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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。
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。
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。
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。
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。
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,。
T17924 (S,R,S)-AHPC-PEG2-NH2 hydrochloride

VH032-PEG2-NH2 hydrochloride,VHL Ligand-Linker Conjugates 3 hydrochloride,E3 ligase Ligand-Linker Conjugates 6

Others; E3 Ligase Ligand-Linker Conjugate Others; PROTAC
(S,R,S)-AHPC-PEG2-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 6) 包含基于 (S,R,S)-AHPC 的 VHL 配体和 2 个单元 PEG 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。
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。
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 ligand3-unit PEG linker。
T40002 Pomalidomide-C3-NH2 hydrochloride

Others; E3 Ligase Ligand-Linker Conjugate Others; PROTAC
Pomalidomide-C3-NH2 hydrochloride 包含基于 Pomalidomide 的 cereblon 配体和 1 个 linker,是合成的 E3 连接酶配体-linker 偶联物,可用于 PROTAC 的合成。
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。
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].
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].
T17876 E3 ligase Ligand 18

Others Others
E3 ligase Ligand 18 is a ligand that binds to E3 ubiquitin ligase, and it can be chemically attached to a protein ligand through a linker to create PROTACs. The resulting PROTACs function as inducers of ubiquitination-mediated degradation, targeting cancer-promoting proteins[1].
T17872 E3 ligase Ligand 14

Others Others
E3 ligase Ligand 14 is a ligand that binds to E3 ubiquitin ligase and can be conjugated to a protein ligand via a linker to create PROTACs. These PROTACs are capable of promoting ubiquitination-mediated degradation of cancer-promoting proteins[1].
T17894 cIAP1 Ligand-Linker Conjugates 3

E3 ligase Ligand-Linker Conjugates 40

Others Others
cIAP1 Ligand-Linker Conjugates 3 are chemical compounds comprising an IAP ligand designed specifically for the E3 ubiquitin ligase and a PROTAC linker. These conjugates, denoted as cIAP1 Ligand-Linker Conjugates 3, find utility in the design of SNIPERs, short for Specific and Non-genetic IAP-dependent Protein Erasers [1].
T9401 Thalidomide-NH-PEG1-NH2 hydrochloride

4-[(2-(2-Aminoethoxy)ethyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione HCl

E3 Ligase Ligand-Linker Conjugate PROTAC
Thalidomide-NH-PEG1-NH2 hydrochloride (4-[(2-(2-Aminoethoxy)ethyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione HCl) 包含基于 Thalidomide 的 cereblon 配体和 1 个 linker,是合成的 E3 连接酶配体-linker 偶联物,可用于 PROTAC 的合成。
T17915 Thalidomide-O-amido-PEG3-C2-NH2

Cereblon Ligand-Linker Conjugates 3,E3 Ligase Ligand-Linker Conjugates 14

Others Others
Thalidomide-O-amido-PEG3-C2-NH2 (Cereblon Ligand-Linker Conjugates 3) is an E3 ligase ligand-linker conjugate which is designed using Thalidomide-based cereblon ligand and a 3-unit PEG linker. This compound is synthesized specifically for utilization in PROTAC technology.
T17925 (S,R,S)-AHPC-PEG2-NH2

VH032-PEG2-NH2,VHL Ligand-Linker Conjugates 3,E3 ligase Ligand-Linker Conjugates 6 Free Base

Others; E3 Ligase Ligand-Linker Conjugate Others; PROTAC
(S,R,S)-AHPC-PEG2-NH2 (VHL Ligand-Linker Conjugates 3) 包含基于 (S,R,S)-AHPC 的 VHL 配体和 2 个单元 PEG 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。
T17883 Pomalidomide-PEG3-C2-NH2

Cereblon Ligand-Linker Conjugates 5,E3 ligase Ligand-Linker Conjugates 30

Others; PROTAC Linker Others; PROTAC
Pomalidomide-PEG3-C2-NH2 (Cereblon Ligand-Linker Conjugates 5) 是一种合成的 E3 连接酶配体-linker 偶联物,包含基于 Pomalidomide 的 cereblon 配体和 3 单元 PEG 的linker。
T17914 Thalidomide-O-amido-C3-COOH

Cereblon Ligand-Linker Conjugates 7,E3 ligase Ligand-Linker Conjugates 15

Others Others
Thalidomide-O-amido-C3-COOH is a synthesized conjugate of an E3 ligase ligand-linker compound that combines a cereblon ligand derived from Thalidomide with a linker commonly employed in PROTAC technology.
T18553 Pomalidomide-amido-PEG3-C2-NH2

