16
6
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T41090 |
L-Azidohomoalanine hydrochloride
H-L-Aha-OH hydrochloride |
PROTAC Linker | PROTAC |
L-Azidohomoalanine hydrochloride (H-L-Aha-OH hydrochloride) 是一种基于烷基链的 PROTAC 接头。 | |||
T1592 |
Acetohydroxamic acid
Methylhydroxamic acid,Acetic acid,Lithostat,AHA,oxime,N-Hydroxyacetamide,乙酰氧肟酸 |
MMP; Antibacterial | Microbiology/Virology; Proteases/Proteasome |
Acetohydroxamic acid (N-Hydroxyacetamide) 是一种不可逆的细菌和植物尿素酶抑制剂,可研究慢性尿路感染。 | |||
T62307 | Aha1/Hsp90-IN-1 | ||
Aha1/Hsp90-IN-1 (Compound 17) 是一种 Aha1/Hsp90 complex 抑制剂,对 tau 蛋白聚集具有抑制作用。Aha1/Hsp90-IN-1 能够破坏 Aha1/Hsp90 的相互作用 (IC50: 3.32 μM)。 | |||
T19556 |
SAHA chloroalkane T1
|
Others | Others |
SAHA chloroalkane T1 is a novel compound formed by combining Vorinostat (SAHA) with a chloroalkane capture tag, referred to as T1. This innovative approach involves tethering the SAHA molecule with the T1 tag, resulting in the formation of SAHA chloroalkane T1. | |||
T25565 | Kahalalide A | ||
Kahalalide A has antimycobacterial activity isolated from the mollusk Elysia rufescens. | |||
T71011 | Perfluorinated SAHA | ||
Perfluorinated SAHA is an HDAC inhibitor for use in cancer treatment regimens, with demonstrated greater antiproliferative properties than SAHA . PFSAHA has also been shown to have higher selectivity for PA3774, an HDAC-like enzyme from P. aeruginosa, as well as other HDACs, which may prove beneficial for developing novel chemotherapeutic treatments for cancer. | |||
T27804 | LCAHA | ||
LCAHA is a USP2a inhibitor. LCAHA inhibits growth of cyclin D1-dependent cells. | |||
T36105 |
coumarin-SAHA
coumarin-Suberoylanilide Hydroxamic Acid,coumarin-SAHA |
||
Suberoylanilide hydroxamic acid (SAHA) is a class I and class II histone deacetylase (HDAC) inhibitor that binds directly to the catalytic site of the enzyme thereby blocking substrate access. [1] coumarin-Suberoylanilide hydroxamic acid (c-SAHA) is a SAHA derivative where the anilino cap" group is replaced by 7-amino-4-methylcoumarin to produce a fluorescent probe that competitively binds HDAC. [2] The fluorescence excitation and emission maxima of free c-SAHA is 325 and 400 nm | |||
T125152 |
Isomahanimbine
|
||
Isomahanimbine 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T125152。 | |||
T21749 |
4-iodo-SAHA
|
||
4-Iodo-SAHA (1k) 是一种具有口服活性的I 类和II 类histone deacetylase (HDAC)抑制剂,对 Skbr3、 HT29、 U937、 JA16 和 HL60细胞的EC50值分别为1.1、0.95、0.12、0.24、0.85和1.3 μM。4-Iodo-SAHA (1k) 可用于癌症的研究。 | |||
T25342 | Discobahamin A | ||
Discobahamin A is a bioactive peptide isolated from a new species of the Bahamian deep water marine sponge Discodermia. It is a growth of Candida albicans inhibitor. | |||
T125848 | Isomahanine | ||
Isomahanine 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T125848。 | |||
T25343 | Discobahamin B | ||
Discobahamin B is a bioactive peptide isolated from a new species of the Bahamian deep water marine sponge Discodermia. It is a growth of Candida albicans inhibitor. | |||
T73454 | SAHA-OH | HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
SAHA-OH为HDAC6选择性抑制剂(IC50=23 nM),对HDAC6具有10至47倍选择性,相较于HDAC1、2、3及8。该化合物展现抗炎活性,能够降低巨噬细胞凋亡。 | |||
T35765 |
SAHA-BPyne
|
||
Suberoylanilide hydroxamic acid (SAHA) is a class I and class II histone deacetylase (HDAC) inhibitor that binds directly to the catalytic site of the enzyme thereby blocking substrate access. SAHA-BPyne is a SAHA derivative with a benzophenone crosslinker and an alkyne tag intended to be used for profiling HDAC activities in proteomes and live cells. Such terminal alkyne groups can be used in linking reactions, known as click chemistry, characterized by high dependability and specificity of azi... | |||
T80422 |
Phoenixin-14
PNX-14 |
GNRH Receptor | GPCR/G Protein |
Phoenixin-14 (PNX-14) 是一种具有内源性活性的异构体,能通过激活AHA GnRH系统发挥抗焦虑效果,并抑制缺血/再灌注所诱导的小胶质细胞毒性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN5082 |
Swietemahalactone
|
Antifection | Microbiology/Virology |
Swietemahalactone exhibits antibacterial activity. | |||
TN6198 |
Mahanine
|
||
Mahanine has effects on the activation of the apoptotic pathway in human leukemia U937 cells, causes the mitochondrial membranes to lose their permeability, resulting in caspase-3 activation and apoptosis. Mahanine can reverse an epigenetically silenced g | |||
TN6099 |
Mahanimbilol
Mahanimbinol |
||
Mahanimbilol 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 TN6099,CAS号为 77156-13-9。 | |||
T81877 | Mahanimbidine | ||
Mahanimbidine为一种萜类生物碱,可从Murraya koenigii Spreng的叶与茎皮中提取分离。 | |||
T15949 |
Mahanimbine
|
AChE | Neuroscience |
Mahanimbine 存在于Murraya koenigii 的根、叶和茎中,是从Murraya koenigii 中的提取的一种具有口服活性的生物碱。Mahanimbine 具有乙酰胆碱酯酶抑制活性,可抑制了高脂肪饮食(HFD)引起的小鼠代谢并发症的发展,对科尼氏分枝杆菌叶对链脲佐菌素诱导的糖尿病大鼠胰腺β细胞组织病理学变化有作用。 | |||
TN4933 |
Sahandol
|
Antifection | Microbiology/Virology |
Sahandol shows antiprotozoal activity against P. falciparum and T. brucei rhodesiense. |