NCBI Taxonomy: 78793
Liparis (ncbi_taxid: 78793)
found 37 associated metabolites at genus taxonomy rank level.
Ancestor: Malaxidinae
Child Taxonomies: Liparis mai, Liparis laxa, Liparis tsii, Liparis sula, Liparis nigra, Liparis somae, Liparis mannii, Liparis nutans, Liparis barbata, Liparis rhombea, Liparis koreana, Liparis krameri, Liparis montana, Liparis distans, Liparis sasakii, Liparis luteola, Liparis reflexa, Liparis nervosa, Liparis rheedei, Liparis odorata, Liparis bowkeri, Liparis deflexa, Liparis glossula, Liparis maingayi, Liparis truncata, Liparis gigantea, Liparis rostrata, Liparis disticha, Liparis balansae, Liparis japonica, Liparis loeselii, Liparis kumokiri, Liparis layardii, Liparis pauliana, Liparis vivipara, Liparis pingtaoi, Liparis assamica, Liparis bistriata, Liparis elliptica, Liparis yongnoana, Liparis napoensis, Liparis petiolata, Liparis makinoana, Liparis suzumushi, Liparis bracteata, Liparis cespitosa, Liparis chalandei, Liparis clypeolum, Liparis formosana, Liparis anopheles, Liparis latifolia, Liparis nugentiae, Liparis pandurata, Liparis delicatula, Liparis latilabris, Liparis resupinata, Liparis hostifolia, Liparis auriculata, Liparis ferruginea, Liparis cordifolia, Liparis habenarina, Liparis hawaiensis, Liparis terrestris, Liparis truncicola, Liparis liliifolia, Liparis parviflora, Liparis cathcartii, Liparis lindeniana, Liparis fissipetala, Liparis pterosepala, Liparis mengziensis, Liparis derchiensis, Liparis sparsiflora, Liparis viridiflora, Liparis brunnescens, Liparis funingensis, Liparis crispifolia, Liparis bootanensis, Liparis macrosepala, Liparis wenshanensis, Liparis aureolabella, Liparis nanlingensis, Liparis fujisanensis, Liparis guangxiensis, Liparis bautingensis, Liparis brachyglottis, Liparis longiracemosa, Liparis koreojaponica, Liparis pingxiangensis, Liparis sootenzanensis, Liparis stricklandiana, Liparis purpureoviridis, Liparis purpureovittata, Liparis meihuashanensis, Liparis cf. japonica L26, Liparis cf. distans LipV, Liparis bingzhongluoensis, Liparis aff. elegans MO-2021, unclassified Liparis (in: monocots)
6-beta-D-Glucopyranosyl-8-beta-D-ribopyranosylapigenin
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]-8-(3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)-4H-chromen-4-one is a member of flavonoids and a C-glycosyl compound. 5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one is a natural product found in Cymbidium kanran, Acanthus, and other organisms with data available. 6-beta-D-Glucopyranosyl-8-beta-D-ribopyranosylapigenin is found in herbs and spices. 6-beta-D-Glucopyranosyl-8-beta-D-ribopyranosylapigenin is a constituent of Passiflora incarnata (maypops). Constituent of Passiflora incarnata (maypops). Apigenin 6-C-glucoside 8-C-riboside is found in herbs and spices. Neoschaftoside is a flavone C-glycoside that is apigenin attached to a beta-D-glucopyranosyl and a beta-L-arabinopyranosyl residues at positions 6 and 8 respectively via C-glycosidic linkage. It has a role as a plant metabolite. It is a flavone C-glycoside and a dihydroxyflavone. It is functionally related to an apigenin. Neoschaftoside is a natural product found in Radula complanata, Artemisia judaica, and other organisms with data available. Schaftoside is a flavonoid found in a variety of Chinese herbal medicines, such as Eleusine indica. Schaftoside inhibits the expression of TLR4 and Myd88. Schaftoside also decreases Drp1 expression and phosphorylation, and reduces mitochondrial fission[1]. Schaftoside is a flavonoid found in a variety of Chinese herbal medicines, such as Eleusine indica. Schaftoside inhibits the expression of TLR4 and Myd88. Schaftoside also decreases Drp1 expression and phosphorylation, and reduces mitochondrial fission[1]. Schaftoside is a flavonoid found in a variety of Chinese herbal medicines, such as Eleusine indica. Schaftoside inhibits the expression of TLR4 and Myd88. Schaftoside also decreases Drp1 expression and phosphorylation, and reduces mitochondrial fission[1].
