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173

抑制剂 & 化合物

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Cat. No. Product Name Target Signaling Pathways
T0213 Thalidomide

Thalomid,沙利度胺,Sedoval

Apoptosis; TNF; Autophagy; Ligand for E3 Ligase; Molecular Glues Apoptosis; Autophagy; PROTAC
Thalidomide (Thalomid) 能够抑制 cereblon,即 cullin-4 E3 泛素连接酶复合物 CUL4-RBX1-DDB1 的一部分,Kd 值约为 250 nM,具有免疫调节、抗炎、抗肿瘤作用。它可以作为分子胶来增强底物。
T12644L (S)-Thalidomide

(S)-(-)-Thalidomide

Apoptosis Apoptosis
(S)-Thalidomide ((S)-(-)-Thalidomide) 是 Thalidomide 的 S 型异构体,具有免疫调节,抗炎,抗癌,抗血管生成活性和促凋亡活性,可用于研究麻风结节性红斑和骨髓瘤。
T9389 Thalidomide-PEG4-Propargyl

Thalidomide-O-PEG4-Propargyl

E3 Ligase Ligand-Linker Conjugate PROTAC
Thalidomide-PEG4-Propargyl (Thalidomide-O-PEG4-Propargyl) 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,。
T18831 Thalidomide-propargyl

Others; Ligand for E3 Ligase Others; PROTAC
Thalidomide-propargyl 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,得到含 IMiD 的 PROTAC。
T40503 Thalidomide-5-methyl

Ligand for E3 Ligase PROTAC
Thalidomide-5-methyl 是基于 Thalidomide 的 CRBN 配体,可以用于CRBN 的招募。
T40011 Thalidomide-CH2CONH-C3-COOH

Others Others
Thalidomide-CH2CONH-C3-COOH 是一种合成的 E3 连接酶配体-接头偶联物,它结合了 PROTAC 技术中使用的基于Thalidomide 的CRBN 配体和接头。
T40013 Thalidomide-O-CH2CONH-CH2COOH

Others Others
Thalidomide-O-CH2CONH-CH2COOH 是一种合成的 E3 连接酶配体-接头偶联物,它结合了 PROTAC 技术中使用的基于 Thalidomide 的 CRBN 配体和接头。
T40012 Thalidomide-CH2CONH-C2-COOH

Others Others
Thalidomide-CH2CONH-C2-COOH 是一种合成的 E3 连接酶配体-接头偶联物,它结合了 PROTAC 技术中使用的基于Thalidomide 的CRBN 配体和接头。
T9402 Thalidomide-O-C4-NH2 hydrochloride

E3 Ligase Ligand-Linker Conjugate PROTAC
Thalidomide-O-C4-NH2 hydrochloride 包含基于 Thalidomide 的 cereblon 配体和 PROTAC 技术中使用的接头,是一种合成的 E3 连接酶配体-接头偶联物。
T18807 Thalidomide-NH-C4-NH-Boc

E3 Ligase Ligand-Linker Conjugate; Ligand for E3 Ligase PROTAC
Thalidomide-NH-C4-NH-Boc 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。
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。
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。
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。
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。
T9291 Thalidomide-5-OH

4 - 羟基沙利度胺,2-(2,6-dioxopiperidin-3-yl)-5-hydroxyisoindoline-1,3-dione

Others; Ligand for E3 Ligase Others; PROTAC
Thalidomide-5-OH (2-(2,6-dioxopiperidin-3-yl)-5-hydroxyisoindoline-1,3-dione) 是基于 Thalidomide 的的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。
T40003 Thalidomide-NH-C6-NH2 hydrochloride

Others; E3 Ligase Ligand-Linker Conjugate Others; PROTAC
Thalidomide-NH-C6-NH2 hydrochloride 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。
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。
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。
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。
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。
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。
T40030 Thalidomide 4'-ether-alkylC2-amine hydrochloride

halidomide-linker 6

E3 Ligase Ligand-Linker Conjugate PROTAC
Thalidomide 4'-ether-alkylC2-amine hydrochloride (halidomide-linker 6) 包含基于 Thalidomide 的 cereblon 配体和 linker,是合成的 E3 连接酶配体-linker 偶联物,可应用于 PROTAC 技术。
T12644 (R)-Thalidomide

