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Search Results for " ligand for e3 ligase "

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Cat. No.	Product Name	Target	Signaling Pathways
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。
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。
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。
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。
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。
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。
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.
T7755	Thalidomide 4-fluoride E3 ligase Ligand 4,2-(2,6-二氧代-哌啶-3-基)-4-氟基-异吲哚-1,3-二酮	IRAK; Ligand for E3 Ligase	Immunology/Inflammation; NF-κB; PROTAC
	Thalidomide 4-fluoride (E3 ligase Ligand 4) 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 IRAK4 靶蛋白配体连接，得到 PROTAC IRAK4 degrader-1。
T22922	Lenalidomide hemihydrate	TNF; Ligand for E3 Ligase; Molecular Glues	Apoptosis; PROTAC
	Lenalidomide hemihydrate 是 Thalidomide 的衍生物，也是具有口服活性免疫调节剂，以分子胶的方式作用。它是泛素 E3 连接酶 cereblon 的配体，通过 CRBN-CRL4 泛素连接酶对两种淋巴转录因子 IKZF1 和 IKZF3 进行选择性泛素化和降解。
T8412	(S,R,S)-AHPC VH032-NH2,MDK7526,VHL ligand 1	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC (VH032-NH2) 是一种 VH032-based VHL ligand，可用于募集 von Hippel-Lindau (VHL)蛋白。它能够利用 linker 与靶蛋白配体连接，得到 PROTAC 分子。
T1642	Lenalidomide 来那度胺,CC-5013	Apoptosis; TNF; Ligand for E3 Ligase; Molecular Glues	Apoptosis; PROTAC
	Lenalidomide (CC-5013) 是 Thalidomide 的衍生物，也是具有口服活性免疫调节剂，以分子胶的方式作用。它是泛素 E3 连接酶 cereblon (CRBN) 的配体，可通过 CRBN-CRL4 泛素连接酶对两种淋巴转录因子 IKZF1 和 IKZF3 进行选择性泛素化和降解。
T17927	(S,R,S)-AHPC TFA VH032-NH2 TFA,VHL ligand 1 TFA	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC TFA (VHL ligand 1 TFA) 是一种 VH032-based VHL ligand，可用于募集 von Hippel-Lindau (VHL)蛋白。它能够利用 linker 与靶蛋白配体连接，形成 PROTAC 分子。
T9381	Thalidomide 5-fluoride 2-(2,6-二氧代 - 哌啶-3-基)-5-氟 - 异吲哚-1,3-二酮,H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-5-fluoro-	Ligand for E3 Ligase	PROTAC
	Thalidomide 5-fluoride (H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-5-fluoro-) 是一种基于沙利度胺的 Cereblon 配体，通过 linker 与 IRAK4 蛋白配体结合形成 PROTACIRAK4 degrader-1。
T4207	(S,R,S)-AHPC hydrochloride VHL Ligand 1 hydrochloride,ULM-1,Protein degrader 1 hydrochloride	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC hydrochloride (Protein degrader 1 hydrochloride) 是基于 VH032 的 VHL 配体，可用于募集 von Hippel-Lindau (VHL) 蛋白。它能够利用 linker 与靶蛋白配体连接，得到 PROTAC 分子。
T77912	Tz-Thalidomide	Epigenetic Reader Domain	Chromatin/Epigenetic
	Tz-Thalidomide 是一种四嗪修饰的 Thalidomide(E3连接酶配体),对 BRD4 具有一定的亲和力。
T18816	Thalidomide-O-amido-C6-NH2 hydrochloride	Others; E3 Ligase Ligand-Linker Conjugate	Others; PROTAC
	Thalidomide-O-amido-C6-NH2 hydrochloride 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，。它可用于 PROTAC 分子的合成。
T17881	(S,R,S)-AHPC-C10-NH2 VH032-C10-NH2	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-C10-NH2 (VH032-C10-NH2) 包含基于 (S,R,S)-AHPC 的VHL 配体和 1 个 linker，是一种合成的 E3 连接酶配体-linker 偶联物 (E3 ligase ligand-linker conjugate)。用于 BET 的靶向 PROTAC 的合成。
T18064	Lenalidomide-Br	Ligand for E3 Ligase	PROTAC
	Lenalidomide-Br (Compound 41) is a derivative of Lenalidomide, which serves as a ligand for cereblon (CRBN) - an E3 ubiquitin ligase involved in protein recruitment. This compound, Lenalidomide-Br, can be conjugated to a protein ligand through a linker to create PROTACs. For instance, Lenalidomide-Br is utilized as a component in the PROTAC STAT3 degrader SD-36.
T18066	Lenalidomide-OH	Ligand for E3 Ligase	PROTAC
	Lenalidomide-OH is a ligand of cereblon (CRBN), serving as an analog to Lenalidomide for E3 ubiquitin ligase. It is utilized in the recruitment of CRBN protein. Additionally, Lenalidomide-OH can be conjugated to a protein ligand through a linker, resulting in the formation of PROTACs. An example of a PROTAC BTK degrader incorporating Lenalidomide-OH is SJF620.
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。