Guanidine
Guanidine apparently acts by enhancing the release of acetylcholine following a nerve impulse. It also appears to slow the rates of depolarization and repolarization of muscle cell membranes.; Guanidine is a crystalline compound of strong alkalinity formed by the oxidation of guanine. It is used in the manufacture of plastics and explosives. It is found in urine as a normal product of protein metabolism. The molecule was first synthesized in 1861 by the oxidative degradation of an aromatic natural product, guanine, isolated from Peruvian guano. Despite the provocative simplicity of the molecule, the crystal structure was first described 148 years later.; Guanidine is a polyamine that can function as a strong organic base existing primarily as guanidium ions at physiological pH. With a pKa of 12.5, guanidine is protonated, with a charge of +1 in physiological conditions. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed). Guanidine is a crystalline compound of strong alkalinity formed by the oxidation of guanine. It is used in the manufacture of plastics and explosives. -- Wikipedia; Guanidines are a group of organic compounds sharing a common functional group with the general structure (R1R2N)(R3R4N)C=N-R5. The central bond within this group is that of an imine; the other recognizable motif within this group is an aminal. Examples of guanidines are arginine, triazabicyclodecene and saxitoxin. other derivatives could include guanidine hydroxide, the active ingredient in some non-lye relaxers. Guanidinium salts are well known for their denaturing action on proteins. Guanidinium chloride is one of the most effective denaturants. In 6 M GndHCl all proteins with an ordered structure lose their structure, and most of them become randomly coiled, that is, they do not contain any residual structure. Guanidine is a polyamine that can function as a strong organic base existing primarily as guanidium ions at physiological pH. With a pKa of 12.5, guanidine is protonated, with a charge of +1 in physiological conditions. It is found in the urine as a normal product of protein metabolism. It has been identified as a uremic toxin according to the European Uremic Toxin Working Group (PMID: 22626821). Guanidine is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed). Guanidine is a crystalline compound of strong alkalinity formed by the oxidation of guanine. It is used in the manufacture of plastics and explosives. -- Wikipedia.
Schaftoside
Apigenin 6-c-glucoside 8-c-riboside is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Apigenin 6-c-glucoside 8-c-riboside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Apigenin 6-c-glucoside 8-c-riboside can be found in herbs and spices, which makes apigenin 6-c-glucoside 8-c-riboside a potential biomarker for the consumption of this food product. Schaftoside is a flavonoid found in a variety of Chinese herbal medicines, such as Eleusine indica. Schaftoside inhibits the expression of TLR4 and Myd88. Schaftoside also decreases Drp1 expression and phosphorylation, and reduces mitochondrial fission[1]. Schaftoside is a flavonoid found in a variety of Chinese herbal medicines, such as Eleusine indica. Schaftoside inhibits the expression of TLR4 and Myd88. Schaftoside also decreases Drp1 expression and phosphorylation, and reduces mitochondrial fission[1]. Schaftoside is a flavonoid found in a variety of Chinese herbal medicines, such as Eleusine indica. Schaftoside inhibits the expression of TLR4 and Myd88. Schaftoside also decreases Drp1 expression and phosphorylation, and reduces mitochondrial fission[1].
Nudol
2,7-Phenanthrenediol, 3,4-dimethoxy- is a natural product found in Pinalia spicata, Bulbophyllum vaginatum, and other organisms with data available.
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one
(2s,3r,4s,5s,6r)-3-(4-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-3,5-bis(3-methylbut-2-en-1-yl)benzoyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl 4-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-3,5-bis(3-methylbut-2-en-1-yl)benzoate
4-hydroxy-3,5-bis(3-hydroxy-3-methylbutyl)benzoic acid
3,4,5-trihydroxy-6-methyloxan-2-yl 4-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,5-bis(3-methylbut-2-en-1-yl)benzoate
(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl 4-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-3,5-bis(3-methylbut-2-en-1-yl)benzoate
4-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,5-bis(3-methylbut-2-en-1-yl)benzoic acid
4-{[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-3,5-bis(3-methylbut-2-en-1-yl)benzoic acid
4-hydroxy-3,5-bis(2-hydroxy-3-methylbut-3-en-1-yl)benzoic acid
(7a-methyl-hexahydropyrrolizin-1-yl)methyl 4-hydroxy-3-methoxy-5-(3-methylbut-2-en-1-yl)benzoate
C22H31NO4 (373.22529660000004)
3-(4-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,5-bis(3-methylbut-2-en-1-yl)benzoyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl 4-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,5-bis(3-methylbut-2-en-1-yl)benzoate
hexahydro-1h-pyrrolizin-1-ylmethyl 3-methoxy-5-(3-methylbut-2-en-1-yl)-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzoate
8-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-2,2-dimethylchromene-6-carboxylic acid
[(1s,7ar)-7a-methyl-hexahydropyrrolizin-1-yl]methyl 4-hydroxy-3-methoxy-5-(3-methylbut-2-en-1-yl)benzoate
C22H31NO4 (373.22529660000004)