NCBI Taxonomy: 3828

Crotalaria (ncbi_taxid: 3828)

found 64 associated metabolites at genus taxonomy rank level.

Ancestor: Crotalarieae

Child Taxonomies: Crotalaria incana, Crotalaria juncea, Crotalaria pallida, Crotalaria nana, Crotalaria dura, Crotalaria podocarpa, Crotalaria aurea, Crotalaria hirta, Crotalaria grata, Crotalaria annua, Crotalaria alata, Crotalaria laeta, Crotalaria recta, Crotalaria dubia, Crotalaria ballyi, Crotalaria eximia, Crotalaria scabra, Crotalaria grevei, Crotalaria pumila, Crotalaria balboi, Crotalaria fallax, Crotalaria kanaii, Crotalaria adolfi, Crotalaria amoena, Crotalaria pudica, Crotalaria barkae, Crotalaria comosa, Crotalaria glauca, Crotalaria retusa, Crotalaria vialis, Crotalaria pilosa, Crotalaria dumosa, Crotalaria excisa, Crotalaria burhia, Crotalaria lunata, Crotalaria kirkii, Crotalaria kurtii, Crotalaria albida, Crotalaria micans, Crotalaria tanety, Crotalaria kurzii, Crotalaria mairei, Crotalaria nitens, Crotalaria reptans, Crotalaria shanica, Crotalaria spartea, Crotalaria stolzii, Crotalaria eremaea, Crotalaria bifaria, Crotalaria clarkei, Crotalaria filipes, Crotalaria bosseri, Crotalaria caudata, Crotalaria coursii, Crotalaria oocarpa, Crotalaria distans, Crotalaria humilis, Crotalaria paulina, Crotalaria confusa, Crotalaria florida, Crotalaria montana, Crotalaria notonii, Crotalaria doniana, Crotalaria harleyi, Crotalaria pusilla, Crotalaria persica, Crotalaria hirsuta, Crotalaria vestita, Crotalaria inflexa, Crotalaria intonsa, Crotalaria pellita, Crotalaria lukomae, Crotalaria anomala, Crotalaria aiantha, Crotalaria pygmaea, Crotalaria quarrei, Crotalaria boehmii, Crotalaria barbata, Crotalaria friesii, Crotalaria similis, Crotalaria burttii, Crotalaria rosenii, Crotalaria purshii, Crotalaria dinteri, Crotalaria goetzei, Crotalaria saharae, Crotalaria spinosa, Crotalaria miranda, Crotalaria fysonii, Crotalaria obscura, Crotalaria obtecta, Crotalaria parvula, Crotalaria pulchra, Crotalaria arushae, Crotalaria walkeri, Crotalaria dedzana, Crotalaria occulta, Crotalaria irwinii, Crotalaria otoptera, Crotalaria doidgeae, Crotalaria rufipila, Crotalaria speciosa, Crotalaria varicosa, Crotalaria assamica, Crotalaria bernieri, Crotalaria heyneana, Crotalaria balansae, Crotalaria carsonii, Crotalaria crispata, Crotalaria saltiana, Crotalaria congesta, Crotalaria cornetii, Crotalaria martiana, Crotalaria diminuta, Crotalaria exilipes, Crotalaria purdiana, Crotalaria lunulata, Crotalaria thebaica, Crotalaria lejoloba, Crotalaria aculeata, Crotalaria arenaria, Crotalaria calycina, Crotalaria argyraea, Crotalaria boranica, Crotalaria sessilis, Crotalaria gazensis, Crotalaria burkeana, Crotalaria subtilis, Crotalaria colorata, Crotalaria lebrunii, Crotalaria vatkeana, Crotalaria rogersii, Crotalaria duboisii, Crotalaria lotoides, Crotalaria velutina, Crotalaria ephemera, Crotalaria angulata, Crotalaria hemsleyi, Crotalaria impressa, Crotalaria capensis, Crotalaria iringana, Crotalaria mauensis, Crotalaria meyerana, Crotalaria longipes, Crotalaria perrieri, Crotalaria concinna, Crotalaria humifusa, Crotalaria khasiana, Crotalaria miottoae, Crotalaria mortonii, Crotalaria capuronii, Crotalaria deflersii, Crotalaria rhodesiae, Crotalaria shirensis, Crotalaria uliginosa, Crotalaria vanmeelii, Crotalaria