T40019	Thalidomide-5-NH2-CH2-COOH	Others	Others
	Thalidomide-5-NH2-CH2-COOH (compound 114) 是原肌球蛋白受体激酶的选择性抑制剂。它是 E3 连接酶的配体，具有研究一种或多种疾病的潜力。
T18819	Thalidomide-O-amido-PEG2-C2-NH2 hydrochloride	Others; Ligand for E3 Ligase	Others; PROTAC
	Thalidomide-O-amido-PEG2-C2-NH2 hydrochloride 包含一个 E3 连接酶配体和一个 linker。 Thalidomide-O-amido-PEG2-C2-NH2 盐酸盐可用作治疗癌症的免疫调节剂。
T17350	ACBI1	Apoptosis; Epigenetic Reader Domain; PROTACs	Apoptosis; Chromatin/Epigenetic; PROTAC
	ACBI1 是一种基于PROTAC 技术的 BAF ATPase 亚基SMARCA2和SMARCA4降解剂，也是 PBAF 成员PBRM1的降解剂。它由一个 bromodomain 配体、linker 和 E3 泛素连接酶von Hippel-Lindau 构成，能诱导抗增殖作用和凋亡。
T41224	CG 428	Trk receptor	Tyrosine Kinase/Adaptors
	CG 428 是一种有效的原肌球蛋白受体激酶 (TRK) 降解剂 (uSMITETM)，DC50 为 0.36 nM。 CG 428 包含泛 TRK 抑制剂 GNF-8625 的类似物，通过接头连接到 cereblon E3 连接酶配体泊马度胺。 CG 428 对 TRKA 的选择性优于 TRKC 和 TRKB，Kd 为 1nM、4.2 nM 和 28 nM。 CG 428 抑制 KM12 结肠癌细胞的生长，IC50 为 2.9 nM。
T17871	E3 ligase Ligand 13	Others	Others
	E3 ligase Ligand 13 is an E3 ubiquitin ligase ligand that can be employed to create PROTACs, which are connected to the ligand for the protein through a linker. PROTACs serve as inducers of ubiquitination-mediated degradation of cancer-promoting proteins[1].
T17364	AhR Ligand-Linker Conjugates 1 E3 Ligase Ligand-Linker Conjugates 57	Others	Others
	AhR Ligand-Linker Conjugates 1, also known as E3 Ligase Ligand-Linker Conjugates 57, is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase with a SNIPER linker. It is specifically designed to be used in the development of SNIPER[1].
T35479	CRBN-6-5-5-VHL
	Potent and selective cereblon degrader (DC50 = 1.5 nM). Induces complete degradation of cereblon in MM1S cells. Comprises a cereblon E3 ligase ligand joined by a linker to a ligand for the E3 ligase VHL. Cell-permeable. Steinebach et al (2019) PROTAC-mediated crosstalk between E3 ligases. Chem.Commun.(Camb) 55 1821 PMID:30672516
T17868	E3 ligase Ligand 10	Others	Others
	E3 ligase Ligand 10 serves as a ligand for E3 ubiquitin ligase and can be conjugated to a protein ligand through a linker, resulting in the formation of PROTACs. These PROTACs act as inducers of ubiquitination-mediated degradation, specifically targeting cancer-promoting proteins[1].
T17880	E3 ligase Ligand 9	Others	Others
	E3 ligase Ligand 9 is a compound that serves as a ligand for E3 ubiquitin ligase. It can be linked to the protein ligand through a linker, forming PROTACs or SNIPERs. These PROTACs are known to induce the degradation of cancer-promoting proteins through ubiquitination-mediated mechanisms[1].
T18812	Thalidomide-PEG2-C2-NH2 TFA Thalidomide-NH-PEG2-C2-NH2 TFA	Others	Others
	Thalidomide-O-amido-PEG3-C2-NH2 TFA, a synthesized E3 ligase ligand-linker conjugate, combines the cereblon ligand based on Thalidomide and a 2-unit PEG linker for use in PROTAC technology[1].
T39931	(S,R,S)-AHPC-C8-NH2 hydrochloride (S,R,S)-AHPC-C8-NH2 hydrochloride,VH032-C8-NH2 hydrochloride
	'(S,R,S)-AHPC-C8-NH2 (VH032-C8-NH2) hydrochloride is a synthetic E3 ligase ligand-linker conjugate, consisting of the VH032-based VHL ligand and a linker for use in PROTAC technology.'
T18826	Thalidomide-O-PEG2-propargyl E3 ligase Ligand-Linker Conjugates 32	Others	Others
	Thalidomide-O-PEG2-propargyl (E3 Ligase Ligand-Linker Conjugates 32) is a chemical compound that has been synthesized as a conjugate of an E3 ligase ligand and a linker. It incorporates the cereblon ligand based on Thalidomide, along with a 2-unit PEG linker. This compound is specifically designed for use in PROTAC technology, which utilizes ligand-induced protein degradation [1].
T17897	cIAP1 Ligand-Linker Conjugates 13 E3 ligase Ligand-Linker Conjugates 43	Others	Others
	cIAP1 Ligand-Linker Conjugates 13, containing an IAP ligand for the E3 ubiquitin ligase, and a PROTAC linker, are utilized in the development of SNIPERs[1].
T39378	Thalidomide-O-C10-NH2 Thalidomide-O-C10-NH2
	Thalidomide-O-C10-NH2 is a synthetic E3 ligase ligand-linker conjugate combining a cereblon ligand derived from Thalidomide with a linker crucial for PROTAC technology.
