E3 Ligase	Others; PROTAC
	Pomalidomide-PEG4-C2-NH2 (E3 Ligase Ligand-Linker Conjugates 22) 是一种合成的 E3 连接酶配体- linker 偶联物，用于 PROTAC 技术中。
T73599	TSPO ligand-1	Autophagy	Autophagy
	TSPO ligand-1 对外周和中枢苯二氮卓受体有亲和力。TSPO ligand-1 是一种线粒体外膜跨膜结构域上与 AUTAC4 结合的蛋白，可诱导线粒体自噬 (autophagy) 促进胞内线粒体更新。TSPO ligand-1 参与胆固醇在胞内的转运，可作为脑损伤和神经变性的生物标志物。
T39609	cIAP1 Ligand-Linker Conjugates 16 cIAP1 Ligand-Linker Conjugates 16
	cIAP1 Ligand-Linker Conjugates 16 refers to a specific type of ligase ligand-linker conjugate, possessing the ability to engage with E3 ligases, which finds application in the synthesis of PROTACs.
T17325	Pomalidomide-PEG4-C-COOH Cereblon Ligand -Linker Conjugates 1,E3 Ligase Ligand-Linker Conjugates 1	Others; E3 Ligase Ligand-Linker Conjugate	Others; PROTAC
	Pomalidomide-PEG4-C-COOH (E3 Ligase Ligand-Linker Conjugates 1) 包含基于 Pomalidomide 的 cereblon 配体和 4 个单元 PEG linker，是一种合成的 E3 连接酶配体-linker 偶联物。
T15189	Thalidomide-O-amido-C4-N3 E3 ligase Ligand-Linker Conjugates 18,Cereblon Ligand-Linker Conjugates 4	Others; Ligand for E3 Ligase	Others; PROTAC
	Thalidomide-O-amido-C4-N3 (Cereblon Ligand-Linker Conjugates 4) 是一种 E3 连接酶配体- linker 偶联物，包含基于 Thalidomide 的 cereblon 配体和 linker。
T17919	Thalidomide-O-amido-C6-NH2 TFA E3 Ligase Ligand-Linker Conjugates 25 Trifluoroacetate,Cereblon Ligand-Linker Conjugates 11 TFA,E3 Ligase Ligand-Linker Conjugates 25 TFA	Others; Ligand for E3 Ligase	Others; PROTAC
	Thalidomide-O-amido-C6-NH2 TFA (Cereblon Ligand-Linker Conjugates 11 TFA) 包含基于 Thalidomide 的 cereblon 配体和 1 个 linker，是一种合成的 E3 连接酶配体-linker 偶联物。可用于 PROTAC 的合成分子。
T40142	Thalidomide-NH-CBP/p300 ligand 2 Thalidomide-NH-CBP/p300 ligand 2
	Thalidomide-NH-CBP/p300 ligand 2 (P-007) is a PROTAC-based compound designed to degrade CBP and p300, acting as a functional antagonist (WO2020173440).
T7760	Thalidomide-O-amido-C3-NH2 TFA Cereblon Ligand-Linker Conjugates 16 TFA,E3 Ligase Ligand-Linker Conjugates 52 TFA	E3 Ligase Ligand-Linker Conjugate; Ligand for E3 Ligase	PROTAC
	Thalidomide-O-amido-C3-NH2 TFA (Cereblon Ligand-Linker Conjugates 16 TFA) 包含基于 Thalidomide 的 cereblon 配体和 1 个 linker，是一种合成的 E3 连接酶配体-linker 偶联物，。
T7759	Thalidomide-O-amido-C4-NH2 TFA E3 ligase Ligand-Linker Conjugates 19 TFA,Cereblon Ligand-Linker Conjugates 6 TFA	E3 Ligase Ligand-Linker Conjugate	PROTAC
	Thalidomide-O-amido-C4-NH2 TFA (E3 ligase Ligand-Linker Conjugates 19 TFA) 包含基于 Thalidomide 的 cereblon 配体和 1 个 linker，是一种合成的 E3 连接酶配体-linker 偶联物。
T7758	Thalidomide-O-amido-PEG3-C2-NH2 TFA E3 ligase Ligand-Linker Conjugates 14 TFA,Cereblon Ligand-Linker Conjugates 3 (TFA)	Others; E3 Ligase Ligand-Linker Conjugate; Ligand for E3 Ligase	Others; PROTAC
	Thalidomide-O-amido-PEG3-C2-NH2 TFA (Cereblon Ligand-Linker Conjugates 3 (TFA)) 包含基于 Thalidomide 的 cereblon 配体和 3 个单元的 PEG linker，是一种合成的 E3 连接酶配体-linker 偶联物。
T17918	Thalidomide-O-amido-PEG2-C2-NH2 TFA E3 Ligase Ligand-Linker Conjugates 24 TFA,Cereblon Ligand-Linker Conjugates 10 TFA	Others; E3 Ligase Ligand-Linker Conjugate	Others; PROTAC
	Thalidomide-O-amido-PEG2-C2-NH2 TFA (E3 Ligase Ligand-Linker Conjugates 24 TFA) 包含基于 Thalidomide 的 cereblon 配体和 2 个单元的 PEG linker，是一种合成的 E3 连接酶配体-linker 偶联物。
T17922	(S,R,S)-AHPC-PEG3-NH2 hydrochloride VHL Ligand-Linker Conjugates 1 hydrochloride,E3 ligase Ligand-Linker Conjugates 5,VH032-PEG3-NH2 hydrochloride,VHL Ligand-Linker Conjugates 1 HCl	Others; E3 Ligase Ligand-Linker Conjugate	Others; PROTAC
	(S,R,S)-AHPC-PEG3-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 5) 是一种 E3 ligase ligand-linker conjugate，包含了 (S,R,S)-AHPC-based VHL ligand 和 3-unit PEG linker。
T82174	hRIO2 kinase ligand-1	Others	Others
	hRIO2 kinase ligand-1 是一种有效的 hRIO2 激酶的配体（Kd：520 nM）。