Cereblon Ligand-Linker Conjugates 22,E3 ligase Ligand-Linker Conjugates 55

Others Others
Pomalidomide-amido-PEG3-C2-NH2, known as Cereblon Ligand-Linker Conjugates 22, is a synthesized E3 ligase ligand-linker conjugate designed for use in PROTAC technology. It consists of the Pomalidomide-based cereblon ligand and a 3-unit PEG linker. [1]
T9382 Thalidomide-NH-C2-PEG3-OH

H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-4-[[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl]amino]-

E3 Ligase Ligand-Linker Conjugate PROTAC
Thalidomide-NH-C2-PEG3-OH (H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-4-[[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl]amino]-) 包含基于 Thalidomide 的 cereblon 配体和 1 个 linker,是 E3 连接酶配体-linker 偶联物,可用于合成 PROTAC BCL-XL 降解剂 XZ739。
T17923 (S,R,S)-AHPC-PEG3-NH2

E3 ligase Ligand-Linker Conjugates 5 Free Base,VH032-PEG3-NH2,VHL Ligand-Linker Conjugates 1

Others Others
(S,R,S)-AHPC-PEG3-NH2 is a synthetic conjugate of an E3 ligase ligand-linker, incorporating the (S,R,S)-AHPC VHL ligand and a 3-unit PEG linker, which are utilized in PROTAC technology.
T40031 Thalidomide-O-C6-NH2 hydrochloride

4-((6-aminohexyl)oxy)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride,萨力多胺-O-C6-氨基盐酸盐

E3 Ligase Ligand-Linker Conjugate PROTAC
Thalidomide-O-C6-NH2 hydrochloride (4-((6-aminohexyl)oxy)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride) 是一种合成的E3 连接酶配体 -linker 偶联物,用于 PROTAC dTAG-13 的合成。其中 dTAG-13 是一种 FKBP12F36V 和 BET 的降解剂。
T17912 (S,R,S)-AHPC-(C3-​PEG)​2-​C6-​Cl

VHL Ligand-Linker Conjugates 11,E3 ligase Ligand-Linker Conjugates 11

Others Others
(S,R,S)-AHPC-(C3- PEG) 2- C6- Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker. (S,R,S)-AHPC-(C3- PEG) 2- C6- Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
T17882 Pomalidomide-PEG3-C2-NH2 (TFA)

Cereblon Ligand-Linker Conjugates 5 (TFA),E3 ligase Ligand-Linker Conjugates 30 (TFA),Pomalidomide-PEG3-C2-NH2 (TFA) (2093416-31-8 free base)

Others Others
Pomalidomide-PEG3-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Pomalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology.
T17875 Pomalidomide-C2-NH2

Cereblon Ligand-Linker Conjugates 15,4-[(2-Aminoethyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione

Others; Ligand for E3 Ligase Others; PROTAC
Pomalidomide-C2-NH2 (4-[(2-Aminoethyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione) 包含基于 Pomalidomide 的 cereblon 配体和 1 个 linker,是一种合成的 E3 连接酶配体-linker 偶联物,。
T40023 Pomalidomide-PEG3-CO2H

Thalidomide-NH-PEG3-propionic acid

E3 Ligase Ligand-Linker Conjugate PROTAC
Pomalidomide-PEG3-CO2H (Thalidomide-NH-PEG3-propionic acid) 是一种由 E3 连接酶配体和连接体组成的偶联物,结合了基于 Thalidomide 的 Cereblon 配体和 3 个单元 PEG Linker。
T40016 Thalidomide-NH-CH2-COOH

2-[[2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindol-4-yl]amino]acetic acid,(2-(2,6-Dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)glycine

Ligand for E3 Ligase PROTAC
Thalidomide-NH-CH2-COOH ((2-(2,6-Dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)glycine) 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。
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.
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].
T39494 (S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH

VH032-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH,(S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH

(S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH, also known as VH032-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH, is a conjugate compound comprising a ligand-linker that targets E3 ligase and, on one end, features a VHL ligand. It is employed in PROTAC technology applications.
T39215 Thalidomide-O-amido-C3-PEG3-C1-NH2

Thalidomide-O-amido-C3-PEG3-C1-NH2

Thalidomide-O-amido-C3-PEG3-C1-NH2 is a synthesized conjugate compound that serves as an E3 ligase ligand-linker. It features a cereblon ligand based on Thalidomide and a 3-unit PEG linker. This compound is specifically designed for use in PROTAC technology.
T17917 Thalidomide-O-amido-PEG1-(C1-​PEG)2-C2-NH2