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].
T17900	cIAP1 Ligand-Linker Conjugates 8 E3 ligase Ligand-Linker Conjugates 46	Others	Others
	cIAP1 Ligand-Linker Conjugates 8 comprises an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. This compound is specifically utilized for the purpose of SNIPER design[1].
T39375	Thalidomide-O-amido-PEG2-C2-NH2 Cereblon Ligand-Linker Conjugates 10,E3LigaseLigand-LinkerConjugates24,Thalidomide-O-amido-PEG2-C2-NH2
	Thalidomide-O-amido-PEG2-C2-NH2, which combines an E3 ligase ligand with a linker, serves as an immunomodulator for cancer treatment.
T17899	cIAP1 Ligand-Linker Conjugates 9 E3 ligase Ligand-Linker Conjugates 45	Others	Others
	cIAP1 Ligand-Linker Conjugates 9 feature an IAP ligand specifically targeting the E3 ubiquitin ligase, along with a PROTAC linker. It is valuable tools for developing SNIPERs[1].
T17898	cIAP1 Ligand-Linker Conjugates 7 E3 ligase Ligand-Linker Conjugates 44	Others	Others
	cIAP1 Ligand-Linker Conjugates 7 is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase with a PROTAC linker. It is utilized in the design of SNIPERs[1].
T39736	(S,R,S)-AHPC-C2-NH2 (S,R,S)-AHPC-C2-NH2
	(S,R,S)-AHPC-C2-NH2 is a synthesized conjugate combining the VH032-based VHL ligand with a linker for PROTAC technology, serving as an E3 ligase ligand-linker.
T18673	(S,R,S)-AHPC-O-Ph-PEG1-NH2 VH032-O-Ph-PEG1-NH2	Others	Others
	(S,R,S)-AHPC-O-Ph-PEG1-NH2 (VH032-O-Ph-PEG1-NH2) serves as an E3 ligase ligand-linker conjugate, integrating a VHL ligand for the E3 ubiquitin ligase and a PROTAC linker. This compound is utilized in PROTAC EED degrader-1, a PROTAC that targets EED with a potency (pKD) of 9.02[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].
T39804	Pomalidomide-PEG3-azide Pomalidomide-PEG3-azide
	Pomalidomide-PEG3-azide is a chemically synthesized conjugate comprised of a cereblon ligand based on Pomalidomide, an E3 ligase ligand-linker, and a 3-unit PEG linker. This conjugate is specifically designed for use in PROTAC technology.
T17888	cIAP1 Ligand-Linker Conjugates 6 hydrochloride E3 ligase Ligand-Linker Conjugates 35 hydrochloride	Others	Others
	cIAP1 Ligand-Linker Conjugates 6 hydrochloride is a compound that combines an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. It is utilized for the purpose of designing SNIPERs[1].
T18633	PROTAC MDM2 Degrader-3	Others	Others
	PROTAC MDM2 Degrader-3 is a compound that leverages PROTAC technology to degrade MDM2. It consists of a highly effective MDM2 inhibitor, a linker, and the MDM2 ligand for E3 ubiquitin ligase[1].
T18811	Thalidomide-PEG2-C2-NH2 hydrochloride Thalidomide-NH-PEG2-C2-NH2 hydrochloride	Others	Others
	Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride, a synthesized E3 ligase ligand-linker conjugate, combines a Thalidomide-based cereblon ligand with a two-unit PEG linker for use in PROTAC technology[1].
T39876	Thalidomide 4'-oxyacetamide-alkyl-C2-amine hydrochloride Thalidomide 4'-oxyacetamide-alkyl-C2-amine hydrochloride
	Thalidomide 4'-oxyacetamide-alkyl-C2-amine hydrochloride consists of a cereblon (CRBN) ligand for the E3 ubiquitin ligase and a linker, making it suitable for PROTACs design.
T77965	DCAF1 binder 1
	DCAF1 binder 1 是针对 CRL4 DCAF1 E3 连接酶复合物的选择性 ligands for E3 Ligase，旨在用于靶向蛋白质降解 (TPD)。
T17886	cIAP1 Ligand-Linker Conjugates 15 hydrochloride E3 ligase Ligand-Linker Conjugates 34 hydrochloride	Others	Others
	cIAP1 Ligand-Linker Conjugates 15 hydrochloride is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase and a PROTAC linker. This compound is useful in the development of SNIPERs[1].
T39873	(S,R,S)-AHPC-C8-NH2 VH032-C8-NH2,(S,R,S)-AHPC-C8-NH2
	(S, R, S)-AHPC-C8-NH2 (VH032-C8-NH2) is an E3 ligase ligand-linker conjugate. This compound comprises the VH032-based VHL ligand and a linker, specifically designed for AKT PROTAC degrader applications.

