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Results for "

camphor

" in MedChemExpress (MCE) Product Catalog:

29

Inhibitors & Agonists

3

Biochemical Assay Reagents

14

Natural
Products

2

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-N0808
    Camphor
    2 Publications Verification

    (±)-camphor

    		 TRP Channel Influenza Virus Infection Inflammation/Immunology Cancer
    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 .
    Camphor
  • HY-N0808R
    Camphor (Standard)

    (±)-camphor (Standard)

    		 Reference Standards TRP Channel Influenza Virus Infection Inflammation/Immunology Cancer
    Camphor (Standard) is the analytical standard of Camphor. This product is intended for research and analytical applications. 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 .
    Camphor (Standard)
  • HY-W587405
    Camphor sulfonic acid methyl ester

    Methyl (1S)-(+)-10-camphorsulfonate

    		 Drug Intermediate Others
    Camphor sulfonic acid methyl ester (Methyl (1S)-(+)-10-camphorsulfonate) is a Camphor (HY-N0808) impurity.
    Camphor sulfonic acid methyl ester
  • HY-122808
    (-)-Camphoric acid

    		mGluR NF-κB AP-1 Metabolic Disease
    (-)-Camphoric acid is the less active enantiomer of Camphoric acid. Camphoric acid induces glutamate receptor expression. Camphoric acid also significantly induces the activation of NF-κB and AP-1. Camphoric acid significantly stimulates the differentiation of mouse osteoblastic MC3T3-E1 subclone 4 cells. Camphoric acid has weak regulatory function towards glutamate receptors. Camphoric acid can induce mRNA expression of glutamate signaling molecules and activate transcription factors, thereby stimulating osteoblast differentiation .
    (-)-Camphoric acid
  • HY-B1173
    (+)-Camphor

    D-(+)-camphor; (1R)-(+)-camphor

    		 Bacterial Neurological Disease Inflammation/Immunology Cancer
    (+)-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 .
    (+)-Camphor
  • HY-W012218
    (±)-Camphor-10-sulfonic acid

    (±)-10-camphorsulfonic acid

    		 Biochemical Assay Reagents Others
    (±)-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 .
    (±)-Camphor-10-sulfonic acid
  • HY-W015579
    (-)-Camphor

    		TRP Channel Others
    (-)-Camphor is a natural product that can be isolated from A. rnexicana .
    (-)-Camphor
  • HY-B1173R
    (+)-Camphor (Standard)

    D-(+)-camphor (Standard); (1R)-(+)-camphor (Standard)

    		 Reference Standards Bacterial Neurological Disease Inflammation/Immunology Cancer
    (+)-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 .
    (+)-Camphor (Standard)
  • HY-N12039
    Juniper camphor

    		Others Others
    Juniper camphor is a sesquiterpene compound isolated from camphor blue oil, the high-boiling fraction of camphor .
    Juniper camphor
  • HY-W012218R
    (±)-Camphor-10-sulfonic acid (Standard)

    (±)-10-camphorsulfonic acid (Standard)

    		 Reference Standards Biochemical Assay Reagents Others
    (±)-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 .
    (±)-Camphor-10-sulfonic acid (Standard)
  • HY-Y0606
    (+)-Camphor-10-sulfonic acid

    (+)-10-camphorsulfonic acid

    		 Lipase Metabolic Disease
    (+)-Camphor-10-sulfonic acid ((+)-10-Camphorsulfonic acid) is an effective pancreatic lipase (PL) inhibitor. (+)-Camphor-10-sulfonic acid is promising for research of obesity .
    (+)-Camphor-10-sulfonic acid
  • HY-17587S
    4-Methylbenzylidene camphor-d4

    		Cholinesterase (ChE) Others
    4-Methylbenzylidene camphor-d4 is the deuterium labeled 4-Methylbenzylidene camphor .
    4-Methylbenzylidene camphor-d4
  • HY-Y0848R
    (R)-Camphor-10-sulfonic acid (Standard)

    		Reference Standards
    (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.
    (R)-Camphor-10-sulfonic acid (Standard)
  • HY-17587
    4-Methylbenzylidene camphor
    2 Publications Verification