(R)-(+)-Thalidomide

Others Others
(R)-Thalidomide is the R-enantiomer of Thalidomide, has sedative properties.
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,。
T18818 Thalidomide-O-amido-PEG-C2-NH2 hydrochloride

Others; E3 Ligase Ligand-Linker Conjugate Others; PROTAC
Thalidomide-O-amido-PEG-C2-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 的合成分子。
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。
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。
T39925 Thalidomide-NH-PEG3-COOH

Thalidomide-NH-PEG3-COOH

Thalidomide-NH-PEG3-COOH is a conjugate of the E3 ligase ligand-linker synthesized compound, which integrates a cereblon ligand based on Thalidomide and a linker employed in PROTAC technology.
T39496 Thalidomide-O-C5-acid

Thalidomide-O-C5-acid

Thalidomide-O-C5-acid is a chemically synthesized conjugate that acts as an E3 ligase ligand-linker and combines the cereblon ligand derived from Thalidomide with a linker commonly utilized in PROTAC technology.
T40149 Thalidomide-NH-PEG8-Ts

Thalidomide-NH-PEG8-Ts

Thalidomide-NH-PEG8-Ts is a chemically synthesized conjugate consisting of a Thalidomide-based cereblon ligand and an 8-unit PEG linker. This conjugate serves as an E3 ligase ligand-linker in PROTAC technology applications, including the degradation of IDO1 by a PROTAC degrader.
T39644 Thalidomide-O-C6-COOH

Thalidomide-O-C6-COOH

Thalidomide-O-C6-COOH is a synthetic conjugate comprising an E3 ligase ligand-linker, which combines the Thalidomide derived cereblon ligand with a PROTAC technology linker.
T39642 Thalidomide-O-C3-acid

Thalidomide-O-C3-acid

Thalidomide-O-C3-acid is a chemically derived conjugate that combines a cereblon ligand based on Thalidomide and a linker commonly employed in PROTAC technology. This synthesized E3 ligase ligand-linker conjugate serves to facilitate targeted protein degradation.
T39645 Thalidomide-O-C7-acid

Thalidomide-O-C7-acid

Thalidomide-O-C7-acid is a compound created through the synthesis of an E3 ligase ligand-linker conjugate. It consists of a cereblon ligand derived from Thalidomide, combined with a linker that is commonly employed in PROTAC technology.
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。
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。
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。
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。
T39382 Thalidomide-NH-C8-NH2

Thalidomide-NH-C8-NH2

Thalidomide-NH-C8-NH2 is a synthetic conjugate of an E3 ligase ligand-linker, which combines a cereblon ligand based on Thalidomide with a specific linker utilized in PROTAC technology.
T39376 Thalidomide-O-C8-NH2

Thalidomide-O-C8-NH2

Thalidomide-O-C8-NH2 is a chemically synthesized conjugate that combines a cereblon ligand derived from Thalidomide with a linker utilized in PROTAC technology. It functions as an E3 ligase ligand-linker conjugate.
T40036 Thalidomide-NH-PEG4-COOH

Thalidomide-NH-PEG4-COOH

Thalidomide-NH-PEG4-COOH is a conjugate comprising an E3 ligase ligand-linker, utilized in the synthesis of dCBP-1. dCBP-1 itself functions as a powerful and selective heterobifunctional degrader targeting p300/CBP.
T39377 Thalidomide-PEG2-NH2

Thalidomide-PEG2-NH2

Thalidomide-PEG2-NH2 is a chemically synthesized E3 ligase ligand-linker conjugate consisting of a ligand derived from Thalidomide-based cereblon and a linker commonly employed in PROTAC technology.
T39379 Thalidomide-PEG3-NH2

Thalidomide-PEG3-NH2

Thalidomide-PEG3-NH2 is a synthesized conjugate comprising an E3 ligase ligand-linker conjugate that integrates a cereblon ligand based on Thalidomide and a linker employed in PROTAC technology.
T39604 Thalidomide-NH-PEG4-Ms

Thalidomide-NH-PEG4-Ms

Thalidomide-NH-PEG4-Ms is a conjugate that consists of a cereblon ligand based on Thalidomide and a linker molecule, which serves as a ligand-linker moiety for E3 ligase. This conjugate is specifically designed as a degrader for PROTAC BCL-XL, known as XZ739.
T39893 Thalidomide-Piperazine-PEG2-NH2