化合物

E3 ligase Ligand 8

Cat.No: T17879

Target: Others, Ligand for E3 Ligase

E3 ligase Ligand 23

Cat.No: T9809

Target: Ligand for E3 Ligase

Thalidomide-4-OH

Cat.No: T7763

Synonym: Cereblon ligand 2,E3 ligase Ligand 2

Target: Ligand for E3 Ligase

(S,R,S)-AHPC-Me

Cat.No: T7752

Synonym: VHL ligand 2,E3 ligase Ligand 1A

Target: Ligand for E3 Ligase

Thalidomide-O-COOH

Cat.No: T7753

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

Target: Others, Ligand for E3 Ligase

VH032-cyclopropane-F

Cat.No: T17877

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

Target: Others, 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

Thalidomide 4-fluoride

Cat.No: T7755

Synonym: E3 ligase Ligand 4,2-(2,6-二氧代-哌啶-3-基)-4-氟基-异吲哚-1,3-二酮

Target: IRAK, Ligand for E3 Ligase

Lenalidomide hemihydrate

Cat.No: T22922

Target: TNF, Ligand for E3 Ligase, Molecular Glues

Cat.No: T8412

Synonym: VH032-NH2,MDK7526,VHL ligand 1

Target: Others, Ligand for E3 Ligase

Cat.No: T1642

Synonym: 来那度胺,CC-5013

Target: Apoptosis, TNF, Ligand for E3 Ligase, Molecular Glues

(S,R,S)-AHPC TFA

Cat.No: T17927

Synonym: VH032-NH2 TFA,VHL ligand 1 TFA

Target: Others, Ligand for E3 Ligase

Thalidomide 5-fluoride

Cat.No: T9381

Synonym: 2-(2,6-二氧代 - 哌啶-3-基)-5-氟 - 异吲哚-1,3-二酮,H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-5-fluoro-