    4-MBC; Enzacamene

    		 Apoptosis PI3K Akt ERK Metabolic Disease
    4-Methylbenzylidene camphor (4-MBC) is an endocrine disrupter that produces estrogen-like effects. 4-Methylbenzylidene camphor decreases the proliferation of human trophoblast cells and induces apoptosis. 4-Methylbenzylidene camphor activates PI3K/AKT and ERK1/2 signaling pathways and elevates intracellular ROS production. 4-Methylbenzylidene camphor is a ultraviolet (UV) filter and may hamper normal placental formation during early pregnancy .
    4-Methylbenzylidene camphor
  • HY-W127838
    (+)-3-(Trifluoroacetyl)camphor

    		Biochemical Assay Reagents Others
    (+)-3-(Trifluoroacetyl)camphor is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    (+)-3-(Trifluoroacetyl)camphor
  • HY-17587R
    4-Methylbenzylidene camphor (Standard)

    4-MBC (Standard); Enzacamene (Standard)

    		 Reference Standards Apoptosis PI3K Akt ERK Metabolic Disease
    4-Methylbenzylidene camphor (Standard) is the analytical standard of 4-Methylbenzylidene camphor. This product is intended for research and analytical applications. 4-Methylbenzylidene camphor (4-MBC) is an endocrine disrupter that produces estrogen-like effects. 4-Methylbenzylidene camphor decreases the proliferation of human trophoblast cells and induces apoptosis. 4-Methylbenzylidene camphor activates PI3K/AKT and ERK1/2 signaling pathways and elevates intracellular ROS production. 4-Methylbenzylidene camphor is a ultraviolet (UV) filter and may hamper normal placental formation during early pregnancy .
    4-Methylbenzylidene camphor (Standard)
  • HY-N0278A
    (Rac)-Anemonin

    (Rac)-Pulsatilla camphor; (Rac)-Anemonine

    		 PKC NO Synthase Inflammation/Immunology
    (Rac)-Anemonin ((Rac)-Pulsatilla camphor) is the diastereoisomer of Anemonin (HY-N0278). Anemonin (Pulsatilla camphor), a selective iNOS inhibitor, is also a PKC-θ inhibitor. Anemonin can significantly inhibit the translation or protein stability of PKC-θ protein. Anemonin also ameliorates dextran sodium sulfate-induced acute ulcerative colitis (UC) in mice. Anemonin can be used in the research of inflammation-related diseases .
    (Rac)-Anemonin
  • HY-114771
    α-Truxillic acid

    		Drug Intermediate Inflammation/Immunology
    α-Truxillic acid is form by the dimerization of two molecules of α-trans-cinnamic acid, with anti-inflammatory activities. α-Truxillic acid has no analgesic activity, but its derivatives bound to camphor fragments exhibit significant activity in the peripheral analgesic model (writhing test) .
    α-Truxillic acid
  • HY-N0278
    Anemonin

    Pulsatilla camphor; Anemonine; trans-Anemonin

    		 PKC NO Synthase Inflammation/Immunology
    Anemonin (Pulsatilla camphor), a selective iNOS inhibitor, is also a PKC-θ inhibitor. Anemonin can significantly inhibit the translation or protein stability of PKC-θ protein. Anemonin also ameliorates dextran sodium sulfate-induced acute ulcerative colitis (UC) in mice. Anemonin can be used in the research of inflammation-related diseases .
    Anemonin
  • HY-N0038
    Alantolactone
    Maximum Cited Publications
    9 Publications Verification

    (+)-Alantolactone; Alant camphor; Inula camphor

    		 STAT Apoptosis TGF-beta/Smad Cancer
    Alantolactone is a selective STAT3 inhibitor, with potent anticancer activity. Alantolactone induces apoptosis in cancer .
    Alantolactone
  • HY-N0038R
    Alantolactone (Standard)

    (+)-Alantolactone (Standard); Alant camphor (Standard); Inula camphor (Standard)

    		 Reference Standards STAT Apoptosis TGF-beta/Smad Cancer
    Alantolactone (Standard) is the analytical standard of Alantolactone. This product is intended for research and analytical applications. Alantolactone is a selective STAT3 inhibitor, with potent anticancer activity. Alantolactone induces apoptosis in cancer .
    Alantolactone (Standard)
  • HY-B0900
    Anethole
    2 Publications Verification