T17921	(S,R,S)-AHPC-PEG4-N3 VH032-PEG4-N3,VHL Ligand-Linker Conjugates 5,E3 ligase Ligand-Linker Conjugates 4	Others; PROTAC Linker	Others; PROTAC
	(S,R,S)-AHPC-PEG4-N3 (VHL Ligand-Linker Conjugates 5) is a synthesized conjugate that functions as a ligand-linker in E3 ligase-based systems. It is composed of the (S,R,S)-AHPC VHL ligand and a 4-unit PEG linker, both commonly employed in PROTAC technology.
T39440	CXCL12 ligand 1
	CXCL12 ligand 1 is the first ligand of the sY12-binding pocket on chemokine CXCL12 .
T17920	(S,R,S)-AHPC-PEG1-N3 VHL Ligand-Linker Conjugates 9,VH032-PEG1-N3,E3 ligase Ligand-Linker Conjugates 3	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-PEG1-N3 (E3 ligase Ligand-Linker Conjugates 3) 是 E3 连接酶配体和linker 连接得到的偶联物，包含基于 (S,R,S)-AHPC 的 VHL 配体和 1 个单元 PEG linker。
T17909	(S,R,S)-AHPC-PEG3-N3 VHL Ligand-Linker Conjugates 8,VH032-PEG3-N3,E3 ligase Ligand-Linker Conjugates 12	Others; E3 Ligase Ligand-Linker Conjugate; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-PEG3-N3 (VHL Ligand-Linker Conjugates 8) 包含基于 (S,R,S)-AHPC 的 VHL 配体和 3 个单元 PEG linker，是一种合成的 E3 连接酶配体-linker 偶联物。
T17889	cIAP1 Ligand-Linker Conjugates 14 E3 ligase Ligand-Linker Conjugates 36	Others	Others
	cIAP1 Ligand-Linker Conjugates 14 consist of an IAP ligand that targets the E3 ubiquitin ligase and a PROTAC linker. These conjugates, known as cIAP1 Ligand-Linker Conjugates 14, are used in the development of SNIPERs[1].
T17896	cIAP1 Ligand-Linker Conjugates 4 E3 ligase Ligand-Linker Conjugates 42	Others	Others
	cIAP1 Ligand-Linker Conjugates 4 is a chemical compound that comprises an IAP ligand specifically designed for the E3 ubiquitin ligase and a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 4, has the potential to be utilized in the development of SNIPERs[1].
T17885	cIAP1 Ligand-Linker Conjugates 11 E3 ligase Ligand-Linker Conjugates 33	Others	Others
	cIAP1 Ligand-Linker Conjugates 11 is a chemical compound that combines an IAP ligand specifically designed for the E3 ubiquitin ligase with a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 11, is useful in the development of SNIPERs[1], allowing for the targeted degradation of proteins.
T17891	cIAP1 Ligand-Linker Conjugates 2 E3 ligase Ligand-Linker Conjugates 37	Others	Others
	cIAP1 Ligand-Linker Conjugates 2 is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase with a PROTAC linker. This compound is particularly useful in the design of SNIPERs [1].
T17893	cIAP1 Ligand-Linker Conjugates 5 E3 ligase Ligand-Linker Conjugates 39	Others	Others
	cIAP1 Ligand-Linker Conjugates 5 is a chemical compound consisting of an IAP ligand that targets the E3 ubiquitin ligase, and a PROTAC linker. This compound, cIAP1 Ligand-Linker Conjugates 5, is specifically designed for the development of SNIPERs[1].
T18640	(S,R,S)-AHPC-C4-NH2 hydrochloride VH032-C4-NH2 hydrochloride,E3 ligase Ligand-Linker Conjugates 28,VHL Ligand-Linker Conjugates 13	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-C4-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 28) 是一种合成的 E3 连接酶配体- linker 偶联物，包含基于 (S,R,S)-AHPC 的 VHL 配体和 linker。
T17908	VHL Ligand-Linker Conjugates 15 E3 Ligase Ligand-Linker Conjugates 56	Others	Others
	VHL Ligand-Linker Conjugates 15 is a chemical compound that combines a VHL ligand, which targets the E3 ubiquitin ligase, with a PROTAC linker. It is specifically designed for the creation of PROTACs[1].
T15190L	(S,R,S)-AHPC-PEG4-NH2 VHL Ligand-Linker Conjugates 4,E3 ligase Ligand-Linker Conjugates 7 Free Base,VH032-PEG4-NH2	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-PEG4-NH2 (VHL Ligand-Linker Conjugates 4) 是一种合成的 E3 连接酶配体-接头偶联物，包含基于 (S,R,S)-AHPC 的 VHL 配体和 4 单元 PEG 接头。