Thalidomide-Piperazine-PEG2-NH2

Thalidomide-Piperazine-PEG2-NH2 is a synthetic E3 ligase ligand-linker conjugate that combines the cereblon ligand derived from Thalidomide with a linker commonly utilized in PROTAC technology.
T39950 Thalidomide-amido-PEG2-NH2

Thalidomide-amido-PEG2-NH2

Thalidomide-amido-PEG2-NH2 is a synthetic conjugate of an E3 ligase ligand-linker that combines the Thalidomide-based cereblon ligand with a linker commonly utilized in PROTAC technology.
T39511 Thalidomide-O-C7-NH2

Thalidomide-O-C7-NH2

Thalidomide-O-C7-NH2 is a synthesized conjugate compound comprising an E3 ligase ligand-linker conjugate. This compound incorporates a cereblon ligand based on Thalidomide and a linker that is commonly employed in PROTAC technology.
T39964 Thalidomide-PEG4-NH2 hydrochloride

Thalidomide-PEG4-NH2 hydrochloride

Thalidomide-PEG4-NH2 hydrochloride is a compound synthesized as an E3 ligase ligand-linker conjugate. It encompasses the cereblon ligand derived from Thalidomide and a linker utilized specifically in PROTAC technology.
T39917 Thalidomide-O-C2-acid

Thalidomide-O-C2-acid

Thalidomide-O-C2-acid is a compound designed by synthesizing an E3 ligase ligand-linker conjugate. It comprises a cereblon ligand derived from Thalidomide and a linker commonly used in PROTAC technology.
T39643 Thalidomide-O-C4-COOH

Thalidomide-O-C4-COOH

Thalidomide-O-C4-COOH is a synthetic conjugate compound, serving as an E3 ligase ligand-linker, which combines a cereblon ligand derived from Thalidomide and a linker utilized in PROTAC technology.
T39721 Thalidomide-5-PEG2-Cl

Thalidomide-5-PEG2-Cl

Thalidomide-5-PEG2-Cl, a Thalidomide-derived cereblon ligand, serves as the ligand for the recruitment of CRBN protein. It can be conjugated to the protein ligand via a linker to produce PROTACs.

