关于 "Aldehyde Dehydrogenase (ALDH)" 的结果45+ 个结果
- (+)-JQ-1-aldehyde
(+)-JQ-1-aldehyde是(+)-JQ1的醛形式。(+)-JQ-1-aldehyde可作为合成PROTACs的前体,靶向BET溴结构域.。
- Aldehyde-benzyl-PEG5-alkyneCAS: 1378928-83-6
Aldehyde-benzyl-PEG5-alkyne 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。
- TBS-Corey Lactone AldehydeCAS: 64091-14-1
An intermediate for the synthesis of prostaglandins and their analogs
- Aldehyde Reactive Probe (trifluoroacetate salt)CAS: 627090-10-2
A biotinylated probe for detecting AP sites in damaged DNA
- 1-Naphthalenylsulfonyl-Ile-Trp-aldehydeCAS: 161709-56-4
Cell-permeable and reversible inhibitor of cathepsin L, a lysosomal cysteine protease ( IC?? 1.9 nM). 1-Naphthalenylsulfonyl-IW-CHO inhibited the release of Ca²? and hydroxyproline from bone in an in vitro bone culture system. It should be useful for the treatment of osteoporosis.
- Ac-Leu-Val-Lys-aldehydeCAS: 147600-40-6
Ac-LVK-CHO, the lysinal analog of leupeptin showed a stronger inhibition of cathepsin B (IC?? = 4 nM) than leupeptin (IC?? = 0.31 µM).
- Ac-Leu-Val-Phe-aldehydeCAS: 160369-84-6
Ac-LVF-CHO has been shown to act as a potent HIV protease inhibitor (IC??= 0.9 µM) and to have increased activity against cathepsin D and pepsin (IC??= 37 µM and 100 µM).
- Z-Pro-Pro-aldehyde-dimethyl acetalCAS: 170116-63-9
Z-PP-CHO dimethylacetal was shown to be a potent inhibitor of prolyl endopeptidase (PEP), a cytoplasmic serine endoprotease (IC??= 120 nM). It is suggested that PEP inhibitors could be useful for the treatment of cognitive dysfunction in aging and neurodegenerative diseases including Alzheimer's disease.
- H-Gly-Phe-Gly-aldehyde semicarbazoneCAS: 102579-48-6
The reversible cathepsin B inhibitor GFG-aldehyde semicarbazone has been used in the purification of the cathepsin B-like proteinase Sj31 from Schistosoma japonicum by affinity chromatography and for isolating falcipains from Plasmodium species.
| 货号 | 产品名称 | CAS号 | 靶点 / 通路 | 引用 | 结构 |
|---|---|---|---|---|---|
| GC78622 | (+)-Abscisic aldehyde | 41944-86-9 | - | ||
(+)-Abscisic Aldehyde (ABAld) 是一种植物激素脱落酸 (ABA) 生物合成的中间产物。 | |||||
| GA21501 | Fmoc-Ala-aldehyde | 146803-41-0 | - | ||
Fmoc-L-alaninal. | |||||
| GA20885 | Boc-Ala-aldehyde | 79069-50-4 | - | ||
Boc-L-alaninal. | |||||
| GC61595 | (+)-JQ-1-aldehyde | - | Epigenetic Reader Domain | ||
(+)-JQ-1-aldehyde是(+)-JQ1的醛形式。(+)-JQ-1-aldehyde可作为合成PROTACs的前体,靶向BET溴结构域.。 | |||||
| GC66831 | Aldehyde-benzyl-PEG5-alkyne | 1378928-83-6 | PROTAC Linker | ||
Aldehyde-benzyl-PEG5-alkyne 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。 | |||||
| GC15896 | Z-Ile-Leu-aldehyde | 161710-10-7 | Gamma Secretase | ||
Z-Ile-Leu-aldehyde (Z-IL-CHO) 是一种有效的、竞争性的 γ-分泌酶和缺口肽醛抑制剂。 | |||||
| GC66501 | Azido-PEG3-aldehyde | 1807530-10-4 | PROTAC Linker | ||
