(1S,2S,4aR,4bR,7S,9aS,10S,10aR)-2,7-Dihydroxy-1-methyl-8-methylene-13-oxododecahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid
97%
- Product Code: 96537
CAS:
545-97-1
Molecular Weight: | 348.39 g./mol | Molecular Formula: | C₁₉H₂₄O₆ |
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EC Number: | MDL Number: | MFCD00221618 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry due to its complex structure and potential bioactive properties. Its unique framework makes it a candidate for the development of novel therapeutic agents, particularly in targeting inflammatory pathways. Researchers are exploring its efficacy in modulating specific enzymes or receptors involved in inflammatory diseases, such as arthritis or asthma. Additionally, its carboxylic acid group allows for further chemical modifications, enabling the creation of derivatives with enhanced pharmacological properties. This chemical is also of interest in natural product synthesis, serving as a model for studying biosynthetic pathways and developing synthetic analogs with improved stability or activity. Its application extends to drug discovery programs, where it is screened for potential anticancer, antimicrobial, or antiviral activities.
Product Specification:
Test | Specification |
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APPEARANCE | White to Off-white Solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | £244.06 |
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(1S,2S,4aR,4bR,7S,9aS,10S,10aR)-2,7-Dihydroxy-1-methyl-8-methylene-13-oxododecahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry due to its complex structure and potential bioactive properties. Its unique framework makes it a candidate for the development of novel therapeutic agents, particularly in targeting inflammatory pathways. Researchers are exploring its efficacy in modulating specific enzymes or receptors involved in inflammatory diseases, such as arthritis or asthma. Additionally, its carboxylic acid group allows for further chemical modifications, enabling the creation of derivatives with enhanced pharmacological properties. This chemical is also of interest in natural product synthesis, serving as a model for studying biosynthetic pathways and developing synthetic analogs with improved stability or activity. Its application extends to drug discovery programs, where it is screened for potential anticancer, antimicrobial, or antiviral activities.
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