化合物

Thalidomide
Cat.No: T0213
Synonym: Thalomid,沙利度胺,Sedoval
Target: Apoptosis, TNF, Autophagy, Ligand for E3 Ligase, Molecular Glues
(S)-Thalidomide
Cat.No: T12644L
Synonym: (S)-(-)-Thalidomide
Target: Apoptosis
Thalidomide-PEG4-Propargyl
Cat.No: T9389
Synonym: Thalidomide-O-PEG4-Propargyl
Target: E3 Ligase Ligand-Linker Conjugate
Thalidomide-propargyl
Cat.No: T18831
Synonym:
Target: Others, Ligand for E3 Ligase
Thalidomide-5-methyl
Cat.No: T40503
Synonym:
Target: Ligand for E3 Ligase
Thalidomide-CH2CONH-C3-COOH
Cat.No: T40011
Synonym:
Target: Others
Thalidomide-O-CH2CONH-CH2COOH
Cat.No: T40013
Synonym:
Target: Others
Thalidomide-CH2CONH-C2-COOH
Cat.No: T40012
Synonym:
Target: Others
Thalidomide-O-C4-NH2 hydrochloride
Cat.No: T9402
Synonym:
Target: E3 Ligase Ligand-Linker Conjugate
Thalidomide-NH-C4-NH-Boc
Cat.No: T18807
Synonym:
Target: 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
Thalidomide-4-OH
Cat.No: T7763
Synonym: Cereblon ligand 2,E3 ligase Ligand 2
Target: 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
Thalidomide-O-COOH
Cat.No: T7753
Synonym: Cereblon ligand 3,E3 ligase Ligand 3,TCE35031
Target: Others, Ligand for E3 Ligase
Thalidomide-5-OH
Cat.No: T9291
Synonym: 4 - 羟基沙利度胺,2-(2,6-dioxopiperidin-3-yl)-5-hydroxyisoindoline-1,3-dione
Target: Others, Ligand for E3 Ligase
Thalidomide-NH-C6-NH2 hydrochloride
Cat.No: T40003
Synonym:
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-PEG2-C2-NH2 hydrochloride
Cat.No: T18819
Synonym:
Target: Others, Ligand for E3 Ligase
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
Thalidomide-5-NH2-CH2-COOH
Cat.No: T40019
Synonym:
Target: Others
Thalidomide-O-amido-C6-NH2 hydrochloride
Cat.No: T18816
Synonym:
Target: Others, E3 Ligase Ligand-Linker Conjugate
Thalidomide 4'-ether-alkylC2-amine hydrochloride
Cat.No: T40030
Synonym: halidomide-linker 6
Target: E3 Ligase Ligand-Linker Conjugate
(R)-Thalidomide
Cat.No: T12644
Synonym: (R)-(+)-Thalidomide
Target: Others
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-PEG-C2-NH2 hydrochloride
Cat.No: T18818
Synonym:
Target: Others, E3 Ligase Ligand-Linker Conjugate
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
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-NH-PEG3-COOH
Cat.No: T39925
Synonym: Thalidomide-NH-PEG3-COOH
Target:
Thalidomide-O-C5-acid
Cat.No: T39496
Synonym: Thalidomide-O-C5-acid
Target:
Thalidomide-NH-PEG8-Ts
Cat.No: T40149
Synonym: Thalidomide-NH-PEG8-Ts
Target:
Thalidomide-O-C6-COOH
Cat.No: T39644
Synonym: Thalidomide-O-C6-COOH
Target:
Thalidomide-O-C3-acid
Cat.No: T39642
Synonym: Thalidomide-O-C3-acid
Target:
Thalidomide-O-C7-acid
Cat.No: T39645
Synonym: Thalidomide-O-C7-acid
Target:
Tz-Thalidomide
Cat.No: T77912
Synonym:
Target: Epigenetic Reader Domain
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
Pomalidomide-PEG3-CO2H
Cat.No: T40023
Synonym: Thalidomide-NH-PEG3-propionic acid
Target: E3 Ligase Ligand-Linker Conjugate
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
Thalidomide-NH-C8-NH2
Cat.No: T39382
Synonym: Thalidomide-NH-C8-NH2
Target:
Thalidomide-O-C8-NH2
Cat.No: T39376
Synonym: Thalidomide-O-C8-NH2
Target:
Thalidomide-NH-PEG4-COOH
Cat.No: T40036
Synonym: Thalidomide-NH-PEG4-COOH
Target:
Thalidomide-PEG2-NH2
Cat.No: T39377
Synonym: Thalidomide-PEG2-NH2
Target:
Thalidomide-PEG3-NH2
Cat.No: T39379
Synonym: Thalidomide-PEG3-NH2
Target:
Thalidomide-NH-PEG4-Ms
Cat.No: T39604
Synonym: Thalidomide-NH-PEG4-Ms
Target:
Thalidomide-Piperazine-PEG2-NH2
Cat.No: T39893
Synonym: Thalidomide-Piperazine-PEG2-NH2
Target:
Thalidomide-amido-PEG2-NH2
Cat.No: T39950
Synonym: Thalidomide-amido-PEG2-NH2
Target:
Thalidomide-O-C7-NH2
Cat.No: T39511
Synonym: Thalidomide-O-C7-NH2
Target:
Thalidomide-PEG4-NH2 hydrochloride
Cat.No: T39964
Synonym: Thalidomide-PEG4-NH2 hydrochloride
Target:
Thalidomide-O-C2-acid
Cat.No: T39917
Synonym: Thalidomide-O-C2-acid
Target:
Thalidomide-O-C4-COOH
Cat.No: T39643
Synonym: Thalidomide-O-C4-COOH
Target:
Thalidomide-5-PEG2-Cl
Cat.No: T39721
Synonym: Thalidomide-5-PEG2-Cl
Target:
Cat. No. Product Name Target Signaling Pathways
TN3098 5-hydroxythalidomide

5,8,9,14-Tetraacetoxy-3-benzoyloxy-10,15-dihydroxypepluane

Others Others
5-hydroxythalidomide 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3098,CAS号为 219916-77-5。

天然产物

5-hydroxythalidomide
Cat.No: TN3098
Synonym: 5,8,9,14-Tetraacetoxy-3-benzoyloxy-10,15-dihydroxypepluane
Target: Others
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