variegata, Crotalaria filifolia, Crotalaria alexandri, Crotalaria virgulata, Crotalaria epunctata, Crotalaria axillaris, Crotalaria lutescens, Crotalaria prostrata, Crotalaria greenwayi, Crotalaria triquetra, Crotalaria natalitia, Crotalaria orixensis, Crotalaria steudneri, Crotalaria vallicola, Crotalaria avonensis, Crotalaria assurgens, Crotalaria callensii, Crotalaria ebenoides, Crotalaria flavicoma, Crotalaria lotifolia, Crotalaria dasyclada, Crotalaria germainii, Crotalaria stipitata, Crotalaria nyikensis, Crotalaria pearsonii, Crotalaria peschiana, Crotalaria praetexta, Crotalaria becquetii, Crotalaria aridicola, Crotalaria ringoetii, Crotalaria bongensis, Crotalaria goreensis, Crotalaria chinensis, Crotalaria brevidens, Crotalaria hilariana, Crotalaria chirindae, Crotalaria cistoides, Crotalaria longidens, Crotalaria petitiana, Crotalaria cuspidata, Crotalaria ononoides, Crotalaria polhillii, Crotalaria decaryana, Crotalaria vitellina, Crotalaria smithiana, Crotalaria tweediana, Crotalaria uncinella, Crotalaria eremicola, Crotalaria gillettii, Crotalaria globifera, Crotalaria verrucosa, Crotalaria inopinata, Crotalaria keniensis, Crotalaria laxiflora, Crotalaria monteiroi, Crotalaria hebecarpa, Crotalaria muenzneri, Crotalaria laevigata, Crotalaria nigricans, Crotalaria adamsonii, Crotalaria tetragona, Crotalaria pisicarpa, Crotalaria plowdenii, Crotalaria wightiana, Crotalaria poissonii, Crotalaria bracteata, Crotalaria teixeirae, Crotalaria vasculosa, Crotalaria linifolia, Crotalaria mollicula, Crotalaria sagittalis, Crotalaria schiedeana, Crotalaria strigulosa, Crotalaria polyphylla, Crotalaria abbreviata, Crotalaria cephalotes, Crotalaria durandiana, Crotalaria emirnensis, Crotalaria griquensis, Crotalaria orthoclada, Crotalaria breviflora, Crotalaria abscondita, Crotalaria ferruginea, Crotalaria deightonii, Crotalaria prolongata, Crotalaria rzedowskii, Crotalaria paniculata, Crotalaria johnstonii, Crotalaria natalensis, Crotalaria albicaulis, Crotalaria allophylla, Crotalaria polysperma, Crotalaria acicularis, Crotalaria pterocalyx, Crotalaria atrorubens, Crotalaria bequaertii, Crotalaria rhizoclada, Crotalaria bogdaniana, Crotalaria glaucoides, Crotalaria rufocaulis, Crotalaria berteroana, Crotalaria lanceolata, Crotalaria somalensis, Crotalaria ochroleuca, Crotalaria goiasensis, Crotalaria capillipes, Crotalaria uguenensis, Crotalaria ukambensis, Crotalaria monophylla, Crotalaria multiflora, Crotalaria cylindrica, Crotalaria orientalis, Crotalaria damarensis, Crotalaria stipularia, Crotalaria emarginata, Crotalaria filicaulis, Crotalaria gamwelliae, Crotalaria grahamiana, Crotalaria madurensis, Crotalaria mysorensis, Crotalaria heidmannii, Crotalaria tweedieana, Crotalaria leandriana, Crotalaria lotiformis, Crotalaria macrocarpa, Crotalaria microcarpa, Crotalaria lachnosema, Crotalaria macrocalyx, Crotalaria agatiflora, Crotalaria mudugensis, Crotalaria beddomeana, Crotalaria trichotoma, Crotalaria phylloloba, Crotalaria cytisoides, Crotalaria aegyptiaca, Crotalaria bahiaensis, Crotalaria claussenii, Crotalaria filiformis, Crotalaria ibityensis, Crotalaria lasiocarpa, Crotalaria leprieurii, Crotalaria mitchellii, Crotalaria vespertilio, Crotalaria yunnanensis, Crotalaria maypurensis, Crotalaria androyensis, Crotalaria ankaratrana, Crotalaria