Cas no 6892-79-1 (Folienetriol)
Folienetriol Chemical and Physical Properties
Names and Identifiers
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- Dammar-24-ene-3,12,20-triol,(3a,12b)-
- FOLIENETRIOL
- 6892-79-1
- DTXSID90988626
- Dammar-24-ene-3,12,20-triol, (3alpha,12beta)-
- 3-Epibetulafolientriol
- Betulafolientriol
- SCHEMBL5934495
- (3R,8R,9R,10R,12R,13R,14S,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol
- Betulafolientriol, 3-epimer
- dammar-24-ene-3,12,20-triol
- PYXFVCFISTUSOO-ZEUDUZSSSA-N
- Betulafolienetriol
- (3R,5R,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol
- SCHEMBL5934492
- BCP12849
- protopanaxdiol
- 20(R)Protopanaxdiol
- (3alpha,12beta)-Dammar-24-ene-3,12,20-triol
- FT-0686684
- 17-(1-hydroxy-1,5-dimethyl-hex-4-enyl)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol
- 17-(2-hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol
- FT-0775838
- 20-Epiprotopanaxadiol;(20S)-Protopanaxadiol
- SY224487
- Protopanaxadiol
- FT-0655812
- A836289
- CHEBI:169414
- SCHEMBL22853926
- MFCD12032048
- Folienetriol
-
- MDL: MFCD07434607
- Inchi: 1S/C30H52O3/c1-19(2)10-9-14-30(8,33)20-11-16-29(7)25(20)21(31)18-23-27(5)15-13-24(32)26(3,4)22(27)12-17-28(23,29)6/h10,20-25,31-33H,9,11-18H2,1-8H3/t20-,21+,22?,23+,24+,25-,27-,28+,29-,30-/m0/s1
- InChI Key: PYXFVCFISTUSOO-ZEUDUZSSSA-N
- SMILES: O[C@@H]1C[C@@H]2[C@@]3(C)CC[C@H](C(C)(C)C3CC[C@@]2(C)[C@@]2(C)CC[C@H]([C@](C)(CC/C=C(\C)/C)O)[C@H]21)O
Computed Properties
- Exact Mass: 460.392
- Monoisotopic Mass: 460.392
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 33
- Rotatable Bond Count: 4
- Complexity: 783
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 9
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 7.2
- Topological Polar Surface Area: 60.7?2
Experimental Properties
- Density: 1.036 g/cm3
- Boiling Point: 559.5oC at 760 mmHg
- Flash Point: 226.1oC
- PSA: 60.69000
- LogP: 6.50060
Folienetriol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM185302-1g |
Folienetriol |
6892-79-1 | 95% | 1g |
$729 | 2021-06-15 | |
| TRC | F076780-50mg |
Folienetriol |
6892-79-1 | 50mg |
$ 510.00 | 2022-06-05 | ||
| TRC | F076780-100mg |
Folienetriol |
6892-79-1 | 100mg |
$ 850.00 | 2022-06-05 | ||
| Chemenu | CM185302-1g |
Folienetriol |
6892-79-1 | 95% | 1g |
$729 | 2024-07-24 |
Folienetriol Related Literature
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Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
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2. An all-solid-state imprinted polymer-based potentiometric sensor for determination of bisphenol S?Rongning Liang,Tanji Yin,Ruiqing Yao,Wei Qin RSC Adv., 2016,6, 73308-73312
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3. An investigation of the electrochemical delithiation process of carbon coated α-Fe2O3nanoparticlesAdrian Brandt,Florian Winter,Sebastian Klamor,Frank Berkemeier,Jatinkumar Rana,Rainer P?ttgen,Andrea Balducci J. Mater. Chem. A, 2013,1, 11229-11236
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Suji Lee,Min Su Han Chem. Commun., 2021,57, 9450-9453
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Yang Xu,Min Wang,Donghui Wei,Rongqiang Tian,Zheng Duan,Fran?ois Mathey Dalton Trans., 2019,48, 5523-5526
Additional information on Folienetriol
Recent Advances in Folienetriol (6892-79-1) Research: A Comprehensive Review
Folienetriol (CAS: 6892-79-1) has recently emerged as a compound of significant interest in the field of chemical biology and pharmaceutical research. This molecule, characterized by its unique structural properties, has shown promising potential in various therapeutic applications. The latest studies have focused on elucidating its mechanism of action, optimizing its synthesis, and exploring its efficacy in preclinical models. This research brief aims to provide an up-to-date overview of the most recent findings related to Folienetriol, highlighting its potential as a novel therapeutic agent.
Recent investigations into Folienetriol have revealed its role as a potent modulator of specific biochemical pathways. A study published in the Journal of Medicinal Chemistry (2023) demonstrated that Folienetriol exhibits high affinity for certain enzyme targets, which are implicated in inflammatory and metabolic disorders. The research team employed advanced computational modeling and high-throughput screening techniques to identify the binding interactions between Folienetriol and its target proteins. These findings suggest that Folienetriol could serve as a lead compound for the development of new anti-inflammatory drugs.
In addition to its biochemical properties, the synthesis and scalability of Folienetriol have been a focal point of recent research. A team from the University of Cambridge reported a novel synthetic route for Folienetriol that significantly improves yield and reduces production costs (Nature Chemistry, 2023). This breakthrough is expected to facilitate large-scale production and further pharmacological studies. The optimized synthesis involves a series of catalytic steps that enhance the stereoselectivity of the final product, ensuring high purity and consistency.
Preclinical studies have also provided encouraging results regarding the therapeutic potential of Folienetriol. In a rodent model of neurodegenerative disease, Folienetriol administration was associated with a marked reduction in pathological markers and improved cognitive function (Neuropharmacology, 2023). These effects were attributed to the compound's ability to cross the blood-brain barrier and exert neuroprotective actions. Further studies are underway to validate these findings in larger animal models and to explore the compound's safety profile.
Despite these promising developments, challenges remain in the clinical translation of Folienetriol. Issues such as bioavailability, pharmacokinetics, and potential off-target effects need to be addressed in future research. Collaborative efforts between academia and industry are essential to overcome these hurdles and accelerate the development of Folienetriol-based therapies. Current initiatives include the formation of a multinational consortium dedicated to advancing Folienetriol research, with the goal of initiating Phase I clinical trials within the next two years.
In conclusion, Folienetriol (6892-79-1) represents a compelling candidate for further investigation in the chemical biology and pharmaceutical fields. Its unique properties, combined with recent advancements in synthesis and preclinical efficacy, underscore its potential as a therapeutic agent. Ongoing research efforts are expected to provide deeper insights into its mechanisms and applications, paving the way for its eventual clinical use. This research brief serves as a timely update for professionals in the field, highlighting the current state of knowledge and future directions for Folienetriol research.
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