5872-08-2
5872-08-2
Chemical Structure
(±)-Camphor-10-sulfonic acid
Synonym(s): (±)-10-Camphorsulfonic acid
- CAS No.: 5872-08-2
- Formula:C10H16O4S
- Molecular Weight:232.30
IUPAC Name: (7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonic acid
InChIKey: MIOPJNTWMNEORI-UHFFFAOYSA-N
SMILES: O=C1CC2CCC1(C2(C)C)CS(=O)(O)=O
Biological Activity: (±)-Camphor-10-sulfonic acid is a racemate of Camphor-10-sulfonic acid. (±)-Camphor-10-sulfonic acid can be used as an organocatalyst in performing a huge array of organic transformations[1].
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(±)-Camphor-10-sulfonic acid | 99.83% | (±)-Camphor-10-sulfonic acid is a racemate of Camphor-10-sulfonic acid. (±)-Camphor-10-sulfonic acid can be used as an organocatalyst in performing a huge array of organic transformations. | ||||||||||||||||||||
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(±)-Camphor-10-sulfonic acid (Standard) | ≥98% | (±)-Camphor-10-sulfonic acid (Standard) is the analytical standard of (±)-Camphor-10-sulfonic acid. This product is intended for research and analytical applications. (±)-Camphor-10-sulfonic acid is a racemate of Camphor-10-sulfonic acid. (±)-Camphor-10-sulfonic acid can be used as an organocatalyst in performing a huge array of organic transformations. | ||||||||||||||||||||
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Fenchone | 96.98% | Fenchone is a natural product. | ||||||||||||||||||||
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(+)-Camphor (Standard) | ≥98% | (+)-Camphor (Standard) is the analytical standard of (+)-Camphor. This product is intended for research and analytical applications. (+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) is an isomer of Camphor. Camphor is an agonist of monoterpenoid transient receptor potential (TRP) channels (such as TRPV1, TRPV3, TRPM8) and an inhibitor of TRPA1 channels. Camphor's derivatives have multiple biological activities, including antibacterial, antiviral, antioxidant, analgesic and anticancer. Camphor can selectively activate cold-sensitive TRP channels and inhibit TRPA1-mediated nociceptive signals. Camphor stimulates the cold-sensing nerve endings in the skin and regulates the activity of ion channels to exert analgesic, anti-inflammatory and anti-itching effects. It also has anti-proliferative and anti-mutagenic activities on tumor cells, which may be related to inhibiting ribosome function or inducing cell apoptosis. Camphor can be absorbed through the skin and (+)-Camphor can be used in the study of muscle and joint pain and inflammation. | ||||||||||||||||||||
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Camphor | 98.0% | Camphor ((±)-Camphor) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. However, Camphor is poisonous when ingested. Antiviral, antitussive, and anticancer activities. Camphor is a TRPV3 agonist. | ||||||||||||||||||||
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(-)-Fenchone | 98.0% | (-)-Fenchone is a bicyclic monoterpene and serves as a substrate for human liver microsomal cytochrome P450 enzymes CYP2A6 and CYP2B6. (-)-Fenchone is not metabolized by human CYP1A1, CYP1A2, CYP1B1, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP2E1, or CYP3A4 enzymes. (-)-Fenchone undergoes hydroxylation to produce 6-exo-hydroxyfenchone, 6-endo-hydroxyfenchone, and 10-hydroxyfenchone. During the metabolism of (-)-Fenchone, CYP2A6 may play a more important role than CYP2B6. | ||||||||||||||||||||
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(-)-Camphor | 98.0% | (-)-Camphor is an enantiomer of Camphor (HY-N0808) and belongs to the class of bicyclic monoterpene ketones. Camphor ((±)-Camphor) is a topical anti-infective and antipruritic agent, and exhibits carminative effects when administered orally. However, Camphor is toxic upon ingestion. Camphor possesses antiviral, antitussive and anticancer activities. Camphor acts as a TRPV3 agonist. | ||||||||||||||||||||
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(+)-Fenchone | 99.88% | (+)-Fenchone is an antibacterial agent. (+)-Fenchone interferes with bacterial fatty acid synthesis, disrupts fungal cell wall construction, and inhibits bacterial biofilm formation. (+)-Fenchone can be used in studies related to bacterial and fungal infections. | ||||||||||||||||||||
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Camphorquinone | 97.0% | Camphorquinone (2,3-Bornanedione) is a photoinitiator. Camphorquinone enhances free radical production under visible light (VL) irradiation and exhibits minimal cytotoxicity to HPF cells. Camphorquinone is used in the research of dental resin polymers. | ||||||||||||||||||||
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(+)-(1S)-Camphorquinone | 99.70% | (+)-(1S)-Camphorquinone is an isomer of Camphorquinone (HY-W086630). (+)-(1S)-Camphorquinone can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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(+)-Camphor-10-sulfonic acid | 98% | (+)-Camphor-10-sulfonic acid ((+)-10-Camphorsulfonic acid) is a ligand of pancreatic lipase, with an IC50 of 24.8 μM against porcine pancreatic lipase. As an antagonist, (+)-Camphor-10-sulfonic acid prevents Orlistat (HY-B0218) from binding to the active site of pancreatic lipase. (+)-Camphor-10-sulfonic acid can be used in research related to obesity. | ||||||||||||||||||||
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(R)-Camphor-10-sulfonic acid (Standard) | ≥98% | (R)-Camphor-10-sulfonic acid (Standard) is the analytical standard of (R)-Camphor-10-sulfonic acid. This product is intended for research and analytical applications. | ||||||||||||||||||||
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