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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T21505 | Suberoyl bis-hydroxamic acid | SBHA,Suberohydroxamic acid | Apoptosis , HDAC |
Suberoyl bis-hydroxamic acid (SBHA) is a Histone deacetylase (HDAC) inhibitor. HDAC is required for transcriptional modulation, cell cycle regulation and development. It is an enzyme that deacetylates lysine residues on ... | |||
T1583 | Vorinostat | MK0683,suberoylanilide hydroxamic acid,SAHA | Apoptosis , Mitophagy , Virus Protease , HDAC , Autophagy |
Vorinostat (SAHA) is a pan-histone deacetylase (HDAC) inhibitor (IC50=10 nM) with inhibitory activity against HDAC1/2/3/6/7/11. Vorinostat has antitumor activity, induces cell differentiation, blocks the cell cycle and i... | |||
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-Suberoylanili... | |||
T14864 | Caracemide | NSC-253272 | Others , DNA/RNA Synthesis , Antibacterial |
Caracemide (NSC-253272) inhibits the enzyme ribonucleotide reductase of Escherichia coli. Caracemide can be used in anticancer studies. | |||
T13996 | 1-Naphthohydroxamic acid | HDAC | |
1-Naphthohydroxamic acid (Compound 2) is a potent and selective HDAC8 inhibitor with an IC50 of 14 μM, and it is more selectively for HDAC8 than class I HDAC1 and class II HDAC6 (IC50 >100 μM). 1-Naphthohydroxamic acid d... | |||
T1592 | Acetohydroxamic acid | Methylhydroxamic acid,Acetic acid,Lithostat,AHA,oxime,N-Hydroxyacetamide | MMP , Antibacterial |
Acetohydroxamic acid (N-Hydroxyacetamide) is an antagonist of the bacterial enzyme urease. | |||
T72148 | Phosphoglycolohydroxamic acid | ||
Phosphoglycolohydroxamic acid, acting as a potent inhibitor of both aldolase and triose-phosphate isomerase, serves a crucial role in the research of antibacterial and antifungal domains. | |||
T33614 | N-Decanohydroxamic acid | N-Hydroxydecanamide,Decanohydroxamic acid,Caprinohydroxamic acid | |
n-Decanohydroxamic acid is a biochemical. | |||
T14043 | 4-(tert-Butyl)-benzhydroxamic Acid | Others | |
4-(tert-Butyl)-benzhydroxamic Acid is a PqsR antagonist with IC50s of 12.5 μM and 23.6 μM for E. coli and P. aeruginosa, respectively, and it reduces the production of the virulence factor pyocyanin in P. aeruginosa with... | |||
TQ0052 | SH5-07 | STAT | |
SH5-07 is a hydroxamic acid-based Stat3 inhibitor (IC50: 3.9 μM). | |||
T0721 | Piroctone olamine | Piroctone ethanolamine | Antibiotic , Antifungal |
Piroctone olamine (Piroctone ethanolamine) is a compound sometimes used in the treatment of fungal infections. Piroctone olamine is the ethanolamine salt of the hydroxamic acid derivative piroctone. | |||
T8517 | Belinostat | PX105684,PXD101,PXD-101 | HDAC , Autophagy |
Belinostat (PXD101) is an inhibitor of hydroxamic acid-type histone deacetylase (HDAC, IC50 of 27 nM in HeLa cell extracts),and with antineoplastic activity. | |||
T16729 | Remetinostat | SHP-141 | HDAC |
Remetinostat (SHP-141), a hydroxamic acid-based inhibitor of histone deacetylase enzymes, is currently being developed for the treatment of cutaneous T-cell lymphoma. | |||
T1852 | Rac-Belinostat | NSC726630,PXD101,PX-105684 | HDAC |
Rac-Belinostat (PX-105684) is a novel hydroxamic acid-type histone deacetylase (HDAC) inhibitor with antineoplastic activity. Belinostat targets HDAC enzymes, thereby inhibiting tumor cell proliferation, inducing apoptos... | |||
T33551 | N(alpha)-Acetylfusarinines | Nalpha-Acetylfusarinines | |
N(alpha)-Acetylfusarinines is a group of naturally occurring hydroxamic acids produced by unidentified species of Penicillium when grown on iron-deficient media. | |||
T68085 | Idrapril | ||
Idrapril,an angiotensin-converting enzyme (ACE) inhibitor acts by binding the catalytically important zinc ion to a hydroxamic group. | |||
T74166 | Microtubule destabilizing agent-1 | ||
Microtubule destabilizing agent-1 (Compound 12b), a hydroxamic acid-based microtubule destabilizing agent (MDA), exhibits potent antitumor activity, favorable metabolic stability, and high bioavailability, making it a pr... | |||
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 deriva... | |||
T71110 | Nanatinostat TFA | ||
Nanatinostat, also known as Tractinostat, CHR-3996 and VRx-3996, is an orally bioavailable, second-generation hydroxamic acid-based inhibitor of histone deacetylase (HDAC) with potential antineoplastic activity. HDAC inh... | |||
T36110 | L-Pyrohomoglutamic Acid | ||
L-Pyrohomoglutamic acid is an amino acid building block.1,2It has been used in the synthesis of ligands for FK506-binding proteins (FKBPs) and histone deacetylase (HDAC) inhibitors. 1.Pomplun, S., Wang, Y., Kirschner, A.... |