diosmifolia, Crotalaria emarginella, Crotalaria salicifolia, Crotalaria graminicola, Crotalaria luondeensis, Crotalaria spectabilis, Crotalaria virgultaris, Crotalaria pleiophylla, Crotalaria cajanifolia, Crotalaria cobalticola, Crotalaria cyanoxantha, Crotalaria quartiniana, Crotalaria quercetorum, Crotalaria griseofusca, Crotalaria ramosissima, Crotalaria inyangensis, Crotalaria kapiriensis, Crotalaria xanthoclada, Crotalaria kerkvoordei, Crotalaria kwengeensis, Crotalaria ledermannii, Crotalaria melanocarpa, Crotalaria phillipsiae, Crotalaria barnabassii, Crotalaria lathyroides, Crotalaria sparsifolia, Crotalaria perrottetii, Crotalaria grandiflora, Crotalaria stuhlmannii, Crotalaria holosericea, Crotalaria teretifolia, Crotalaria lachnophora, Crotalaria cleomifolia, Crotalaria umbellifera, Crotalaria deserticola, Crotalaria ulbrichiana, Crotalaria humbertiana, Crotalaria karagwensis, Crotalaria kipandensis, Crotalaria laburnoides, Crotalaria massaiensis, Crotalaria melanocalyx, Crotalaria mesopontica, Crotalaria microphylla, Crotalaria oligosperma, Crotalaria pilosiflora, Crotalaria platysepala, Crotalaria boliviensis, Crotalaria prittwitzii, Crotalaria sericifolia, Crotalaria spartioides, Crotalaria medicaginea, Crotalaria lepidissima, Crotalaria mildbraedii, Crotalaria brachycarpa, Crotalaria sandoorensis, Crotalaria subdecurrens, Crotalaria trifoliolata, Crotalaria quinquefolia, Crotalaria fiherenensis, Crotalaria mahafalensis, Crotalaria rotundifolia, Crotalaria scassellatii, unclassified Crotalaria, Crotalaria chrysotricha, Crotalaria lebeckioides, Crotalaria anthyllopsis, Crotalaria benadirensis, Crotalaria rhynchocarpa, Crotalaria serengetiana, Crotalaria hyssopifolia, Crotalaria stenorhampha, Crotalaria camptosepala, Crotalaria senegalensis, Crotalaria sphaerocarpa, Crotalaria chrysochlora, Crotalaria comanestiana, Crotalaria sessiliflora, Crotalaria laburnifolia, Crotalaria dissitiflora, Crotalaria unifoliolata, Crotalaria fascicularis, Crotalaria goodiiformis, Crotalaria cunninghamii, Crotalaria pycnostachya, Crotalaria malindiensis, Crotalaria microthamnus, Crotalaria evolvuloides, Crotalaria brevicornuta, Crotalaria nayaritensis, Crotalaria pallidicaulis, Crotalaria trifoliastrum, Crotalaria cornu-ammonis, Crotalaria longirostrata, Crotalaria afrocentralis, Crotalaria phyllostachya, Crotalaria cylindrocarpa, Crotalaria tenuirostrata, Crotalaria vandenbrandii, Crotalaria craspedocarpa, Crotalaria willdenowiana, Crotalaria distantiflora, Crotalaria flavicarinata, Crotalaria incrassifolia, Crotalaria involutifolia, Crotalaria passerinoides, Crotalaria semperflorens, Crotalaria shevaroyensis, Crotalaria subperfoliata, Crotalaria bupleurifolia, Crotalaria meghalayensis, Crotalaria kurisumalayana, Crotalaria adenocarpoides, Crotalaria dewildemaniana, Crotalaria lukwangulensis, Crotalaria argyrolobioides, Crotalaria lachnocarpoides, Crotalaria grandibracteata, Crotalaria cylindrostachys, Crotalaria grandistipulata, Crotalaria axillifloroides, Crotalaria pseudotenuirama, Crotalaria tenuipedicellata, Crotalaria brevipedunculata, Crotalaria linearifoliolata, Crotalaria novae-hollandiae, Crotalaria pseudodiloloensis, Crotalaria magaliesbergensis, Crotalaria argenteotomentosa, Crotalaria chaco-serranensis, Crotalaria cf. agatiflora QZ-2022