Azido-PEG3-aldehyde 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。 | |||||
| GC66597 | m-PEG4-aldehyde | 197513-96-5 | PROTAC Linker | ||
m-PEG4-aldehyde 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。 | |||||
| GA21153 | Boc-Tyr(Bzl)-aldehyde | 82689-15-4 | - | ||
Protected Boc-tyrosinal derivative. | |||||
| GA21578 | Fmoc-D-Ala-aldehyde | 127043-32-7 | - | ||
Fmoc-D-alaninal. | |||||
| GC41372 | Corey Lactone Aldehyde Benzoate | 39746-01-5 | Cyclooxygenase | ||
Chiral intermediate used to produce prostaglandins | |||||
| GC45002 | TBS-Corey Lactone Aldehyde | 64091-14-1 | Cyclooxygenase | ||
An intermediate for the synthesis of prostaglandins and their analogs | |||||
| GC42765 | Aldehyde Reactive Probe (trifluoroacetate salt) | 627090-10-2 | DNA/RNA Oxidative Damage | ||
A biotinylated probe for detecting AP sites in damaged DNA | |||||
| GC66613 | m-PEG4-CH2-aldehyde | 1059189-65-9 | PROTAC Linker | ||
m-PEG4-CH2-aldehyde 是一种基于 PEG 的 PROTAC linker,用于 PROTAC 合成。 | |||||
| GA20375 | 1-Naphthalenylsulfonyl-Ile-Trp-aldehyde | 161709-56-4 | - | ||
Cell-permeable and reversible inhibitor of cathepsin L, a lysosomal cysteine protease ( IC?? 1.9 nM).
1-Naphthalenylsulfonyl-IW-CHO inhibited the release of Ca²? and hydroxyproline from bone in an in vitro bone culture system. It should be useful for the treatment of osteoporosis. | |||||
| GA20598 | Ac-Leu-Val-Lys-aldehyde | 147600-40-6 | - | ||
Ac-LVK-CHO, the lysinal analog of leupeptin showed a stronger inhibition of cathepsin B (IC?? = 4 nM) than leupeptin (IC?? = 0.31 µM). | |||||
| GA20599 | Ac-Leu-Val-Phe-aldehyde | 160369-84-6 | - | ||
Ac-LVF-CHO has been shown to act as a potent HIV protease inhibitor (IC??= 0.9 µM) and to have increased activity against cathepsin D and pepsin (IC??= 37 µM and 100 µM). | |||||
| GA20904 | Boc-Asn-Phe-Pro-aldehyde | 249757-11-7 | - | ||
Boc-NFP-aldehyde inhibits prolyl endopeptidases. | |||||
| GC30214 | Pyruvic aldehyde (~40% in water) | 78-98-8 | Endogenous Metabolite | ||
Pyruvicaldehyde常被用作有机合成中的一种试剂,一种调味剂以及在鞣革中的应用。 | |||||
| GA23930 | Z-Pro-Pro-aldehyde-dimethyl acetal | 170116-63-9 | - | ||
Z-PP-CHO dimethylacetal was shown to be a potent inhibitor of prolyl endopeptidase (PEP), a cytoplasmic serine endoprotease (IC??= 120 nM). It is suggested that PEP inhibitors could be useful for the treatment of cognitive dysfunction in aging and neurodegenerative diseases including Alzheimer's disease. | |||||
| GA22490 | H-Gly-Phe-Gly-aldehyde semicarbazone | 102579-48-6 | - | ||
The reversible cathepsin B inhibitor GFG-aldehyde semicarbazone has been used in the purification of the cathepsin B-like proteinase Sj31 from Schistosoma japonicum by affinity chromatography and for isolating falcipains from Plasmodium species. | |||||