化合物

cIAP1 ligand 1

Cat.No: T17870

Synonym: E3 ligase Ligand 12

Target: Others

α2β1 Integrin Ligand Peptide acetate

Cat.No: TP1484L

Synonym: α2β1 Integrin Ligand Peptide acetate (134580-64-6)

Target: Integrin

Sigma-LIGAND-1

Cat.No: T13510

Target: Sigma receptor

5HT6-ligand-1

Cat.No: T10053

Target: 5-HT Receptor

PROTAC ERRα ligand 2

Cat.No: T5835

Target: Estrogen Receptor/ERR, Estrogen/progestogen Receptor

PROTAC ERRα ligand 1

Cat.No: T15191

Target: Estrogen Receptor/ERR, Estrogen/progestogen Receptor

p5 Ligand for Dnak and DnaJ acetate

Cat.No: TP1496L

Synonym: p5 Ligand for Dnak and DnaJ acetate(209518-24-1 free base)

Target: HSP

Metallo β-lactamase ligand 1

Cat.No: T38476

Target: Antibacterial

PROTAC BRD4 ligand-1

Cat.No: T12551

Target: Epigenetic Reader Domain, Ligands for Target Protein for PROTAC

TSPO ligand-2

Cat.No: T60015

Synonym: Carbonic acid

Target: AUTACs

E3 ligase Ligand 8

Cat.No: T17879

Target: Others, Ligand for E3 Ligase

Galanin Receptor Ligand M35 TFA

Cat.No: TP1704

Target: Neuropeptide Y Receptor

E3 ligase Ligand 23

Cat.No: T9809

Target: Ligand for E3 Ligase

CRBN ligand-9

Cat.No: T9360

Synonym: 2-(2,6-dioxopiperidin-3-yl)-5-nitroisoindoline-1,3-dione

Target: Ligand for E3 Ligase

SMARCA-BD ligand 1 for Protac

Cat.No: T13848

Target: Epigenetic Reader Domain

SMARCA-BD ligand 1 for Protac dihydrochloride

Cat.No: T13890

Target: Epigenetic Reader Domain

Thalidomide-4-OH

Cat.No: T7763

Synonym: Cereblon ligand 2,E3 ligase Ligand 2

Target: Ligand for E3 Ligase

PROTAC CDK9 ligand-1

Cat.No: T39997

Synonym: PROTAC CDK9 ligand-1

(S,R,S)-AHPC-Me

Cat.No: T7752

Synonym: VHL ligand 2,E3 ligase Ligand 1A

Target: Ligand for E3 Ligase

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

Cat.No: T13671

Synonym: VHL ligand 2 hydrochloride,E3 ligase Ligand 1

Target: Others, Ligand for E3 Ligase

PROTAC BRD4 ligand-2

Cat.No: T39628

Synonym: PROTAC BRD4 ligand-2

Thalidomide-O-COOH

Cat.No: T7753

Synonym: Cereblon ligand 3,E3 ligase Ligand 3,TCE35031

Target: Others, Ligand for E3 Ligase

cIAP1 ligand 2

Cat.No: T17869

Synonym: E3 ligase Ligand 11

Target: Others

BRD4 ligand-Linker Conjugate 1

Cat.No: T39629

Synonym: BRD4 ligand-Linker Conjugate 1

VH032-cyclopropane-F

Cat.No: T17877

Synonym: VHL ligand 3,E3 ligase Ligand 19,Phenolic VH101

Target: Others, Ligand for E3 Ligase

Pomalidomide-PEG4-C2-NH2

Cat.No: T17916

Synonym: Cereblon Ligand-Linker Conjugates 8,E3 Ligase Ligand-Linker Conjugates 22

Target: Others, Ligand for E3 Ligase

TSPO ligand-1

Cat.No: T73599

Target: Autophagy

cIAP1 Ligand-Linker Conjugates 16

Cat.No: T39609

Synonym: cIAP1 Ligand-Linker Conjugates 16

Pomalidomide-PEG4-C-COOH

Cat.No: T17325

Synonym: Cereblon Ligand -Linker Conjugates 1,E3 Ligase Ligand-Linker Conjugates 1

Target: Others, E3 Ligase Ligand-Linker Conjugate

Thalidomide-O-amido-C4-N3

Cat.No: T15189

Synonym: E3 ligase Ligand-Linker Conjugates 18,Cereblon Ligand-Linker Conjugates 4

Target: Others, Ligand for E3 Ligase

Thalidomide-O-amido-C6-NH2 TFA

Cat.No: T17919

Synonym: E3 Ligase Ligand-Linker Conjugates 25 Trifluoroacetate,Cereblon Ligand-Linker Conjugates 11 TFA,E3 Ligase Ligand-Linker Conjugates 25 TFA

Target: Others, Ligand for E3 Ligase

Thalidomide-NH-CBP/p300 ligand 2

Cat.No: T40142

Synonym: Thalidomide-NH-CBP/p300 ligand 2

Thalidomide-O-amido-C3-NH2 TFA

Cat.No: T7760

Synonym: Cereblon Ligand-Linker Conjugates 16 TFA,E3 Ligase Ligand-Linker Conjugates 52 TFA

Target: E3 Ligase Ligand-Linker Conjugate, Ligand for E3 Ligase

Thalidomide-O-amido-C4-NH2 TFA

Cat.No: T7759

Synonym: E3 ligase Ligand-Linker Conjugates 19 TFA,Cereblon Ligand-Linker Conjugates 6 TFA

Target: E3 Ligase Ligand-Linker Conjugate

Thalidomide-O-amido-PEG3-C2-NH2 TFA

Cat.No: T7758

Synonym: E3 ligase Ligand-Linker Conjugates 14 TFA,Cereblon Ligand-Linker Conjugates 3 (TFA)

Target: Others, E3 Ligase Ligand-Linker Conjugate, Ligand for E3 Ligase

Thalidomide-O-amido-PEG2-C2-NH2 TFA

Cat.No: T17918

Synonym: E3 Ligase Ligand-Linker Conjugates 24 TFA,Cereblon Ligand-Linker Conjugates 10 TFA

