NCBI Taxonomy: 2321332

Raputia (ncbi_taxid: 2321332)

found 100 associated metabolites at genus taxonomy rank level.

Ancestor: Zanthoxyloideae

Child Taxonomies: Raputia ulei, Raputia praetermissa

Stigmasterol

(3S,8S,9S,10R,13R,14S,17R)-17-((2R,5S,E)-5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H48O (412.37049579999996)


Stigmasterol is a phytosterol, meaning it is steroid derived from plants. As a food additive, phytosterols have cholesterol-lowering properties (reducing cholesterol absorption in intestines), and may act in cancer prevention. Phytosterols naturally occur in small amount in vegetable oils, especially soybean oil. One such phytosterol complex, isolated from vegetable oil, is cholestatin, composed of campesterol, stigmasterol, and brassicasterol, and is marketed as a dietary supplement. Sterols can reduce cholesterol in human subjects by up to 15\\%. The mechanism behind phytosterols and the lowering of cholesterol occurs as follows : the incorporation of cholesterol into micelles in the gastrointestinal tract is inhibited, decreasing the overall amount of cholesterol absorbed. This may in turn help to control body total cholesterol levels, as well as modify HDL, LDL and TAG levels. Many margarines, butters, breakfast cereals and spreads are now enriched with phytosterols and marketed towards people with high cholesterol and a wish to lower it. Stigmasterol is found to be associated with phytosterolemia, which is an inborn error of metabolism. Stigmasterol is a 3beta-sterol that consists of 3beta-hydroxystigmastane having double bonds at the 5,6- and 22,23-positions. It has a role as a plant metabolite. It is a 3beta-sterol, a stigmastane sterol, a 3beta-hydroxy-Delta(5)-steroid and a member of phytosterols. It derives from a hydride of a stigmastane. Stigmasterol is a natural product found in Ficus auriculata, Xylopia aromatica, and other organisms with data available. Stigmasterol is a steroid derivative characterized by the hydroxyl group in position C-3 of the steroid skeleton, and unsaturated bonds in position 5-6 of the B ring, and position 22-23 in the alkyl substituent. Stigmasterol is found in the fats and oils of soybean, calabar bean and rape seed, as well as several other vegetables, legumes, nuts, seeds, and unpasteurized milk. See also: Comfrey Root (part of); Saw Palmetto (part of); Plantago ovata seed (part of). Stigmasterol is an unsaturated plant sterol occurring in the plant fats or oils of soybean, calabar bean, and rape seed, and in a number of medicinal herbs, including the Chinese herbs Ophiopogon japonicus (Mai men dong) and American Ginseng. Stigmasterol is also found in various vegetables, legumes, nuts, seeds, and unpasteurized milk. A 3beta-sterol that consists of 3beta-hydroxystigmastane having double bonds at the 5,6- and 22,23-positions. C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol

   

Skimmianine

4,7,8-trimethoxy-furo(2,3-b)quinoline

C14H13NO4 (259.0844538)


Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1]. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1].

   

Dictamnine

4-methoxyfuro(2,3-b)quinoline

C12H9NO2 (199.0633254)


Dictamnine (Dictamine) exhibits cytotoxicity to human cervical and colon cancer cells and also has antibacterial and antifungal activities. Dictamnine (Dictamine) exhibits cytotoxicity to human cervical and colon cancer cells and also has antibacterial and antifungal activities.

   

Maculosidine

Furo(2,3-b)quinoline, 4,6,8-trimethoxy-

C14H13NO4 (259.0844538)


   

Robustine

Furo(2,3-b)quinolin-8-ol, 4-methoxy-

C12H9NO3 (215.0582404)


A quinoline alkaloid that is furo[2,3-b]quinoline substituted by a methoxy and a hydroxy group at positions 4 and 8 respectively. Robustine, a furoquinoline alkaloid, from Dictamnus albus, exhibits inhibitory potency against human phosphodiesterase 5 (hPDE5A) in vitro[1]. Robustine, a furoquinoline alkaloid, from Dictamnus albus, exhibits inhibitory potency against human phosphodiesterase 5 (hPDE5A) in vitro[1].