    Anise camphor; p-Propenylanisole; Isoestragole

    		 Apoptosis Fungal Bacterial MMP NF-κB Infection Neurological Disease Inflammation/Immunology Cancer
    Anethole is a type of orally active aromatic compound that is widely found in nature and used as a flavoring agent. Anethole possesses anticancer, anti-inflammatory, antioxidant, antibacterial, antifungal, anesthetic, estrogenic, central nervous system depressant, hypnotic, insecticidal, and gastroprotective effects. Anethole can be used in the study of oxidative stress-related skin diseases and prostate cancer .
    Anethole
  • HY-N0367
    Trans-Anethole
    2 Publications Verification

    (E)​-Anethole

    		 Endogenous Metabolite Cardiovascular Disease Metabolic Disease Endocrinology Cancer
    Trans-Anethole ((E)-Anethole) is an orally active phenylpropene derivative found in Foeniculum vulgare that is estrogenic at low concentrations and cytotoxic at high concentrations in tumor cell lines. Trans-Anethole also has anti-aflatoxin, anti-thrombotic and anti-diabetic activities. Trans-Anethole is an important odor component in plants such as fennel, myrtle, liquorice, and camphor .
    Trans-Anethole
  • HY-16182
    Ecamsule
    1 Publications Verification

    		 Biochemical Assay Reagents Others
    Ecamsule is a broad-spectrum UVA filter that can be used in sunscreen product. Ecamsule reduces biological damage caused by solar radiation such as pyrimidine dimer formation, p53 protein accumula-tion, or collagenase 2 expression. Ecamsule has the potential for the research of polymorphous light eruption (PMLE) .
    Ecamsule
  • HY-16182R
    Ecamsule (Standard)

    		Biochemical Assay Reagents Reference Standards Others
    Ecamsule (Standard) is the analytical standard of Ecamsule. This product is intended for research and analytical applications. Ecamsule is a broad-spectrum UVA filter that can be used in sunscreen product. Ecamsule reduces biological damage caused by solar radiation such as pyrimidine dimer formation, p53 protein accumula-tion, or collagenase 2 expression. Ecamsule has the potential for the research of polymorphous light eruption (PMLE) .
    Ecamsule (Standard)
  • HY-16182A
    Ecamsule disodium
    1 Publications Verification

    		 Biochemical Assay Reagents Others
    Ecamsule disodium is a broad-spectrum UVA filter that can be used in sunscreen product. Ecamsule reduces biological damage caused by solar radiation such as pyrimidine dimer formation, p53 protein accumula-tion, or collagenase 2 expression .
    Ecamsule disodium
  • HY-N0367R
    Trans-Anethole (Standard)

    (E)​-Anethole (Standard)

    		 Reference Standards Endogenous Metabolite Cardiovascular Disease Metabolic Disease Endocrinology Cancer
    Trans-Anethole (Standard) is the analytical standard of Trans-Anethole. This product is intended for research and analytical applications. Trans-Anethole ((E)-Anethole) is an orally active phenylpropene derivative found in Foeniculum vulgare that is estrogenic at low concentrations and cytotoxic at high concentrations in tumor cell lines. Trans-Anethole also has anti-aflatoxin, anti-thrombotic and anti-diabetic activities. Trans-Anethole is an important odor component in plants such as fennel, myrtle, liquorice, and camphor .
    Trans-Anethole (Standard)
  • HY-N0367S
    Trans-Anethole-d3

    (E)​-Anethole-d3

    		 Isotope-Labeled Compounds Endogenous Metabolite Endocrinology
    Trans-Anethole-d3 is deuterated labeled Trans-Anethole (HY-N0367). Trans-Anethole ((E)-Anethole) is an orally active phenylpropene derivative found in Foeniculum vulgare that is estrogenic at low concentrations and cytotoxic at high concentrations in tumor cell lines. Trans-Anethole also has anti-aflatoxin, anti-thrombotic and anti-diabetic activities. Trans-Anethole is an important odor component in plants such as fennel, myrtle, liquorice, and camphor .
    Trans-Anethole-d3
  • HY-155372
    α-Glucosidase-IN-39

    		Glycosidase Metabolic Disease
    α-Glucosidase-IN-39 is a potent inhibitor of α-glucosidase enzyme with an IC50 of 869.06 ppm. α-Glucosidase-IN-39 can used in study antidiabetic .
    α-Glucosidase-IN-39

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