Target: Others, E3 Ligase Ligand-Linker Conjugate

(S,R,S)-AHPC-PEG3-NH2 hydrochloride

Cat.No: T17922

Synonym: VHL Ligand-Linker Conjugates 1 hydrochloride,E3 ligase Ligand-Linker Conjugates 5,VH032-PEG3-NH2 hydrochloride,VHL Ligand-Linker Conjugates 1 HCl

Target: Others, E3 Ligase Ligand-Linker Conjugate

hRIO2 kinase ligand-1

Cat.No: T82174

Target: Others

(S,R,S)-AHPC-PEG4-N3

Cat.No: T17921

Synonym: VH032-PEG4-N3,VHL Ligand-Linker Conjugates 5,E3 ligase Ligand-Linker Conjugates 4

Target: Others, PROTAC Linker

CXCL12 ligand 1

Cat.No: T39440

(S,R,S)-AHPC-PEG1-N3

Cat.No: T17920

Synonym: VHL Ligand-Linker Conjugates 9,VH032-PEG1-N3,E3 ligase Ligand-Linker Conjugates 3

Target: Others, Ligand for E3 Ligase

(S,R,S)-AHPC-PEG3-N3

Cat.No: T17909

Synonym: VHL Ligand-Linker Conjugates 8,VH032-PEG3-N3,E3 ligase Ligand-Linker Conjugates 12

Target: Others, E3 Ligase Ligand-Linker Conjugate, Ligand for E3 Ligase

cIAP1 Ligand-Linker Conjugates 14

Cat.No: T17889

Synonym: E3 ligase Ligand-Linker Conjugates 36

Target: Others

cIAP1 Ligand-Linker Conjugates 4

Cat.No: T17896

Synonym: E3 ligase Ligand-Linker Conjugates 42

Target: Others

cIAP1 Ligand-Linker Conjugates 11

Cat.No: T17885

Synonym: E3 ligase Ligand-Linker Conjugates 33

Target: Others

cIAP1 Ligand-Linker Conjugates 2

Cat.No: T17891

Synonym: E3 ligase Ligand-Linker Conjugates 37

Target: Others

cIAP1 Ligand-Linker Conjugates 5

Cat.No: T17893

Synonym: E3 ligase Ligand-Linker Conjugates 39

Target: Others

(S,R,S)-AHPC-C4-NH2 hydrochloride

Cat.No: T18640

Synonym: VH032-C4-NH2 hydrochloride,E3 ligase Ligand-Linker Conjugates 28,VHL Ligand-Linker Conjugates 13

Target: Others, Ligand for E3 Ligase

VHL Ligand-Linker Conjugates 15

Cat.No: T17908

Synonym: E3 Ligase Ligand-Linker Conjugates 56

Target: Others

(S,R,S)-AHPC-PEG4-NH2

Cat.No: T15190L

Synonym: VHL Ligand-Linker Conjugates 4,E3 ligase Ligand-Linker Conjugates 7 Free Base,VH032-PEG4-NH2