Stearic acid

1-Heptadecanecarboxylic acid

C18H36O2 (284.2715156)


Stearic acid, also known as stearate or N-octadecanoic acid, is a member of the class of compounds known as long-chain fatty acids. Long-chain fatty acids are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. Thus, stearic acid is considered to be a fatty acid lipid molecule. Stearic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Stearic acid can be synthesized from octadecane. Stearic acid is also a parent compound for other transformation products, including but not limited to, 3-oxooctadecanoic acid, (9S,10S)-10-hydroxy-9-(phosphonooxy)octadecanoic acid, and 16-methyloctadecanoic acid. Stearic acid can be found in a number of food items such as green bell pepper, common oregano, ucuhuba, and babassu palm, which makes stearic acid a potential biomarker for the consumption of these food products. Stearic acid can be found primarily in most biofluids, including urine, feces, cerebrospinal fluid (CSF), and sweat, as well as throughout most human tissues. Stearic acid exists in all living species, ranging from bacteria to humans. In humans, stearic acid is involved in the plasmalogen synthesis. Stearic acid is also involved in mitochondrial beta-oxidation of long chain saturated fatty acids, which is a metabolic disorder. Moreover, stearic acid is found to be associated with schizophrenia. Stearic acid is a non-carcinogenic (not listed by IARC) potentially toxic compound. Stearic acid ( STEER-ik, stee-ARR-ik) is a saturated fatty acid with an 18-carbon chain and has the IUPAC name octadecanoic acid. It is a waxy solid and its chemical formula is C17H35CO2H. Its name comes from the Greek word στέαρ "stéar", which means tallow. The salts and esters of stearic acid are called stearates. As its ester, stearic acid is one of the most common saturated fatty acids found in nature following palmitic acid. The triglyceride derived from three molecules of stearic acid is called stearin . Stearic acid, also known as octadecanoic acid or C18:0, belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. Stearic acid (its ester is called stearate) is a saturated fatty acid that has 18 carbons and is therefore a very hydrophobic molecule that is practically insoluble in water. It exists as a waxy solid. In terms of its biosynthesis, stearic acid is produced from carbohydrates via the fatty acid synthesis machinery wherein acetyl-CoA contributes two-carbon building blocks, up to the 16-carbon palmitate, via the enzyme complex fatty acid synthase (FA synthase), at which point a fatty acid elongase is needed to further lengthen it. After synthesis, there are a variety of reactions it may undergo, including desaturation to oleate via stearoyl-CoA desaturase (PMID: 16477801). Stearic acid is found in all living organisms ranging from bacteria to plants to animals. It is one of the useful types of saturated fatty acids that comes from many animal and vegetable fats and oils. For example, it is a component of cocoa butter and shea butter. It is used as a food additive, in cleaning and personal care products, and in lubricants. Its name comes from the Greek word stear, which means ‚Äòtallow‚Äô or ‚Äòhard fat‚Äô. Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils. Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils.

   

Monocrotaline

5,6-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

C16H23NO6 (325.1525298)


Hepatotoxin. Causative agent of much seneciosis, e.g. accidental poisoning by S. by weed residues in bread, and characterised by venoocculosive disease Hepatotoxin. Causative agent of much seneciosis, e.g. accidental poisoning by S. by weed residues in bread, and characterised by venoocculosive diseas CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2249 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 131 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 121 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 151 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 141 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 111 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 161 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 171 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 101 Monocrotaline is an 11-membered macrocyclic pyrrolizidine alkaloid. Monocrotaline inhibits OCT-1 and OCT-2 with IC50s of 36.8 μM and 1.8 mM, respectively. Monocrotaline has antitumor activity and is cytotoxic to hepatocellular carcinoma cells. Monocrotaline is used to induce a model of pulmonary hypertension in rodents. [2][6][8]. Monocrotaline is an 11-membered macrocyclic pyrrolizidine alkaloid. Monocrotaline inhibits OCT-1 and OCT-2 with IC50s of 36.8 μM and 1.8 mM, respectively. Monocrotaline has antitumor activity and is cytotoxic to hepatocellular carcinoma cells. Monocrotaline is used to induce a model of pulmonary hypertension in rodents. [2][6][8].

   

Iridin

5-hydroxy-3-(3-hydroxy-4,5-dimethoxyphenyl)-6-methoxy-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C24H26O13 (522.1373346)


Iridin is a glycosyloxyisoflavone that is irigenin substituted by a beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage. It has a role as a plant metabolite. It is a hydroxyisoflavone, a monosaccharide derivative, a member of 4-methoxyisoflavones and a 7-hydroxyisoflavones 7-O-beta-D-glucoside. It is functionally related to an irigenin. Iridin is a natural product found in Iris milesii, Iris tectorum, and other organisms with data available. See also: Iris versicolor root (part of). A glycosyloxyisoflavone that is irigenin substituted by a beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage. Iridin is an isoflavone isolated from Iris milesii[1]. Iridin is an isoflavone isolated from Iris milesii[1].

   

2'-Hydroxygenistein

3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one, 9CI

C15H10O6 (286.047736)


Isolated from Cajanus cajan (pigeon pea), Dolichos biflorus (papadi), Lablab niger (hyacinth bean), Phaseolus vulgaris (kidney bean) and Phaseolus coccineus (scarlet runner bean). 2-Hydroxygenistein is found in many foods, some of which are pulses, walnut, saskatoon berry, and garden tomato (variety). 2-Hydroxygenistein is found in adzuki bean. 2-Hydroxygenistein is isolated from Cajanus cajan (pigeon pea), Dolichos biflorus (papadi), Lablab niger (hyacinth bean), Phaseolus vulgaris (kidney bean) and Phaseolus coccineus (scarlet runner bean).

