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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
35 Results for "
Geranyl
" in MedChemExpress (MCE) Product Catalog:
Products (35)
35 Results for "Geranyl" in MCE Product Catalog:
Cat. No.: HY-N1834
CAS No.: 246266-38-6
Category:
Target:
Cat. No.: HY-N17367
CAS No.: 1245649-15-3
Category:
Target:
Cat. No.: HY-E71074
Target:
Research Areas:
(4S)-β-Phellandrene synthase (geranyl-diphosphate-cyclizing) (EC 4.2.3.52) requires Mn2+. Mg2+ is not effective. (4S)-β-Phellandrene synthase (geranyl-diphosphate-cyclizing) (EC 4.2.3.52) n involves a 1,3-hydride shift.
Cat. No.: HY-N17265
CAS No.: 84534-32-7
Synonyms: Geranyl 1-O-α-L-arabinofuranosyl (1→6)-β-D-glucopyranoside
Cat. No.: HY-E71834
Target:
Research Areas:
4-Hydroxybenzoate geranyltransferase (EC 2.5.1.93) is a transferase that can convert 4-hydroxybenzoate and (2E)-geranyl diphosphate into 3-geranyl-4-hydroxybenzoate and diphosphate.
Cat. No.: HY-E72005
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7-Geranyloxy-5-hydroxy-2-methoxy-3-methylnaphthalene-1,4-dione synthase (EC 2.5.1.125) is a transferase that can convert 2-O,3-dimethylflaviolin, (2E)-geranyl diphosphate and H + into 7-O-geranyl- 2-O,3-dimethylflaviolin and diphosphate.
Cat. No.: HY-N19726
CAS No.: 121924-06-9
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Cat. No.: HY-E71252
Target:
Research Areas:
α-Seco-amyrin synthase (EC 5.4.99.52) requires Mg2+. Mn2+ is less effective. The enzyme will also use (3R)-linalyl diphosphate. The reaction involves a 1,2-hydride shift. The 1-pro-S hydrogen of geranyl diphosphate is lost.
Cat. No.: HY-E71347
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Research Areas:
γ-Terpinene synthase (EC 4.2.3.114) requires Mg2+. Mn2+ less effective. The reaction involves a 1,2-hydride shift. The 5-pro-S hydrogen of geranyl diphosphate is lost. Traces of several other monoterpenoids are formed in addition to γ-Terpinene.
Cat. No.: HY-E71972
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Research Areas:
6-Linalyl-2-O,3-dimethylflaviolin synthase (EC 2.5.1.124) is a transferase that can convert 2-O,3-dimethylflaviolin and (2E)-geranyl diphosphate into 6-linalyl-2-O,3-dimethylflaviolin and diphosphate.
Cat. No.: HY-P811988
Synonyms: RABGGTB; Rab GeranylGeranyltransferase Subunit Beta; Type II Protein Geranyl-Geranyltransferase Subunit Beta; GeranylGeranyl Transferase Type-2 Subunit Beta; Rab GG Transferase Beta; Rab GGTase Beta; GGTase-II-Beta; EC 2.5.1.60; GGTB; GeranylGeranyl Transferase Type II Subunit Beta; Rab Geranyl-Geranyltransferase Subunit Beta; Rab GeranylGeranyltransferase Beta Subunit
Cat. No.: HY-P811988A
Synonyms: RABGGTB; Rab GeranylGeranyltransferase Subunit Beta; Type II Protein Geranyl-Geranyltransferase Subunit Beta; GeranylGeranyl Transferase Type-2 Subunit Beta; Rab GG Transferase Beta; Rab GGTase Beta; GGTase-II-Beta; EC 2.5.1.60; GGTB; GeranylGeranyl Transferase Type II Subunit Beta; Rab Geranyl-Geranyltransferase Subunit Beta; Rab GeranylGeranyltransferase Beta Subunit
Cat. No.: HY-P701885
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: FNTA; Type I Protein Geranyl-Geranyltransferase Subunit Alpha; Farnesyltransferase, CAAX Box, Subunit Alpha; CAAX Farnesyltransferase Subunit Alpha; Protein Farnesyltransferase/GeranylGeranyltransferase Type-1 Subunit Alpha; Farnesyltransferase, CAAX Box,
Species:
Human
Source:
E. coli
Cat. No.: HY-E71324
Target:
Research Areas:
β-Primeverosidase (EC 3.2.1.149) is responsible for the formation of the alcoholic aroma in oolong and black tea. In addition to β-primeverosides [i.e. 6-O-(β-D-xylopyranosyl)-β-D-glucopyranosides], it also hydrolyses 6-O-(β-D-apiofuranosyl)-β-D-glucopyranosides and, less rapidly, β-vicianosides and 6-O-(α-L-arabinofuranosyl)-β-D-glucopyranosides, but not β-glucosides. Geranyl-, linaloyl-, benzyl-and p-nitrophenol glycosides are all hydrolysed.
Cat. No.: HY-P701886
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: FNTA; Type I Protein Geranyl-Geranyltransferase Subunit Alpha; Farnesyltransferase, CAAX Box, Subunit Alpha; CAAX Farnesyltransferase Subunit Alpha; Protein Farnesyltransferase/GeranylGeranyltransferase Type-1 Subunit Alpha; Farnesyltransferase, CAAX Box,
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