Target: Ligand for E3 Ligase

(S,R,S)-AHPC hydrochloride

Cat.No: T4207

Synonym: VHL Ligand 1 hydrochloride,ULM-1,Protein degrader 1 hydrochloride

Target: Others, Ligand for E3 Ligase

Cat.No: T77912

Target: Epigenetic Reader Domain

Thalidomide-O-amido-C6-NH2 hydrochloride

Cat.No: T18816

Target: Others, E3 Ligase Ligand-Linker Conjugate

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

Cat.No: T17881

Synonym: VH032-C10-NH2

Target: Others, Ligand for E3 Ligase

Lenalidomide-Br

Cat.No: T18064

Target: Ligand for E3 Ligase

Lenalidomide-OH

Cat.No: T18066

Target: Ligand for E3 Ligase

cIAP1 ligand 1

Cat.No: T17870

Synonym: E3 ligase Ligand 12

Target: Others

Thalidomide-5-NH2-CH2-COOH

Cat.No: T40019

Target: Others

Thalidomide-O-amido-PEG2-C2-NH2 hydrochloride

Cat.No: T18819

Target: Others, Ligand for E3 Ligase

Cat.No: T17350

Target: Apoptosis, Epigenetic Reader Domain, PROTACs

Cat.No: T41224

Target: Trk receptor

E3 ligase Ligand 13

Cat.No: T17871

Target: Others

AhR Ligand-Linker Conjugates 1

Cat.No: T17364

Synonym: E3 Ligase Ligand-Linker Conjugates 57

Target: Others

Cat.No: T35479

E3 ligase Ligand 10

Cat.No: T17868

Target: Others

E3 ligase Ligand 9

Cat.No: T17880

Target: Others

Thalidomide-PEG2-C2-NH2 TFA

Cat.No: T18812

Synonym: Thalidomide-NH-PEG2-C2-NH2 TFA

Target: Others

(S,R,S)-AHPC-C8-NH2 hydrochloride

Cat.No: T39931

Synonym: (S,R,S)-AHPC-C8-NH2 hydrochloride,VH032-C8-NH2 hydrochloride

Thalidomide-O-PEG2-propargyl

Cat.No: T18826

Synonym: E3 ligase Ligand-Linker Conjugates 32

Target: Others

cIAP1 Ligand-Linker Conjugates 13

Cat.No: T17897

Synonym: E3 ligase Ligand-Linker Conjugates 43

Target: Others

Thalidomide-O-C10-NH2

Cat.No: T39378

Synonym: Thalidomide-O-C10-NH2

VHL Ligand-Linker Conjugates 15

Cat.No: T17908

Synonym: E3 Ligase Ligand-Linker Conjugates 56

Target: Others

cIAP1 Ligand-Linker Conjugates 8

Cat.No: T17900

Synonym: E3 ligase Ligand-Linker Conjugates 46

Target: Others

Thalidomide-O-amido-PEG2-C2-NH2

Cat.No: T39375

Synonym: Cereblon Ligand-Linker Conjugates 10,E3LigaseLigand-LinkerConjugates24,Thalidomide-O-amido-PEG2-C2-NH2

cIAP1 Ligand-Linker Conjugates 9

Cat.No: T17899

Synonym: E3 ligase Ligand-Linker Conjugates 45

Target: Others

cIAP1 Ligand-Linker Conjugates 7

Cat.No: T17898

Synonym: E3 ligase Ligand-Linker Conjugates 44

Target: Others

(S,R,S)-AHPC-C2-NH2

Cat.No: T39736

Synonym: (S,R,S)-AHPC-C2-NH2

(S,R,S)-AHPC-O-Ph-PEG1-NH2

Cat.No: T18673

Synonym: VH032-O-Ph-PEG1-NH2

Target: Others

cIAP1 Ligand-Linker Conjugates 5

Cat.No: T17893

Synonym: E3 ligase Ligand-Linker Conjugates 39

Target: Others

Pomalidomide-PEG3-azide

Cat.No: T39804

Synonym: Pomalidomide-PEG3-azide

cIAP1 Ligand-Linker Conjugates 6 hydrochloride

Cat.No: T17888

Synonym: E3 ligase Ligand-Linker Conjugates 35 hydrochloride

Target: Others

PROTAC MDM2 Degrader-3

Cat.No: T18633

Target: Others

Thalidomide-PEG2-C2-NH2 hydrochloride

Cat.No: T18811

Synonym: Thalidomide-NH-PEG2-C2-NH2 hydrochloride

Target: Others

Thalidomide 4'-oxyacetamide-alkyl-C2-amine hydrochloride

Cat.No: T39876

Synonym: Thalidomide 4'-oxyacetamide-alkyl-C2-amine hydrochloride

Cat.No: T77965

cIAP1 Ligand-Linker Conjugates 15 hydrochloride

Cat.No: T17886

Synonym: E3 ligase Ligand-Linker Conjugates 34 hydrochloride

Target: Others

(S,R,S)-AHPC-C8-NH2

Cat.No: T39873

Synonym: VH032-C8-NH2,(S,R,S)-AHPC-C8-NH2

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