   

Cajanin

4H-1-Benzopyran-4-one, 3-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-

C16H12O6 (300.06338519999997)


Cajanin is a member of 7-methoxyisoflavones. It has a role as a metabolite. Cajanin is a natural product found in Crotalaria lachnophora, Dalbergia parviflora, and other organisms with data available. Isolated from Cajanus cajan (pigeon pea), Canavalia ensiformis (jack bean). Cajanin is found in pigeon pea, coffee and coffee products, and pulses. Cajanin is found in coffee and coffee products. Cajanin is isolated from Cajanus cajan (pigeon pea), Canavalia ensiformis (jack bean A natural product found in Crotalaria lachnophora.

   

Quercimeritrin

Quercetin 7-O-beta-D-glucoside

C21H20O12 (464.09547200000003)


Quercimeritrin, isolated from the leaves of Ixeridium dentatum, exhibits significant amylase activity[1]. Quercimeritrin, isolated from the leaves of Ixeridium dentatum, exhibits significant amylase activity[1].

   

Apigenin 7-apiosyl-glucoside

7-{[(2S,3R,4S,5S,6R)-6-({[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-5-hydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C26H28O14 (564.1478988)


Apigenin 7-apiosyl-glucoside is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Apigenin 7-apiosyl-glucoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Apigenin 7-apiosyl-glucoside can be found in german camomile, parsley, roman camomile, and wild celery, which makes apigenin 7-apiosyl-glucoside a potential biomarker for the consumption of these food products.

   

Monocrotaline

2H-(1,6)DIOXACYCLOUNDECINO(2,3,4-GH)PYRROLIZINE-2,6(3H)-DIONE, 4,5,8,10,12,13,13A,13B-OCTAHYDRO-4,5-DIHYDROXY-3,4,5-TRIMETHYL-, (3R-(3R*,4R*,5R*,13AR*,13BR*))-

C16H23NO6 (325.1525298)


Monocrotaline is a pyrrolizidine alkaloid. Monocrotaline is a natural product found in Crotalaria novae-hollandiae, Crotalaria recta, and other organisms with data available. A pyrrolizidine alkaloid and a toxic plant constituent that poisons livestock and humans through the ingestion of contaminated grains and other foods. The alkaloid causes pulmonary artery hypertension, right ventricular hypertrophy, and pathological changes in the pulmonary vasculature. Significant attenuation of the cardiopulmonary changes are noted after oral magnesium treatment. Origin: Plant; SubCategory_DNP: Alkaloids derived from ornithine, Pyrrolizidine alkaloids relative retention time with respect to 9-anthracene Carboxylic Acid is 0.154 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.142 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.145 Monocrotaline is an 11-membered macrocyclic pyrrolizidine alkaloid. Monocrotaline inhibits OCT-1 and OCT-2 with IC50s of 36.8 μM and 1.8 mM, respectively. Monocrotaline has antitumor activity and is cytotoxic to hepatocellular carcinoma cells. Monocrotaline is used to induce a model of pulmonary hypertension in rodents. [2][6][8]. Monocrotaline is an 11-membered macrocyclic pyrrolizidine alkaloid. Monocrotaline inhibits OCT-1 and OCT-2 with IC50s of 36.8 μM and 1.8 mM, respectively. Monocrotaline has antitumor activity and is cytotoxic to hepatocellular carcinoma cells. Monocrotaline is used to induce a model of pulmonary hypertension in rodents. [2][6][8].

   

Quercimeritrin

2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C21H20O12 (464.09547200000003)


Quercetin 7-O-beta-D-glucoside is a quercetin O-glucoside in which a glucosyl residue is attached at position 7 of quercetin via a beta-glycosidic linkage. It has a role as an antioxidant and a metabolite. It is a beta-D-glucoside, a monosaccharide derivative, a member of flavonols, a tetrahydroxyflavone and a quercetin O-glucoside. Quercimeritrin is a natural product found in Salix atrocinerea, Dendroviguiera sphaerocephala, and other organisms with data available. See also: Chamomile (part of). Quercimeritrin, isolated from the leaves of Ixeridium dentatum, exhibits significant amylase activity[1]. Quercimeritrin, isolated from the leaves of Ixeridium dentatum, exhibits significant amylase activity[1].