Target: Others, Ligand for E3 Ligase

Cat. No.	Product Name	Target	Signaling Pathways
T24729	Roseoflavin	Antibacterial	Microbiology/Virology
	Roseoflavin 是天然色素，起初分离自Streptomyces davawensis。Roseoflavin 是核黄素和黄素单核苷酸的抗代谢类似物，显示出抗菌活性。
TQ0176	(-)-Isocorypalmine Tetrahydrocolumbamine,(-)-异延胡索单酚碱,(S)-Tetrahydrocolumbamine	Dopamine Receptor; Antifungal	GPCR/G Protein; Microbiology/Virology; Neuroscience
	(-)-Isocorypalmine ((S)-Tetrahydrocolumbamine) 是一种多巴胺受体配体，从延胡索粗碱中分离得到。重组CYP719A21 对 (-)-Isocorypalmine 具有严格的底物特异性和高亲和力 (Km=4.63 μM)。
T8097	Methyl 3-aminopropanoate hydrochloride β-Alanine methyl ester hydrochloride,3-氨基丙酸甲酯盐酸盐	Others	Others
	Methyl 3-aminopropanoate hydrochloride (β-Alanine methyl ester hydrochloride) 是由 Β-Alanine (I) 酯化得到。它可用于合成双齿吡啶酸配体。
T14063	7α,25-Dihydroxycholesterol 7α,25-OHC	EBI2/GPR183; Endogenous Metabolite	GPCR/G Protein; Metabolism
	7α,25-Dihydroxycholesterol 是一种孤儿 GPCR 受体EBI2 (GPR183)的内源性配体和有效选择性激动剂。它对激活 EBI2 有很强的作用 (EC50=140 pM;Kd=450 pM)。它能够作为一种趋化因子，指导 B 细胞、T 细胞和树突状细胞的迁移。
T4S0039	Baimaside 白麻苷,Quercetin-3-O-sophoroside,Quercetin 3-beta-D-sophoroside	Others	Others
	Baimaside (Quercetin-3-O-sophoroside) 是一种超氧阴离子的清除剂，分离自A. venetum 的花中。
TN1023	Miltirone	P450; GABA Receptor	Membrane transporter/Ion channel; Metabolism; Neuroscience
	Miltirone 是存在于丹参中的一种天然产物，可作为中枢苯二氮受体部分激动剂，IC50值为 0.3 μM。
TP1232L	Amylin, amide, rat acetate(124447-81-0,free base)	Amylin Receptor	GPCR/G Protein
	Amylin, amide, rat acetate(124447-81-0,free base) 是 AMY1 和 AMY3 受体以及 AMY2 受体的强效和高亲和力配体。
TN2077	(+/-)-Pinocembrin NSC 43318,(±)-5,7-Dihydroxyflavanone	GPR; Others	Endocrinology/Hormones; GPCR/G Protein; Others
	(+/-)-Pinocembrin (NSC-43318) 是一种来自腋松的天然产物，它是一种 GPR120 配体，能促进 HaCaT 细胞系的伤口愈合。
T3806	kaempferide Kaempferol 4'-O-methyl ether,山奈素,Kaempferol 4'-methyl ether,4'-Methylkaempferol,4'-O-Methylkaempferol	Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Influenza Virus; Antibacterial; Autophagy	Autophagy; Endocrinology/Hormones; Microbiology/Virology
	kaempferide (4'-Methylkaempferol) 是一种存在于山柰中的O-甲基化黄酮醇，具有抗病毒活性。
T13815	Penicillic acid	Apoptosis; Caspase; Antibacterial; Antibiotic	Apoptosis; Microbiology/Virology; Proteases/Proteasome
	Penicillic acid, a polyketide mycotoxin, synthesized by various species of Aspergillus and Penicillium, acts as an inhibitor of Fas ligand-induced apoptosis by impeding self-processing of caspase-8. Additionally, in vitro studies have shown that Penicillic acid displays cytotoxic properties in rat alveolar macrophages.
T8363	DL-Serine	PKM	Metabolism
	DL-Serine 是 D-丝氨酸和 L-丝氨酸的混合物，是一种基础代谢物。它具有抗病毒作用，能抑制烟草花叶病毒的增殖。
Fr12596	3-Acetylcoumarin	Others	Others
	3-Acetylcoumarin 作为室温下铜催化 CN 偶联反应的实用配体。它具有神经保护和杀螨特性。
T5026	Oxytocin 催产素,α-Hypophamine,Oxytocic hormone,Oxytocin (Syntocinon)	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	Oxytocin (Oxytocin (Syntocinon)) 是哺乳动物的神经垂体激素，是多效的下丘脑肽，是催产素受体的配体，有助于分娩、哺乳和亲社会行为。它可作为一种压力应对分子，具有抗炎、抗氧化剂和保护作用。
TJS1183	Cyclen 轮环藤宁,1,4,7,10-tetraazacyclododecane	Others	Others
	Cyclen (1,4,7,10-tetraazacyclododecane) 是一种氮杂冠醚的类似物，是制备有效的大环螯合物的中间体，是制备磁共振造影剂的前体物质。
TN3209	3′,4′,7-Trihydroxyflavone	ATPase; Others; p38 MAPK; NF-κB	MAPK; Membrane transporter/Ion channel; NF-κB; Others
	3',4',7-Trihydroxyflavone 是分离自蚕豆荚的黄酮苷元化合物。
T5145	Oxytocin acetate Oxytocic hormone acetate,α-Hypophamine acetate,Oxytocin acetate (50-56-6 free base),醋酸催产素	Oxytocin Receptor	Endocrinology/Hormones; GPCR/G Protein
	Oxytocin acetate (α-Hypophamine acetate) 是哺乳动物的神经垂体激素，是多效的下丘脑肽，是催产素受体的配体，有助于分娩、哺乳和亲社会行为。它可作为一种压力应对分子，具有抗炎、抗氧化剂和保护作用。
T3S0738	yangonin Y100550,甲氧醉椒素	Cannabinoid Receptor; NF-κB; Autophagy	Autophagy; GPCR/G Protein; NF-κB
	Yangonin (Y100550) 是一种新型 CB1 受体配体，对人重组 CB1 受体具有亲和力。它可能是干预 NF-κB 依赖性病理状况的候选药物。
T36857	Estrone sulfate sodium 雌酮3-硫酸钠,Estrone 3-sulfate (sodium salt),17β-Estrone 3-sulfate	Endogenous Metabolite	Metabolism