E3 Ligase Ligand-Linker Conjugates 23 TFA,Cereblon Ligand-Linker Conjugates 12 TFA

Others Others
Thalidomide-O-amido-PEG1-(C1-PEG)2-C2-NH2 is a synthesized conjugate compound known as an E3 ligase ligand-linker. It incorporates a cereblon ligand based on Thalidomide and a 3-unit PEG linker. This compound is specifically designed for use in PROTAC technology applications.
T17902 Nutlin-C1-amido-PEG4-C2-N3

E3 ligase Ligand-Linker Conjugates 48,MDM2 Ligand-Linker Conjugates 1

Others Others
Nutlin-C1-amido-PEG4-C2-N3 is a novel compound that functions as a ligand-linker conjugate for the E3 ligase. It is a synthesized molecule incorporating the MDM2 ligand derived from Nutlin 3, and a 4-unit PEG linker. This compound is specifically designed for utilization in PROTAC technology.
T41198 BRD PHOTAC-I-3

BRD PHOTAC-I-3 is a photoswitchable BET bromodomain degrader (PHOTAC, PHOtochemically TArgeting Chimera). BRD PHOTAC-I-3 comprises a ligand for an E3 ligase, a photoswitch, and the BET bromodomain targeting ligand (+)-JQ1. Exhibits cytotoxicity and degrades BRD4, BRD3 and to a lesser extent BRD2 in lymphoblast cells upon irradiation with 390 nm light, but not in the dark.
T18820 Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride

Others Others
Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride is a chemical compound that has been synthesized as an E3 ligase ligand-linker conjugate. This compound incorporates a cereblon ligand derived from Thalidomide and a 3-unit PEG linker. It is specifically designed for use in PROTAC technology, which utilizes small molecules to induce protein degradation [1].
T18068 Lenalidomide-PEG3-iodine

Others Others
Lenalidomide-PEG3-iodine, an E3 ligase ligand-linker conjugate, consists of a cereblon-based Lenalidomide ligand and a 3-unit polyethylene glycol (PEG) linker. This compound is utilized in creating various proteolysis targeting chimeras (PROTACs), including the highly effective PROTAC BTK degrader SJF620, which has a degradation concentration 50 (DC50) of 7.9 nM[1].
T39806 Pomalidomide 4'-PEG3-azide

Pomalidomide 4'-PEG3-azide

Pomalidomide 4'-PEG3-azide is a chemically synthesized conjugate consisting of an E3 ligase ligand-linker conjugate that incorporates the cereblon ligand derived from Pomalidomide, along with a linker. This compound, Pomalidomide 4'-PEG3-azide, is utilized in the synthesis of iRucaparib-TP3 (Compound 3). iRucaparib-TP3, developed through the PROTAC strategy, is an effective degrader of PARP1, derived from Rucaparib.

