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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
21 Results for "
farnesol
" in MedChemExpress (MCE) Product Catalog:
Products (21)
21 Results for "farnesol" in MCE Product Catalog:
2
16
16 Publications Verification
Cat. No.: HY-16343
CAS No.: 131060-14-5
Target:
Research Areas:
NB-598 is a potent and competitive inhibitor of squalene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway. NB-598 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
16
16 Publications Verification
Cat. No.: HY-16343C
CAS No.: 155294-62-5
Target:
Research Areas:
NB-598 Maleate is a potent and competitive inhibitor of squalene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway. NB-598 (Maleate) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
6
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Thonzonium bromide is an antibacterial agent that is structurally similar to Farnesol (HY-Y0248A). Thonzonium bromide is also a monocationic surface-active agent, which inhibits RANKL-induced osteoclast formation and bone resorption in vitro and prevents LPS-induced bone loss in vivo. Thonzonium bromide inhibits proton transport in a dose-dependent manner (EC50=69 μM) .
Cat. No.: HY-Y0248AS
CAS No.: 166447-71-8
Synonyms: trans,trans-farnesol-d6; (2E,6E)-farnesol-d6
Cat. No.: HY-Y0248AR
CAS No.: 4602-84-0
Cat. No.: HY-W749519
Synonyms: trans,trans-farnesol-13C3; (2E,6E)-farnesol-13C3
Synonyms: trans,trans-farnesol (Standard); (2E,6E)-farnesol (Standard)
Cat. No.: HY-16343A
CAS No.: 136719-25-0
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Research Areas:
NB-598 hydrochloride is a potent and competitive inhibitor of squalene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway. NB-598 (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Cat. No.: HY-100299A
CAS No.: 190841-57-7
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Research Areas:
RPR107393 is an orally active potent selective squalene synthase (SQS) inhibitor. RPR107393 inhibits rat liver microsomal squalene synthase with an IC50 value of 0.8 nM. RPR107393 reduces triglyceride biosynthesis by suppressing fatty acid biosynthesis via an increase in intracellular farnesol and its derivatives. RPR107393 reduces plasma cholesterol in rats and marmosets. RPR107393 can be used for metabolic disease research, such as hypercholesterolemia, hypertriglyceridemia and atherosclerosis .
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Research Areas:
Thonzonium (bromide) (Standard) is the analytical standard of Thonzonium (bromide). This product is intended for research and analytical applications. Thonzonium bromide is an antibacterial agent that is structurally similar to Farnesol (HY-Y0248A). Thonzonium bromide is also a monocationic surface-active agent, which inhibits RANKL-induced osteoclast formation and bone resorption in vitro and prevents LPS-induced bone loss in vivo. Thonzonium bromide inhibits proton transport in a dose-dependent manner (EC50=69 μM) .
Cat. No.: HY-100299
CAS No.: 197576-78-6
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Research Areas:
RPR107393 free base is an orally active potent selective squalene synthase (SQS) inhibitor. RPR107393 free base inhibits rat liver microsomal squalene synthase with an IC50 value of 0.8 nM. RPR107393 free base reduces triglyceride biosynthesis by suppressing fatty acid biosynthesis via an increase in intracellular farnesol and its derivatives. RPR107393 free base reduces plasma cholesterol in rats and marmosets. RPR107393 free base can be used for metabolic disease research, such as hypercholesterolemia, hypertriglyceridemia and atherosclerosis [1][2].
Cat. No.: HY-N17654
CAS No.: 1220194-95-5
Category:
Leguminosae/Fabaceae Extract Plant Dalbergia tonkinensis Prain Extract Terpenoids Sesquiterpenes
Target:
Cat. No.: HY-N20617
CAS No.: 69809-46-7
Cat. No.: HY-N21682
CAS No.: 31769-65-0
Target:
Cat. No.: HY-P705557
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Bile acid receptor; farnesol receptor HRR-1; Nuclear receptor subfamily 1 group H member 4; Retinoid X receptor-interacting protein 14; RXR-interacting protein 14; NR1H4; FXR; BAR; HRR1; RIP14
Species:
Human
Source:
E. coli
Cat. No.: HY-P703605
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: NR1H4; farnesol Receptor HRR-1; Nuclear Receptor Subfamily 1 Group H Member 4; HRR-1; Bile Acid Receptor; RXR-Interacting Protein 14; RIP14; BAR; HRR1; Nuclear Receptor Subfamily 1, Group H, Member 4; FXR; Farnesoid X Nuclear Receptor; Retinoid X Receptor
Species:
Human
Source:
E. coli
Cat. No.: HY-P703606
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: NR1H4; farnesol Receptor HRR-1; Nuclear Receptor Subfamily 1 Group H Member 4; HRR-1; Bile Acid Receptor; RXR-Interacting Protein 14; RIP14; BAR; HRR1; Nuclear Receptor Subfamily 1, Group H, Member 4; FXR; Farnesoid X Nuclear Receptor; Retinoid X Receptor
Species:
Human
Source:
E. coli
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