	Estrone sulfate sodium (17β-Estrone 3-sulfate) 是一种主要的循环血浆雌激素，无生物活性，通过类固醇硫酸酯酶(STS) 转化为生物活性雌激素雌酮。
T15705	Laminaran β-1,3-Glucan
	Laminaran 是一种从褐藻中分离出来的 β-1-3-葡聚糖，常作为 Dectin-1 的典型配体，具有抗癌、免疫调节和辐射防护作用。 Laminaran 可被葡糖酶催化。Laminaran 在体内外实验中显示出抗肿瘤活性，可用于预防和治疗癌症。
T7998	1,7-Diaminoheptane	Others	Others
	1,7-Diaminoheptane 是一种脂族胺家族的化合物。它可用于合成肽、拟肽和其他化合物，也被用作酶反应中的底物，金属配合物中的配体，以及有机合成中的试剂。
TN2143	3,7,4'-Trihydroxyflavone Resokaempferol,5-Deoxykampferol	DNA	DNA Damage/DNA Repair
	3,7,4'-Trihydroxyflavone(5-Deoxykampferol) 是从黄檀心材中分离得到的一种具有 DNA 断链活性的黄酮类化合物，可抑制 NF-κB 配体（RANKL）受体激活剂诱导的 RAW 264.7 细胞和骨髓巨噬细胞中的破骨细胞分化、肌动蛋白环形成和骨吸收。
T4973	Paraxanthine 1,7-二甲基黄嘌呤,1,7-DIMETHYLXANTHINE	Endogenous Metabolite	Metabolism
	Paraxanthine (1,7-dimethylxanthine) 是一种 caffeine 的代谢物，能够刺激Ryanodine 受体通道来抑制多巴胺能细胞的死亡。
TL0005	3,5-O-Dicaffeoylquinic acid Isochlorogenic Acid A,(-)-3,5-二咖啡酰奎宁酸,(-)-3,5-Dicaffeoyl quinic acid,3,5-Dicaffeoylquinic Acid	Others	Others
	3,5-O-Dicaffeoylquinic acid (Isochlorogenic Acid A) 能够改善由三甲基锡诱导的学习和记忆缺陷。
T0034	Cortisone acetate 醋酸可的松,Cortisone 21-acetate,NSC 49420	Glucocorticoid Receptor; Endogenous Metabolite	Endocrinology/Hormones; Metabolism
	Cortisone acetate (NSC-49420) 是 Cortisol(一种糖皮质激素)的氧化代谢产物。它在高浓度下能够部分干预 Glucocorticoid 与Glucocorticoid-receptor 的结合。它具有免疫抑制和消炎的作用。
TN6694	5,6-Benzoflavone β-Naphthoflavone,beta-NF	Antioxidant	oxidation-reduction
	5,6-Benzoflavone (β-Naphthoflavone) 是芳烃受体的外源配体，可破坏人肝癌 HepG2 细胞中的锌稳态。5,6-Benzoflavone (β-Naphthoflavone) 具有抗炎和抗氧化活性，抑制通过 AKT/Nrf-2/HO-1-NF-kappaB 信号转导轴，抑制 LPS 诱导的炎症，抑制TNF-α诱导的ICAM-1和VCAM-1表达，可用于研究神经退行性疾病。
T2915	Bardoxolone RTA 401,齐墩果烷三萜化合物,CDDO	Others; Nrf2	Immunology/Inflammation; Others
	Bardoxolone (CDDO) 是新型核调节因子激活剂。
T1168	Desonide Tridesilon,地索奈德,Locapred,Prednacinolone	Glucocorticoid Receptor	Endocrinology/Hormones
	Desonide (Prednacinolone) 是一种非氟化皮质类固醇抗炎剂，能够作用于糖皮质激素受体。
T4S0498	Glaucocalyxin A 蓝萼甲素,Wangzaozin B,Leukamenin F	Apoptosis; Akt; Caspase; PI3K	Apoptosis; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Proteases/Proteasome
	Glaucocalyxin A (Leukamenin F) 是来自日本黑纹病菌的一种对映型月桂基二萜，具有抗肿瘤作用。它通过调节PI3K/Akt 信号通路抑制 GLI1 的核易位，诱导骨肉瘤凋亡。
T37974	(S)-Coriolic acid 13(S)-HODE	Lipoxygenase; Mitochondrial Metabolism; PPAR	DNA Damage/DNA Repair; Metabolism
	(S)-Coriolic acid (13(S)-HODE) 是一种重要的细胞内信号剂，是亚油酸与植物和哺乳动物脂氧合酶反应生成的，在各种生物系统中参与细胞增殖和分化。(S)-Coriolic acid 在 1 μM 左右时，它能抑制肿瘤细胞与血管内皮的粘附，能下调 IRGpIIb/IIIa 受体的表达。(S)-Coriolic acid 是15-脂氧合酶 (15-LOX) 代谢产物，常作为内源性配体激活 PPARγ。(S)-Coriolic acid 诱导线粒体功能障碍和气道上皮损伤。
T0798	Triamcinolone Fluoxyprednisolone,曲安西龙,Aristocort,Rodinolone	Glucocorticoid Receptor; COX	Endocrinology/Hormones; Immunology/Inflammation; Neuroscience
	Triamcinolone (Aristocort) 是一种皮质类固醇激素受体激动剂，也是一种合成的长效糖皮质激素，具有抗炎活性。
T14011	2-Arachidonoylglycerol	Cannabinoid Receptor; Endogenous Metabolite	GPCR/G Protein; Metabolism
	2-Arachidonoylglycerol 属于人内源性代谢物，是中枢神经系统中的一种内源性大麻素配体。
T4938	Potassium 1H-indol-3-yl sulfate 硫酸吲哚钾盐,Indoxyl sulfate potassium salt,Potassium 3-indoxyl sulfate	AhR; Endogenous Metabolite	Immunology/Inflammation; Metabolism
	Potassium 1H-indol-3-yl sulfate (Potassium 3-indoxyl sulfate) 是人芳烃受体(AhR)的激动剂。芳烃受体(AhR)最近被发现是免疫炎症条件的病理生理调节剂，Potassium 1H-indol-3-yl sulfate 已被证明是AhR的配体。Potassium 1H-indol-3-yl sulfate 也是膳食蛋白质中色氨酸的代谢物。色氨酸被肠道细菌代谢为吲哚，吲哚被吸收到血液中，然后在肝脏中进一步代谢为硫酸吲哚，通常通过尿液排出体外。在肾功能受损的慢性肾病患者中，Potassium 1H-indol-3-yl sulfate 可作为尿毒症毒素在血清中积累，诱导氧化应激并加速疾病进展。250 μM Potassium 1H-indol-3-yl sulfate 可诱导NF-Κb活化，促进大鼠近端小管细胞TGF-β1和Smad3的表达，与促纤维化活性相关。
T13735	Imidazoleacetic acid Imidazolyl-4-acetic acid	Others	Others
	Imidazoleacetic acid, an endogenous ligand, stimulates imidazole receptors.
T38468	Glycodeoxycholic acid monohydrate
	Glycodeoxycholic acid monohydrate is a nuclear receptor ligand.
T10821	Cirsiliol	Lipoxygenase	Metabolism