   

Crotaramin

1- (5-Hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl) -3- (4-methoxyphenyl) -1-propanone

C21H22O4 (338.1518012)


   

Cajanin

5,2,4-Trihydroxy-7-methoxyisoflavone

C16H12O6 (300.06338519999997)


   

2'-Hydroxygenistein

3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one, 9CI

C15H10O6 (286.047736)


2-hydroxygenistein is a hydroxyisoflavone that is genistein substituted by an additional hydroxy group at position 2. It has been isolated from Crotalaria lachnophora. It has a role as a plant metabolite. It is functionally related to a genistein. It is a conjugate acid of a 2-hydroxygenistein(1-). 2-Hydroxygenistein is a natural product found in Crotalaria lachnophora, Vigna radiata, and other organisms with data available. Isolated from Cajanus cajan (pigeon pea), Dolichos biflorus (papadi), Lablab niger (hyacinth bean), Phaseolus vulgaris (kidney bean) and Phaseolus coccineus (scarlet runner bean). 2-Hydroxygenistein is found in many foods, some of which are pulses, walnut, saskatoon berry, and garden tomato (variety). 2-Hydroxygenistein is found in adzuki bean. 2-Hydroxygenistein is isolated from Cajanus cajan (pigeon pea), Dolichos biflorus (papadi), Lablab niger (hyacinth bean), Phaseolus vulgaris (kidney bean) and Phaseolus coccineus (scarlet runner bean). A hydroxyisoflavone that is genistein substituted by an additional hydroxy group at position 2. It has been isolated from Crotalaria lachnophora.

   

stearic acid

stearic acid

C18H36O2 (284.2715156)


Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils. Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils.

   

Octadecanoic acid

Octadecanoic acid

C18H36O2 (284.2715156)


A C18 straight-chain saturated fatty acid component of many animal and vegetable lipids. As well as in the diet, it is used in hardening soaps, softening plastics and in making cosmetics, candles and plastics.

   

linoleic

9,12-Octadecadienoic acid, (9E,12E)-

C18H32O2 (280.2402172)


Linolelaidic acid (Linoelaidic acid), an omega-6 trans fatty acid, acts as a source of energy. Linolelaidic acid is an essential nutrient, adding in enteral, parenteral, and infant formulas. Linolelaidic acid can be used for heart diseases research[1]. Linolelaidic acid (Linoelaidic acid), an omega-6 trans fatty acid, acts as a source of energy. Linolelaidic acid is an essential nutrient, adding in enteral, parenteral, and infant formulas. Linolelaidic acid can be used for heart diseases research[1].

   

Apigenin 7-apiosyl-glucoside

7-{[(2S,3R,4S,5S,6R)-6-({[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-5-hydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C26H28O14 (564.1478988)


Apigenin 7-apiosyl-glucoside is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Apigenin 7-apiosyl-glucoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Apigenin 7-apiosyl-glucoside can be found in german camomile, parsley, roman camomile, and wild celery, which makes apigenin 7-apiosyl-glucoside a potential biomarker for the consumption of these food products.

   

9-hydroxy-5,8,9-trimethyl-2,7,11-trioxa-16-azatetracyclo[11.5.1.0⁴,⁸.0¹⁶,¹⁹]nonadec-13-ene-3,6,10-trione

9-hydroxy-5,8,9-trimethyl-2,7,11-trioxa-16-azatetracyclo[11.5.1.0⁴,⁸.0¹⁶,¹⁹]nonadec-13-ene-3,6,10-trione

C18H23NO7 (365.1474448)


   

(1r,4s,5r,6s,10r,16r)-5,6-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadecane-3,7-dione

(1r,4s,5r,6s,10r,16r)-5,6-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadecane-3,7-dione

C16H25NO6 (327.168179)


   

7-{[(2s,3r,4s,5s,6r)-6-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-5-hydroxy-2-(4-methoxyphenyl)chromen-4-one

7-{[(2s,3r,4s,5s,6r)-6-({[(2r,3r,4r)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-5-hydroxy-2-(4-methoxyphenyl)chromen-4-one

C27H30O14 (578.163548)


   

(1'r,2s,3r,6'r,7'r,17'r)-7'-hydroxy-3,6',7'-trimethyl-2',9'-dioxa-14'-azaspiro[oxirane-2,4'-tricyclo[9.5.1.0¹⁴,¹⁷]heptadecan]-11'-ene-3',8'-dione

(1'r,2s,3r,6'r,7'r,17'r)-7'-hydroxy-3,6',7'-trimethyl-2',9'-dioxa-14'-azaspiro[oxirane-2,4'-tricyclo[9.5.1.0¹⁴,¹⁷]heptadecan]-11'-ene-3',8'-dione

C18H25NO6 (351.168179)


   

(1r,5s,16s)-5-hydroxy-5-methyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

(1r,5s,16s)-5-hydroxy-5-methyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

C14H19NO5 (281.1263164)


   

(1r,4r,5r,6r,16r)-5,6-dihydroxy-6-(hydroxymethyl)-4-isopropyl-5-methyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

(1r,4r,5r,6r,16r)-5,6-dihydroxy-6-(hydroxymethyl)-4-isopropyl-5-methyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

C18H27NO7 (369.1787432)


   

