Cas no 1360968-74-6 (5-methyl-1h-indazol-4-ol)
5-methyl-1h-indazol-4-ol Chemical and Physical Properties
Names and Identifiers
-
- 5-methyl-1h-indazol-4-ol
- CS-0050443
- 1360968-74-6
- P17648
- AKOS027424967
- AS-54225
- SB16390
- 5-methyl-1,2-dihydroindazol-4-one
- MFCD22689684
-
- MDL: MFCD22689684
- Inchi: 1S/C8H8N2O/c1-5-2-3-7-6(8(5)11)4-9-10-7/h2-4,11H,1H3,(H,9,10)
- InChI Key: AYQJQJPZYLGUPN-UHFFFAOYSA-N
- SMILES: OC1=C(C)C=CC2=C1C=NN2
Computed Properties
- Exact Mass: 148.063662883g/mol
- Monoisotopic Mass: 148.063662883g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 11
- Rotatable Bond Count: 0
- Complexity: 151
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.6
- Topological Polar Surface Area: 48.9?2
5-methyl-1h-indazol-4-ol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | M013730-25mg |
5-Methyl-1H-indazol-4-ol |
1360968-74-6 | 25mg |
$ 150.00 | 2022-06-04 | ||
| TRC | M013730-50mg |
5-Methyl-1H-indazol-4-ol |
1360968-74-6 | 50mg |
$ 250.00 | 2022-06-04 | ||
| abcr | AB511183-100 mg |
5-Methyl-1H-indazol-4-ol; . |
1360968-74-6 | 100MG |
€246.20 | 2022-02-28 | ||
| abcr | AB511183-250 mg |
5-Methyl-1H-indazol-4-ol; . |
1360968-74-6 | 250mg |
€479.00 | 2023-06-14 | ||
| abcr | AB511183-500 mg |
5-Methyl-1H-indazol-4-ol; . |
1360968-74-6 | 500MG |
€747.40 | 2022-02-28 | ||
| Chemenu | CM238341-100mg |
5-Methyl-1H-indazol-4-ol |
1360968-74-6 | 97% | 100mg |
$151 | 2023-02-18 | |
| Chemenu | CM238341-250mg |
5-Methyl-1H-indazol-4-ol |
1360968-74-6 | 97% | 250mg |
$301 | 2023-02-18 | |
| Chemenu | CM238341-500mg |
5-Methyl-1H-indazol-4-ol |
1360968-74-6 | 97% | 500mg |
$503 | 2023-02-18 | |
| Chemenu | CM238341-5g |
5-Methyl-1H-indazol-4-ol |
1360968-74-6 | 97% | 5g |
$2264 | 2023-02-18 | |
| eNovation Chemicals LLC | D588841-100mg |
5-methyl-1H-indazol-4-ol |
1360968-74-6 | 97% | 100mg |
$220 | 2024-07-21 |
5-methyl-1h-indazol-4-ol Related Literature
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Guang Xu,Wei Zhang,Ying Zhang,Xiaoxia Zhao,Ping Wen,Di Ma RSC Adv., 2018,8, 19353-19361
-
Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
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Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
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Andreas Nenning,Manuel Holzmann,Jürgen Fleig,Alexander K. Opitz Mater. Adv., 2021,2, 5422-5431
-
Max Attwood,Hiroki Akutsu,Lee Martin,Toby J. Blundell,Pierre Le Maguere,Scott S. Turner Dalton Trans., 2021,50, 11843-11851
Additional information on 5-methyl-1h-indazol-4-ol
Recent Advances in the Study of 5-methyl-1h-indazol-4-ol (CAS: 1360968-74-6) and Its Applications in Chemical Biology and Medicine
5-methyl-1h-indazol-4-ol (CAS: 1360968-74-6) has emerged as a compound of significant interest in the field of chemical biology and medicinal chemistry. Recent studies have highlighted its potential as a versatile scaffold for the development of novel therapeutic agents, particularly in the areas of oncology and inflammation. This research briefing provides an overview of the latest findings related to this compound, focusing on its synthesis, biological activity, and potential applications.
A recent study published in the Journal of Medicinal Chemistry explored the synthesis and optimization of 5-methyl-1h-indazol-4-ol derivatives for enhanced pharmacokinetic properties. The researchers employed a multi-step synthetic route, starting from commercially available precursors, to achieve high yields and purity of the target compound. The study also investigated the compound's stability under various physiological conditions, providing valuable insights for future formulation development.
In the context of biological activity, 5-methyl-1h-indazol-4-ol has shown promising results as an inhibitor of key signaling pathways involved in cancer progression. A 2023 study in Cancer Research demonstrated that this compound effectively targets the PI3K/AKT/mTOR pathway, leading to significant inhibition of tumor growth in preclinical models. The researchers noted that the compound's unique structural features contribute to its selectivity and potency, making it a promising candidate for further development.
Another area of active research involves the application of 5-methyl-1h-indazol-4-ol in inflammatory diseases. A recent publication in Nature Communications reported that derivatives of this compound exhibit potent anti-inflammatory effects by modulating NF-κB signaling. The study utilized both in vitro and in vivo models to validate the compound's efficacy, with results suggesting potential applications in conditions such as rheumatoid arthritis and inflammatory bowel disease.
From a drug development perspective, the physicochemical properties of 5-methyl-1h-indazol-4-ol have been extensively characterized. Computational modeling studies have predicted favorable drug-like properties, including good solubility and membrane permeability. These findings, combined with the compound's demonstrated biological activity, position it as a strong candidate for lead optimization programs in pharmaceutical research.
Looking ahead, several research groups are exploring the potential of 5-methyl-1h-indazol-4-ol as a building block for more complex drug molecules. Its structural flexibility allows for diverse modifications, enabling the creation of libraries of derivatives with tailored biological activities. This approach aligns with current trends in medicinal chemistry that emphasize the importance of scaffold diversity in drug discovery.
In conclusion, the growing body of research on 5-methyl-1h-indazol-4-ol (CAS: 1360968-74-6) underscores its significance in contemporary chemical biology and medicinal chemistry. The compound's unique properties and demonstrated biological activities make it a valuable subject for ongoing research, with potential applications spanning multiple therapeutic areas. Future studies will likely focus on further optimizing its pharmacological profile and exploring its mechanisms of action in greater detail.
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