   

dictamine

4-27-00-02030 (Beilstein Handbook Reference)

C12H9NO2 (199.0633254)


Dictamnine is an oxacycle, an organonitrogen heterocyclic compound, an organic heterotricyclic compound and an alkaloid antibiotic. Dictamnine is a natural product found in Haplophyllum bucharicum, Haplophyllum cappadocicum, and other organisms with data available. A furoquinoline alkaloid, dictamnine, is very common within the family Rutaceae. It is the main alkaloid in the roots of Dictamnus albus and responsible for the mutagenicity of the drug derived from crude extracts. Dictamnine was also reported to be a phototoxic and photomutagenic compound. It participates in the severe skin phototoxicity of the plant. Dictamnine (Dictamine) exhibits cytotoxicity to human cervical and colon cancer cells and also has antibacterial and antifungal activities. Dictamnine (Dictamine) exhibits cytotoxicity to human cervical and colon cancer cells and also has antibacterial and antifungal activities.

   

Skimmianine

InChI=1/C14H13NO4/c1-16-10-5-4-8-11(13(10)18-3)15-14-9(6-7-19-14)12(8)17-2/h4-7H,1-3H

C14H13NO4 (259.0844538)


Skimmianine is an organonitrogen heterocyclic compound, an organic heterotricyclic compound, an oxacycle and an alkaloid antibiotic. Skimmianine is a natural product found in Haplophyllum bucharicum, Haplophyllum cappadocicum, and other organisms with data available. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1]. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1].

   

Stigmasterol

Stigmasterol

C29H48O (412.37049579999996)


Disclaimer: While authors make an effort to ensure that the content of this record is accurate, the authors make no representations or warranties in relation to the accuracy or completeness of the record. This record do not reflect any viewpoints of the affiliation and organization to which the authors belong.

   

4-methoxy-1-methylquinolin-2-one

4-methoxy-1-methylquinolin-2-one

C11H11NO2 (189.0789746)


   

5-(4-methoxymethylfuran-2-yl)-1H-indole|5-[4-(methoxymethyl)furan-2-yl]indole|raputimonoindole C

5-(4-methoxymethylfuran-2-yl)-1H-indole|5-[4-(methoxymethyl)furan-2-yl]indole|raputimonoindole C

C14H13NO2 (227.09462380000002)


   

Skimmianine

Skimmianine

C14H13NO4 (259.0844538)


Origin: Plant; SubCategory_DNP: Alkaloids derived from anthranilic acid, Quinoline alkaloids relative retention time with respect to 9-anthracene Carboxylic Acid is 1.053 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.048 Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1]. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1].

   
   

Stigmasterin

(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methyl-hept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

C29H48O (412.37049579999996)


C1907 - Drug, Natural Product > C28178 - Phytosterol > C68437 - Unsaturated Phytosterol

   

dictamine

4-27-00-02030 (Beilstein Handbook Reference)

C12H9NO2 (199.0633254)


Dictamnine (Dictamine) exhibits cytotoxicity to human cervical and colon cancer cells and also has antibacterial and antifungal activities. Dictamnine (Dictamine) exhibits cytotoxicity to human cervical and colon cancer cells and also has antibacterial and antifungal activities.

   

Skimmianin

InChI=1\C14H13NO4\c1-16-10-5-4-8-11(13(10)18-3)15-14-9(6-7-19-14)12(8)17-2\h4-7H,1-3H

C14H13NO4 (259.0844538)


Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1]. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1].