3-[5-(hydroxymethyl)-5-methyl-2-oxofuran-3-yl]-2-methylpropanoic acid

3-[5-(hydroxymethyl)-5-methyl-2-oxofuran-3-yl]-2-methylpropanoic acid

C10H14O5 (214.08411940000002)


   

(1s,4e,6s,7r,16r,17r)-4-ethylidene-7,16-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

(1s,4e,6s,7r,16r,17r)-4-ethylidene-7,16-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

C18H25NO6 (351.168179)


   

(1r,4r,7s,11z,18s)-4-ethyl-7,14,18-trimethyl-2,6,9-trioxa-14-azatricyclo[9.5.1.1⁴,⁷]octadec-11-ene-3,5,8,17-tetrone

(1r,4r,7s,11z,18s)-4-ethyl-7,14,18-trimethyl-2,6,9-trioxa-14-azatricyclo[9.5.1.1⁴,⁷]octadec-11-ene-3,5,8,17-tetrone

C19H25NO7 (379.163094)


   

1-methyl-hexahydro-1h-pyrrolizine

1-methyl-hexahydro-1h-pyrrolizine

C8H15N (125.120443)


   
   

(1r,5r,6s,16r)-6-hydroxy-5,6-dimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

(1r,5r,6s,16r)-6-hydroxy-5,6-dimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

C15H21NO5 (295.1419656)


   

(1r,4e,6s,7r,17s)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

(1r,4e,6s,7r,17s)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

C18H25NO5 (335.173264)


   

(1r,4r,4ar,7s,7as)-1-{[(1r,3as,3bs,7r,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-4,7-dimethyl-hexahydro-1h-cyclopenta[c]pyran-3-one

(1r,4r,4ar,7s,7as)-1-{[(1r,3as,3bs,7r,9ar,9bs,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-4,7-dimethyl-hexahydro-1h-cyclopenta[c]pyran-3-one

C39H64O3 (580.4855193999999)


   

5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl)oxy]oxane-2-carboxylic acid

5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl)oxy]oxane-2-carboxylic acid

C47H76O17 (912.5082246)


   

7-(prop-1-en-2-yl)-6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2,4,7,9,13,15,17-heptaene-1,16-diol

7-(prop-1-en-2-yl)-6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2,4,7,9,13,15,17-heptaene-1,16-diol

C20H16O5 (336.0997686)


   

(2r,3r,4s,5s,6r)-2-{[(2r,3e)-4-[(1s,2s,4r)-2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl]but-3-en-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

(2r,3r,4s,5s,6r)-2-{[(2r,3e)-4-[(1s,2s,4r)-2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl]but-3-en-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C19H32O8 (388.20970719999997)


   

(1r,4e,6s,7r,17s)-4-ethylidene-6,7-dimethyl-3,8-dioxo-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-en-7-yl acetate

(1r,4e,6s,7r,17s)-4-ethylidene-6,7-dimethyl-3,8-dioxo-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-en-7-yl acetate

C20H27NO6 (377.18382820000005)


   

7-{[6-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one

7-{[6-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one

C26H28O14 (564.1478988)


   

(8r,9r,11z,14r,15s,16r)-11-ethylidene-8,15-dihydroxy-8,9-dimethyl-6,13-dioxa-1-azatricyclo[12.2.1.0⁴,¹⁶]heptadec-3-ene-7,12-dione

(8r,9r,11z,14r,15s,16r)-11-ethylidene-8,15-dihydroxy-8,9-dimethyl-6,13-dioxa-1-azatricyclo[12.2.1.0⁴,¹⁶]heptadec-3-ene-7,12-dione

C18H25NO6 (351.168179)


   

2-{16-hydroxy-6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2,4,7,9,13,15,17-heptaen-7-yl}propane-1,2-diol

2-{16-hydroxy-6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2,4,7,9,13,15,17-heptaen-7-yl}propane-1,2-diol

C20H18O6 (354.1103328)


   

1-[(1r,12r)-16-hydroxy-6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2,4,7,9,13,15,17-heptaen-7-yl]ethanone

1-[(1r,12r)-16-hydroxy-6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2,4,7,9,13,15,17-heptaen-7-yl]ethanone

C19H14O5 (322.0841194)


   

(1r,4r,5r,6r,16r)-5,6-dihydroxy-4-isopropyl-5,6-dimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

(1r,4r,5r,6r,16r)-5,6-dihydroxy-4-isopropyl-5,6-dimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

C18H27NO6 (353.1838282)


   

4-ethylidene-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate

4-ethylidene-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate

C21H29NO7 (407.1943924)


   

(1r,4r,5s,6s,16s)-6-ethyl-5,6-dihydroxy-4-isopropyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

