NCBI Taxonomy: 1603838

Strychnos cathayensis (ncbi_taxid: 1603838)

found 17 associated metabolites at species taxonomy rank level.

Ancestor: Strychnos

Child Taxonomies: none taxonomy data.

Campesterol

(1S,2R,5S,10S,11S,14R,15R)-14-[(2R,5R)-5,6-dimethylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol

C28H48O (400.3705)


Campesterol is a phytosterol, meaning it is a 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. -- Wikipedia. Campesterol is a member of phytosterols, a 3beta-sterol, a 3beta-hydroxy-Delta(5)-steroid and a C28-steroid. It has a role as a mouse metabolite. It derives from a hydride of a campestane. Campesterol is a natural product found in Haplophyllum bucharicum, Bugula neritina, and other organisms with data available. Campesterol is a steroid derivative that is the simplest sterol, characterized by the hydroxyl group in position C-3 of the steroid skeleton, and saturated bonds throughout the sterol structure, with the exception of the 5-6 double bond in the B ring. Campesterol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=474-62-4 (retrieved 2024-07-01) (CAS RN: 474-62-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects.

   

4-Aminopropiophenone

4-Aminopropiophenone

C9H11NO (149.0841)


D020011 - Protective Agents > D011837 - Radiation-Protective Agents

   

2-Indolecarboxylic acid

1H-Indole-2-carboxylic acid

C9H7NO2 (161.0477)


2-Indolecarboxylic acid is a strong inhibitor of lipid peroxidation, similar to melatonin and some structurally related indole compounds. Lipid peroxidation with tert-butyl hydroperoxide is a source of free radicals (PMID 12236544). 2-Indolecarboxylic acid is a phenolic components known to exist in Korean ginseng (Koryo Insam Hakhoechi (1996), 20(3), 284-290) and brown rice (Hanguk Nonghwa Hakhoechi (1995), 38(5), 478-83). 2-Indolecarboxylic acid is a strong inhibitor of lipid peroxidation, similar to melatonin and some structurally related indole compounds. COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current[1][2]. Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current[1][2].

   

Butylparaben

Benzoic acid, P-hydroxy-, butyl ester

C11H14O3 (194.0943)


Butylparaben, also known as butyl par asept or tegosept b, belongs to the class of organic compounds known as p-hydroxybenzoic acid alkyl esters. These are aromatic compounds containing a benzoic acid, which is esterified with an alkyl group and para-substituted with a hydroxyl group. Butylparaben displayed the most competitive binding to rat estrogen receptors when tested along with methyl, ethyl, and propylparabens. Butylparaben is a very faint and phenolic tasting compound. Butylparaben is a potentially toxic compound. However, parabens have not been proven to cause breast cancer. It has been used in cosmetic products since the 1940s and in pharmaceutical products since 1924. D010592 - Pharmaceutic Aids > D011310 - Preservatives, Pharmaceutical > D010226 - Parabens Preservative and flavouring agent

   

3-Acetoxyindole

1H-indol-3-yl acetate

C10H9NO2 (175.0633)


   

4'-Aminopropiophenone

1-(4-aminophenyl)propan-1-one

C9H11NO (149.0841)


   

3-Acetylindole

1-(1H-indol-3-yl)ethanone

C10H9NO (159.0684)


IPB_RECORD: 272; CONFIDENCE confident structure

   

3-Methoxysalicylaldehyde

2-Hydroxy-3-methoxybenzaldehyde

C8H8O3 (152.0473)


   

BUTYLPARABEN

butyl 4-hydroxybenzoate

C11H14O3 (194.0943)


D010592 - Pharmaceutic Aids > D011310 - Preservatives, Pharmaceutical > D010226 - Parabens CONFIDENCE standard compound; INTERNAL_ID 839; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4733; ORIGINAL_PRECURSOR_SCAN_NO 4731 CONFIDENCE standard compound; INTERNAL_ID 839; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4751; ORIGINAL_PRECURSOR_SCAN_NO 4749 CONFIDENCE standard compound; INTERNAL_ID 839; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4709; ORIGINAL_PRECURSOR_SCAN_NO 4706 CONFIDENCE standard compound; INTERNAL_ID 839; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4734; ORIGINAL_PRECURSOR_SCAN_NO 4732 CONFIDENCE standard compound; INTERNAL_ID 839; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4776; ORIGINAL_PRECURSOR_SCAN_NO 4775 CONFIDENCE standard compound; INTERNAL_ID 839; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4768; ORIGINAL_PRECURSOR_SCAN_NO 4767 CONFIDENCE standard compound; INTERNAL_ID 2368 CONFIDENCE standard compound; INTERNAL_ID 4234 CONFIDENCE standard compound; INTERNAL_ID 8639 CONFIDENCE standard compound; INTERNAL_ID 4158

   

Indole-2-carboxylic acid

1H-indole-2-carboxylic acid

C9H7NO2 (161.0477)


COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current[1][2]. Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current[1][2].

   

Butoben

Benzoic acid, P-hydroxy-, butyl ester

C11H14O3 (194.0943)


D010592 - Pharmaceutic Aids > D011310 - Preservatives, Pharmaceutical > D010226 - Parabens

   

3-Acetoxyindole

3-Acetoxyindole

C10H9NO2 (175.0633)


   

(4s)-4-tert-butyl-4,5-dihydro-1,3-oxazol-2-ol

(4s)-4-tert-butyl-4,5-dihydro-1,3-oxazol-2-ol

C7H13NO2 (143.0946)


   

3-acetyl indole

3-acetyl indole

C10H9NO (159.0684)


   

5-ethenyl-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-1-one

5-ethenyl-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-1-one

C10H12O3 (180.0786)


   

4-tert-butyl-4,5-dihydro-1,3-oxazol-2-ol

4-tert-butyl-4,5-dihydro-1,3-oxazol-2-ol

C7H13NO2 (143.0946)


   

(4as,5r)-5-ethenyl-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-1-one

(4as,5r)-5-ethenyl-3h,4h,4ah,5h,6h-pyrano[3,4-c]pyran-1-one

C10H12O3 (180.0786)