Cas no 1310693-92-5 (Tubastatin A hydrochloride)
Tubastatin A hydrochloride Chemical and Physical Properties
Names and Identifiers
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- Tubastatin A hydrochloride
- Tubastatin A HCl
- N-Hydroxy-4-[(2-methyl-1,2,3,4-tetrahydro-5H-pyrido[4,3-b]indol-5 -yl)methyl]benzamide hydrochloride (1:1)
- Tubastatin A Hydroch
- Tubastatin A Hydrochloride (Also See: T897000)
- Tubastatin A Hydrochloride(Also See: T897000)
- TSA HCl
- N-Hydroxy-4-[[2-methyl-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl]methyl]benzamide Hydrochloride
- N-Hydroxy-4-[(1,2,3,4-tetrahydro-2-methyl-5H-pyrido[4,3-b]indol-5-yl)methyl]benzamide hydrochloride
-
- MDL: MFCD20488052
- Inchi: 1S/C20H21N3O2.ClH/c1-22-11-10-19-17(13-22)16-4-2-3-5-18(16)23(19)12-14-6-8-15(9-7-14)20(24)21-25;/h2-9,25H,10-13H2,1H3,(H,21,24);1H
- InChI Key: LJTSJTWIMOGKRJ-UHFFFAOYSA-N
- SMILES: Cl.O=C(C1C=CC(=CC=1)CN1C2C=CC=CC=2C2CN(C)CCC1=2)NO
Computed Properties
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 26
- Rotatable Bond Count: 4
Tubastatin A hydrochloride Security Information
- Signal Word:Warning
- Hazard Statement: H302-H315-H319-H335
- Warning Statement: P261-P305+P351+P338
- Storage Condition:<0°C
Tubastatin A hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| S e l l e c k ZHONG GUO | S2627-10mM (1mL in DMSO) |
Tubastatin A HCl |
1310693-92-5 | 99.30% | 10mM (1mL in DMSO) |
¥1306.88 | 2023-09-15 | |
| S e l l e c k ZHONG GUO | S2627-10mg |
Tubastatin A HCl |
1310693-92-5 | 99.30% | 10mg |
¥977.38 | 2023-09-15 | |
| S e l l e c k ZHONG GUO | S2627-50mg |
Tubastatin A HCl |
1310693-92-5 | 99.30% | 50mg |
RMB2191.16 | 2021-07-13 | |
| S e l l e c k ZHONG GUO | S2627-100mg |
Tubastatin A HCl |
1310693-92-5 | 99.30% | 100mg |
¥3864.75 | 2023-09-15 | |
| S e l l e c k ZHONG GUO | S2627-200mg |
Tubastatin A HCl |
1310693-92-5 | 99.30% | 200mg |
¥7127.94 | 2022-04-26 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | T129677-10mg |
Tubastatin A hydrochloride |
1310693-92-5 | ≥98% | 10mg |
¥378.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | T129677-250mg |
Tubastatin A HCl |
1310693-92-5 | ≥98% | 250mg |
¥2,280.00 | 2021-05-25 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | T129677-50mg |
Tubastatin A hydrochloride |
1310693-92-5 | ≥98% | 50mg |
¥667.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | T129677-5mg |
Tubastatin A hydrochloride |
1310693-92-5 | ≥98% | 5mg |
¥223.90 | 2023-08-31 | |
| DC Chemicals | DC6303-100 mg |
Tubastatin A HCl |
1310693-92-5 | >98% | 100mg |
$300.0 | 2022-02-28 |
Tubastatin A hydrochloride Suppliers
Tubastatin A hydrochloride Related Literature
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
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Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
Additional information on Tubastatin A hydrochloride
Comprehensive Overview of Tubastatin A Hydrochloride (CAS No. 1310693-92-5): Mechanism, Applications, and Research Insights
Tubastatin A hydrochloride (CAS No. 1310693-92-5) is a highly selective and potent inhibitor of histone deacetylase 6 (HDAC6), a key enzyme involved in epigenetic regulation and cellular homeostasis. With its molecular formula C20H21N3O2·HCl, this compound has garnered significant attention in biomedical research due to its unique specificity for HDAC6 over other HDAC isoforms. Researchers frequently search for terms like "HDAC6 inhibitor", "Tubastatin A solubility", and "Tubastatin A vs. other HDAC inhibitors", reflecting its growing relevance in drug discovery and disease modeling.
The mechanism of action of Tubastatin A hydrochloride centers on its ability to modulate α-tubulin acetylation, a process critical for cytoskeletal stability and intracellular transport. Unlike pan-HDAC inhibitors, Tubastatin A exhibits minimal off-target effects, making it a preferred tool for studying HDAC6-dependent pathways. Recent studies highlight its potential in addressing neurodegenerative diseases, cancer immunotherapy, and inflammatory disorders—topics trending in scientific forums and AI-driven literature searches. Questions such as "Can Tubastatin A cross the blood-brain barrier?" or "Tubastatin A clinical trials 2023" underscore its translational potential.
From a biochemical perspective, Tubastatin A hydrochloride demonstrates an IC50 of ~15 nM for HDAC6, with >1,000-fold selectivity over HDAC1. This precision enables researchers to dissect HDAC6's role in aggresome formation and protein degradation without confounding results from other HDACs. Its application extends to ChIP-seq and proteomics studies, where users often inquire about "Tubastatin A protocol for cell culture" or "optimal dosage for in vivo studies". The compound's stability in aqueous solutions (pH 3–7) and bioavailability further enhance its utility.
Emerging trends link Tubastatin A hydrochloride to autophagy modulation and immune checkpoint regulation, areas dominating recent PubMed citations. Notably, its synergy with PARP inhibitors in oncology models has sparked debates on "combination therapy strategies". The compound's hydrochloride salt form (CAS 1310693-92-5) ensures improved solubility for experimental reproducibility—a detail frequently queried in researchgate discussions.
Quality control parameters for Tubastatin A hydrochloride typically include HPLC purity (>98%), mass spectrometry validation, and endotoxin testing. These metrics address common purchaser concerns like "how to verify Tubastatin A authenticity" or "storage conditions for long-term stability". As the scientific community pivots toward targeted epigenetic therapies, this compound remains at the forefront of translational research, bridging gaps between bench findings and therapeutic innovation.
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