化合物

E3 ligase Ligand 8
Cat.No: T17879
Synonym:
Target: Others, Ligand for E3 Ligase
E3 ligase Ligand 23
Cat.No: T9809
Synonym:
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
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 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
(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
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
(S,R,S)-AHPC-PEG2-NH2 hydrochloride
Cat.No: T17924
Synonym: VH032-PEG2-NH2 hydrochloride,VHL Ligand-Linker Conjugates 3 hydrochloride,E3 ligase Ligand-Linker Conjugates 6
Target: Others, E3 Ligase Ligand-Linker Conjugate
(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
(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
Pomalidomide-C3-NH2 hydrochloride
Cat.No: T40002
Synonym:
Target: Others, E3 Ligase Ligand-Linker Conjugate
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
E3 ligase Ligand 13
Cat.No: T17871
Synonym:
Target: Others
E3 ligase Ligand 10
Cat.No: T17868
Synonym:
Target: Others
E3 ligase Ligand 9
Cat.No: T17880
Synonym:
Target: Others
E3 ligase Ligand 18
Cat.No: T17876
Synonym:
Target: Others
E3 ligase Ligand 14
Cat.No: T17872
Synonym:
Target: Others
cIAP1 Ligand-Linker Conjugates 3
Cat.No: T17894
Synonym: E3 ligase Ligand-Linker Conjugates 40
Target: Others
Thalidomide-NH-PEG1-NH2 hydrochloride
Cat.No: T9401
Synonym: 4-[(2-(2-Aminoethoxy)ethyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione HCl
Target: E3 Ligase Ligand-Linker Conjugate
Thalidomide-O-amido-PEG3-C2-NH2
Cat.No: T17915
Synonym: Cereblon Ligand-Linker Conjugates 3,E3 Ligase Ligand-Linker Conjugates 14
Target: Others
(S,R,S)-AHPC-PEG2-NH2
Cat.No: T17925
Synonym: VH032-PEG2-NH2,VHL Ligand-Linker Conjugates 3,E3 ligase Ligand-Linker Conjugates 6 Free Base
Target: Others, E3 Ligase Ligand-Linker Conjugate
Pomalidomide-PEG3-C2-NH2
Cat.No: T17883
Synonym: Cereblon Ligand-Linker Conjugates 5,E3 ligase Ligand-Linker Conjugates 30
Target: Others, PROTAC Linker
Thalidomide-O-amido-C3-COOH
Cat.No: T17914
Synonym: Cereblon Ligand-Linker Conjugates 7,E3 ligase Ligand-Linker Conjugates 15
Target: Others
Pomalidomide-amido-PEG3-C2-NH2
Cat.No: T18553
Synonym: Cereblon Ligand-Linker Conjugates 22,E3 ligase Ligand-Linker Conjugates 55
Target: Others
Thalidomide-NH-C2-PEG3-OH
Cat.No: T9382
Synonym: H-Isoindole-1,3(2H)-dione, 2-(2,6-dioxo-3-piperidinyl)-4-[[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl]amino]-
Target: E3 Ligase Ligand-Linker Conjugate
(S,R,S)-AHPC-PEG3-NH2
Cat.No: T17923
Synonym: E3 ligase Ligand-Linker Conjugates 5 Free Base,VH032-PEG3-NH2,VHL Ligand-Linker Conjugates 1
Target: Others
Thalidomide-O-C6-NH2 hydrochloride
Cat.No: T40031
Synonym: 4-((6-aminohexyl)oxy)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride,萨力多胺-O-C6-氨基盐酸盐
Target: E3 Ligase Ligand-Linker Conjugate
(S,R,S)-AHPC-(C3-​PEG)​2-​C6-​Cl
Cat.No: T17912
Synonym: VHL Ligand-Linker Conjugates 11,E3 ligase Ligand-Linker Conjugates 11
Target: Others
Pomalidomide-PEG3-C2-NH2 (TFA)
Cat.No: T17882
Synonym: Cereblon Ligand-Linker Conjugates 5 (TFA),E3 ligase Ligand-Linker Conjugates 30 (TFA),Pomalidomide-PEG3-C2-NH2 (TFA) (2093416-31-8 free base)
Target: Others
Pomalidomide-C2-NH2
Cat.No: T17875
Synonym: Cereblon Ligand-Linker Conjugates 15,4-[(2-Aminoethyl)amino]-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione
Target: Others, Ligand for E3 Ligase
Pomalidomide-PEG3-CO2H
Cat.No: T40023
Synonym: Thalidomide-NH-PEG3-propionic acid
Target: E3 Ligase Ligand-Linker Conjugate
Thalidomide-NH-CH2-COOH
Cat.No: T40016
Synonym: 2-[[2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindol-4-yl]amino]acetic acid,(2-(2,6-Dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)glycine
Target: Ligand for E3 Ligase
Pomalidomide-PEG3-azide
Cat.No: T39804
Synonym: Pomalidomide-PEG3-azide
Target:
PROTAC MDM2 Degrader-3
Cat.No: T18633
Synonym:
Target: Others
(S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH
Cat.No: T39494
Synonym: VH032-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH,(S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH
Target:
Thalidomide-O-amido-C3-PEG3-C1-NH2
Cat.No: T39215
Synonym: Thalidomide-O-amido-C3-PEG3-C1-NH2
Target:
Thalidomide-O-amido-PEG1-(C1-​PEG)2-C2-NH2
Cat.No: T17917
Synonym: E3 Ligase Ligand-Linker Conjugates 23 TFA,Cereblon Ligand-Linker Conjugates 12 TFA
Target: Others
Nutlin-C1-amido-PEG4-C2-N3
Cat.No: T17902
Synonym: E3 ligase Ligand-Linker Conjugates 48,MDM2 Ligand-Linker Conjugates 1
Target: Others
BRD PHOTAC-I-3
Cat.No: T41198
Synonym:
Target:
Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride
Cat.No: T18820
Synonym:
Target: Others
Lenalidomide-PEG3-iodine
Cat.No: T18068
Synonym:
Target: Others
Pomalidomide 4'-PEG3-azide
Cat.No: T39806
Synonym: Pomalidomide 4'-PEG3-azide
Target:
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