	Cirsiliol is a selective inhibitor of 5-lipoxygenase and a competitive low-affinity ligand of benzodiazepine receptors.
T16846	Sauristolactam Saurolactam	Others	Others
	Sauristolactam inhibits the receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclastogenesis and has the potential to inhibit osteoclast differentiation. Sauristolactam, a natural aristolactam isolated from aerial portions of Saururus Chi
TN4628	Nelumol A	FXR	Metabolism
	Nelumol A, and nelumal A show a potency comparable to the endogenous ligand, they may as a valuable potential novel lead compound in the search for FXR agonists.
TN1484	Cheilanthifoline	NF-κB; Antifection	Microbiology/Virology; NF-κB
	Cheilanthifoline has anti-osteoclastogenic property, it gives significant inhibitions on receptor activator of nuclear factor-κB ligand-induced differentiation of mouse bone marrow-derived macrophages into multinucleated osteoclasts.
T75682	Cortisol sulfate
	Cortisol sulfate (Cortisol 21-sulfate) 是皮质醇的一种代谢物。Cortisol sulfate 是细胞内运皮质激素蛋白的一种特异性配体。
T82578	Desacetylxanthanol
	Desacetylxanthanol (Compound 4)，源自Xanthium strumarium的倍半萜类化合物，展现出抗肿瘤坏死因子相关凋亡诱导配体(TRAIL)活性。
T21577	Narasin (sodium salt) Naracin sodium salt,naransin sodium,海南霉素,HainanMycin	NF-κB	NF-κB
	Narasin (sodium salt) (HainanMycin) 通过神经胶质瘤细胞中的 ER 应激诱导肿瘤坏死因子相关凋亡诱导配体 (TRAIL) 介导的细胞凋亡，并通过抑制 IκBα 的磷酸化来抑制 NF-κB 信号传导。
TN3537	Braylin	IL Receptor; TNF; NF-κB	Apoptosis; Immunology/Inflammation; NF-κB
	Braylin has anti-inflammatory, antinociceptive and immunomodulatory effects, which possibly act through the glucocorticoid receptor activation and by inhibition of the transcriptional activity of NF-ÎºB. Braylin is also a phosphodiesterase-4 inhibitor, it could represent an ideal prototype of glucocorticoid receptor ligand, able to induce synergic immunomodulatory effects.
T21500	Sphingosine-1-phosphate S1P	Endogenous Metabolite; S1P Receptor; LPL Receptor	GPCR/G Protein; Metabolism
	Sphingosine-1-phosphate (S1P) 是 S1P1-5 受体 (S1P1-5 receptors) 的激动剂和 GPR3、GPR6、GPR12 的配体。Sphingosine-1-phosphate 是细胞内的第二信使，动员 Ca2+ 作为 G 蛋白偶联受体的细胞外配体。Sphingosine-1-phosphate 是由鞘磷脂 (HY-113498) 或其他膜磷脂生成的重要脂质介质。
T82572	D-Glucosyl-β-1,1′-N-palmitoylsphingosine C16 Glucosyl(β) Ceramide (d18:1/16:0)
	D-Glucosyl-β-1,1′-N-palmitoylsphingosine (C16 Glucosyl(β) Ceramide (d18:1/16:0)) 是内源性Mincle配体，具免疫刺激活性。
TN4383	Kazinol U	IL Receptor; IκB/IKK; NOS; NF-κB	Immunology/Inflammation; NF-κB
	Kazinol U may have therapeutic value in delaying pancreatic β-cell destruction in type 1 diabetes by blocking the NF-ÎºB pathway in pancreatic β-cells reduces cell damage. Kazinol U shows estrogenic activity with ligand-activity of estrogen receptor, transcriptional activity of estrogen -responsive element-reporter genes, it may have beneficial effects in the treatment of menopausal symptoms.
TN3539	Broussonin A	ERK; IL Receptor; IκB/IKK; NOS; NF-κB; Akt	Cytoskeletal Signaling; Immunology/Inflammation; MAPK; NF-κB; PI3K/Akt/mTOR signaling
	Broussonins A and B, new phytoalexins from diseased paper mulberry. Broussonin A shows estrogenic activity with ligand-binding activity of estrogen receptor, transcriptional activity of estrogen-responsive element-luciferase reporter genes. Broussonin A c
T36563	(E)-Guggulsterone
	Bile acids are essential for solubilization and transport of dietary lipids, are the major products of cholesterol catabolism, and are physiological ligands for farnesoid X receptor (FXR), a nuclear receptor that regulates genes involved in lipid metabolism.1They are also inherently cytotoxic, as physiological imbalance contributes to increased oxidative stress.2,3Bile acid-controlled signaling pathways are promising novel targets to treat such metabolic diseases as obesity, type II diabetes, hy...