(1r,4r,5s,6s,16s)-6-ethyl-5,6-dihydroxy-4-isopropyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

C18H27NO6 (353.1838282)


   

7-(methoxymethyl)-2,3,5,7a-tetrahydro-1h-pyrrolizin-1-ol

7-(methoxymethyl)-2,3,5,7a-tetrahydro-1h-pyrrolizin-1-ol

C9H15NO2 (169.110273)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O11 (448.100557)


   

(2s,5s)-2-amino-5-hydroxyhexanoic acid

(2s,5s)-2-amino-5-hydroxyhexanoic acid

C6H13NO3 (147.0895388)


   

4-(1-chloroethyl)-4,7-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

4-(1-chloroethyl)-4,7-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

C18H26ClNO6 (387.1448566)


   

(1r,4e)-4-ethylidene-7-hydroxy-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

(1r,4e)-4-ethylidene-7-hydroxy-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

C17H23NO5 (321.1576148)


   

7-hydroxy-4,5,6-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

7-hydroxy-4,5,6-trimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

C17H25NO5 (323.173264)


   

5,6-dihydroxy-6-(1-hydroxyethyl)-4-isopropyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

5,6-dihydroxy-6-(1-hydroxyethyl)-4-isopropyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

C18H27NO7 (369.1787432)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3r,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3r,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O11 (448.100557)


   

1-(chloromethyl)-5-methylideneazocane

1-(chloromethyl)-5-methylideneazocane

C9H16ClN (173.0971206)


   

(1s,4s,5r,6r,16s)-5,6-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

(1s,4s,5r,6r,16s)-5,6-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-ene-3,7-dione

C16H23NO6 (325.1525298)


   

(4e)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

(4e)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11-ene-3,8-dione

C18H25NO5 (335.173264)


   

(8r,9r,11e,14r,15s)-11-ethylidene-8,15-dihydroxy-8,9-dimethyl-6,13-dioxa-1-azatricyclo[12.2.1.0⁴,¹⁶]heptadec-3-ene-7,12-dione

(8r,9r,11e,14r,15s)-11-ethylidene-8,15-dihydroxy-8,9-dimethyl-6,13-dioxa-1-azatricyclo[12.2.1.0⁴,¹⁶]heptadec-3-ene-7,12-dione

C18H25NO6 (351.168179)


   

(2s)-2-[(3r,3as,5as,5br,7ar,9r,10s,11ar,11br,13br)-3,9,10-trihydroxy-3a,5a,5b,8,8,11a-hexamethyl-1h,2h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13bh-cyclopenta[a]chrysen-3-yl]propanoic acid

(2s)-2-[(3r,3as,5as,5br,7ar,9r,10s,11ar,11br,13br)-3,9,10-trihydroxy-3a,5a,5b,8,8,11a-hexamethyl-1h,2h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13bh-cyclopenta[a]chrysen-3-yl]propanoic acid

C30H48O5 (488.3501558)


   

(1s,10z)-6-hydroxy-4,5,6,13-tetramethyl-2,8-dioxa-13-azabicyclo[8.5.1]hexadec-10-ene-3,7,16-trione

(1s,10z)-6-hydroxy-4,5,6,13-tetramethyl-2,8-dioxa-13-azabicyclo[8.5.1]hexadec-10-ene-3,7,16-trione

C17H25NO6 (339.168179)


   

1-{16-hydroxy-6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2,4,7,9,13,15,17-heptaen-7-yl}ethanone

1-{16-hydroxy-6,11,19-trioxapentacyclo[10.8.0.0²,¹⁰.0⁵,⁹.0¹³,¹⁸]icosa-2,4,7,9,13,15,17-heptaen-7-yl}ethanone

C19H14O5 (322.0841194)


   

4-ethylidene-7-hydroxy-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11(17)-ene-3,8-dione

4-ethylidene-7-hydroxy-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.0¹⁴,¹⁷]heptadec-11(17)-ene-3,8-dione

C17H23NO5 (321.1576148)


   

3,4,5-trihydroxy-6-{[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy}oxane-2-carboxylic acid

3,4,5-trihydroxy-6-{[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy}oxane-2-carboxylic acid

C21H18O11 (446.0849078)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.105642)


   

6-hydroxy-4,5,6-trimethyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate

6-hydroxy-4,5,6-trimethyl-3,7-dioxo-2,8-dioxa-13-azatricyclo[8.5.1.0¹³,¹⁶]hexadec-10-en-5-yl acetate

C18H25NO7 (367.163094)


   

2-[(3,4-dihydroxyphenyl)methyl]-2-hydroxybutanedioic acid

2-[(3,4-dihydroxyphenyl)methyl]-2-hydroxybutanedioic acid

C11H12O7 (256.05830019999996)