   

[(5r,7s)-7-[(1e)-2-(1h-indol-5-yl)ethenyl]-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]methanol

[(5r,7s)-7-[(1e)-2-(1h-indol-5-yl)ethenyl]-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]methanol

C26H26N2O (382.2045026)


   

6-[(1e)-2-[(5r,7r)-5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl]-1h-indole

6-[(1e)-2-[(5r,7r)-5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl]-1h-indole

C26H26N2 (366.2095876)


   

[(5r,7s)-5-[(1e)-2-(1h-indol-5-yl)ethenyl]-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]methanol

[(5r,7s)-5-[(1e)-2-(1h-indol-5-yl)ethenyl]-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]methanol

C26H26N2O (382.2045026)


   

5-[3-(3-methylbut-2-en-1-yl)-4-methylideneoxolan-2-yl]-1h-indole

5-[3-(3-methylbut-2-en-1-yl)-4-methylideneoxolan-2-yl]-1h-indole

C18H21NO (267.1623056)


   

{7-[2-(1h-indol-5-yl)ethenyl]-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl}methanol

{7-[2-(1h-indol-5-yl)ethenyl]-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl}methanol

C26H26N2O (382.2045026)


   

pentadecyl 3-(2-hydroxy-4-methoxyphenyl)prop-2-enoate

pentadecyl 3-(2-hydroxy-4-methoxyphenyl)prop-2-enoate

C25H40O4 (404.29264400000005)


   

5-[4-(methoxymethyl)furan-2-yl]-1h-indole

5-[4-(methoxymethyl)furan-2-yl]-1h-indole

C14H13NO2 (227.09462380000002)


   

6-[(1z)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

6-[(1z)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

C26H26N2 (366.2095876)


   

6-[(1e)-2-[(5s,7s)-5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl]-1h-indole

6-[(1e)-2-[(5s,7s)-5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl]-1h-indole

C26H26N2 (366.2095876)


   

methyl 5-(1h-indol-5-yl)furan-3-carboxylate

methyl 5-(1h-indol-5-yl)furan-3-carboxylate

C14H11NO3 (241.0738896)


   

7-[(1e)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

7-[(1e)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

C26H26N2 (366.2095876)


   

hexadecyl (2e)-3-(2-hydroxy-4-methoxyphenyl)prop-2-enoate

hexadecyl (2e)-3-(2-hydroxy-4-methoxyphenyl)prop-2-enoate

C26H42O4 (418.30829320000004)


   

7-{2-[7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-1h-indole

7-{2-[7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-1h-indole

C26H26N2 (366.2095876)


   

7-{2-[7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-2,3-dihydro-1h-indole

7-{2-[7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-2,3-dihydro-1h-indole

C26H28N2 (368.2252368)


   

6-{2-[7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-1h-indole

6-{2-[7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-1h-indole

C26H26N2 (366.2095876)


   

pentadecyl (2e)-3-(2-hydroxy-4-methoxyphenyl)prop-2-enoate

pentadecyl (2e)-3-(2-hydroxy-4-methoxyphenyl)prop-2-enoate

C25H40O4 (404.29264400000005)


   

6-{2-[5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl}-1h-indole

6-{2-[5-methyl-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl]ethenyl}-1h-indole

C26H26N2 (366.2095876)


   

{5-[2-(1h-indol-5-yl)ethenyl]-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl}methanol

{5-[2-(1h-indol-5-yl)ethenyl]-7-(2-methylprop-1-en-1-yl)-1h,6h,7h-cyclopenta[f]indol-5-yl}methanol

C26H26N2O (382.2045026)


   

hexadecyl 3-(2-hydroxy-4-methoxyphenyl)prop-2-enoate

hexadecyl 3-(2-hydroxy-4-methoxyphenyl)prop-2-enoate

C26H42O4 (418.30829320000004)


   

5-{2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-1h-indole

5-{2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl}-1h-indole

C26H26N2 (366.2095876)


   

5-[(2r,3r)-3-(3-methylbut-2-en-1-yl)-4-methylideneoxolan-2-yl]-1h-indole

5-[(2r,3r)-3-(3-methylbut-2-en-1-yl)-4-methylideneoxolan-2-yl]-1h-indole

C18H21NO (267.1623056)


   

7-[(1e)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-2,3-dihydro-1h-indole

7-[(1e)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-2,3-dihydro-1h-indole

C26H28N2 (368.2252368)


   

5-[(1e)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

5-[(1e)-2-[(5r,7r)-7-methyl-5-(2-methylprop-1-en-1-yl)-1h,5h,6h-cyclopenta[f]indol-7-yl]ethenyl]-1h-indole

C26H26N2 (366.2095876)