天然产物

Cat.No: T24729

Target: Antibacterial

(-)-Isocorypalmine

Cat.No: TQ0176

Synonym: Tetrahydrocolumbamine,(-)-异延胡索单酚碱,(S)-Tetrahydrocolumbamine

Target: Dopamine Receptor, Antifungal

Methyl 3-aminopropanoate hydrochloride

Cat.No: T8097

Synonym: β-Alanine methyl ester hydrochloride,3-氨基丙酸甲酯盐酸盐

Target: Others

7α,25-Dihydroxycholesterol

Cat.No: T14063

Synonym: 7α,25-OHC

Target: EBI2/GPR183, Endogenous Metabolite

Cat.No: T4S0039

Synonym: 白麻苷,Quercetin-3-O-sophoroside,Quercetin 3-beta-D-sophoroside

Target: Others

Cat.No: TN1023

Target: P450, GABA Receptor

Amylin, amide, rat acetate(124447-81-0,free base)

Cat.No: TP1232L

Target: Amylin Receptor

(+/-)-Pinocembrin

Cat.No: TN2077

Synonym: NSC 43318,(±)-5,7-Dihydroxyflavanone

Target: GPR, Others

Cat.No: T3806

Synonym: Kaempferol 4'-O-methyl ether,山奈素,Kaempferol 4'-methyl ether,4'-Methylkaempferol,4'-O-Methylkaempferol

Target: Estrogen Receptor/ERR, Estrogen/progestogen Receptor, Influenza Virus, Antibacterial, Autophagy

Penicillic acid

Cat.No: T13815

Target: Apoptosis, Caspase, Antibacterial, Antibiotic

Cat.No: T8363

Target: PKM

3-Acetylcoumarin

Cat.No: Fr12596

Target: Others

Cat.No: T5026

Synonym: 催产素,α-Hypophamine,Oxytocic hormone,Oxytocin (Syntocinon)

Target: Oxytocin Receptor

Cat.No: TJS1183

Synonym: 轮环藤宁,1,4,7,10-tetraazacyclododecane

Target: Others

3′,4′,7-Trihydroxyflavone

Cat.No: TN3209

Target: ATPase, Others, p38 MAPK, NF-κB

Oxytocin acetate

Cat.No: T5145

Synonym: Oxytocic hormone acetate,α-Hypophamine acetate,Oxytocin acetate (50-56-6 free base),醋酸催产素

Target: Oxytocin Receptor

Cat.No: T3S0738

Synonym: Y100550,甲氧醉椒素

Target: Cannabinoid Receptor, NF-κB, Autophagy

Estrone sulfate sodium

Cat.No: T36857

Synonym: 雌酮3-硫酸钠,Estrone 3-sulfate (sodium salt),17β-Estrone 3-sulfate

Target: Endogenous Metabolite

Cat.No: T15705

Synonym: β-1,3-Glucan

1,7-Diaminoheptane

Cat.No: T7998

Target: Others

3,7,4'-Trihydroxyflavone

Cat.No: TN2143

Synonym: Resokaempferol,5-Deoxykampferol

Target: DNA

Cat.No: T4973

Synonym: 1,7-二甲基黄嘌呤,1,7-DIMETHYLXANTHINE

Target: Endogenous Metabolite

3,5-O-Dicaffeoylquinic acid

Cat.No: TL0005

Synonym: Isochlorogenic Acid A,(-)-3,5-二咖啡酰奎宁酸,(-)-3,5-Dicaffeoyl quinic acid,3,5-Dicaffeoylquinic Acid

Target: Others

Cortisone acetate

Cat.No: T0034

Synonym: 醋酸可的松,Cortisone 21-acetate,NSC 49420

Target: Glucocorticoid Receptor, Endogenous Metabolite

5,6-Benzoflavone

Cat.No: TN6694

Synonym: β-Naphthoflavone,beta-NF

Target: Antioxidant

Cat.No: T2915

Synonym: RTA 401,齐墩果烷三萜化合物,CDDO

Target: Others, Nrf2

Cat.No: T1168

Synonym: Tridesilon,地索奈德,Locapred,Prednacinolone

Target: Glucocorticoid Receptor

Glaucocalyxin A

Cat.No: T4S0498

Synonym: 蓝萼甲素,Wangzaozin B,Leukamenin F

Target: Apoptosis, Akt, Caspase, PI3K

(S)-Coriolic acid

Cat.No: T37974

Synonym: 13(S)-HODE

Target: Lipoxygenase, Mitochondrial Metabolism, PPAR

Cat.No: T0798

Synonym: Fluoxyprednisolone,曲安西龙,Aristocort,Rodinolone

Target: Glucocorticoid Receptor, COX

2-Arachidonoylglycerol

Cat.No: T14011

Target: Cannabinoid Receptor, Endogenous Metabolite

Potassium 1H-indol-3-yl sulfate

Cat.No: T4938

Synonym: 硫酸吲哚钾盐,Indoxyl sulfate potassium salt,Potassium 3-indoxyl sulfate

Target: AhR, Endogenous Metabolite

Imidazoleacetic acid

Cat.No: T13735

Synonym: Imidazolyl-4-acetic acid

Target: Others

Glycodeoxycholic acid monohydrate

Cat.No: T38468

Cat.No: T10821

Target: Lipoxygenase

Cat.No: T16846

Synonym: Saurolactam

Target: Others

Cat.No: TN4628

Target: FXR

Cheilanthifoline

Cat.No: TN1484

Target: NF-κB, Antifection

Cortisol sulfate

Cat.No: T75682

Desacetylxanthanol

Cat.No: T82578

Narasin (sodium salt)

Cat.No: T21577

Synonym: Naracin sodium salt,naransin sodium,海南霉素,HainanMycin

Target: NF-κB

Cat.No: TN3537

Target: IL Receptor, TNF, NF-κB

Sphingosine-1-phosphate

Cat.No: T21500

Synonym: S1P

Target: Endogenous Metabolite, S1P Receptor, LPL Receptor

D-Glucosyl-β-1,1′-N-palmitoylsphingosine

Cat.No: T82572

Synonym: C16 Glucosyl(β) Ceramide (d18:1/16:0)

Cat.No: TN4383

Target: IL Receptor, IκB/IKK, NOS, NF-κB

Cat.No: TN3539

Target: ERK, IL Receptor, IκB/IKK, NOS, NF-κB, Akt

(E)-Guggulsterone

Cat.No: T36563

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