Fagopyrum acutatum - Unknown
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Internal ID UUID64401c11a19f1475262653
Scientific name Fagopyrum acutatum
Authority Mansf. ex K.Hammer
First published in Verz. Landwirtsch. Gärtn. Kulturpfl. , ed. 2, 1: 121 (1986)

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Synonyms Top

Scientific name Authority First published in
Polygonum acutatum Lehm. Nov. Stirp. Pug. 1: 28 (1828)
Polygonum tristachyum Baker J. Bot. 20: 244 (1882)
Polygonum volubile Gilib. Exerc. Phyt. 2: 435. 1792
Polygonum dibotrys D.Don Prodr. Fl. Nepal. : 73 (1825)
Polygonum cymosum Trevir. Index Seminum (WROCL, Wratislaviensi) 1823: 2 (1824)
Polygonum labordei H.Lév. & Vaniot Bull. Acad. Int. Géogr. Bot. 11: 344 (1902)
Coccoloba cymosa Lour. Fl. Cochinch. : 240 (1790)
Fagopyrum chinense Raf. Fl. Tellur. 3: 10 (1837)
Fagopyrum dibotrys (D.Don) Hara Fl. E. Himal. : 69 (1966)
Fagopyrum megaspartanium Q.F.Chen Bot. J. Linn. Soc. 130: 62 (1999)
Fagopyrum pilus Q.F.Chen Bot. J. Linn. Soc. 130: 62 (1999)
Fagopyrum triangulare Meisn. ex Wall. Pl. Asiat. Rar. 3: 63 (1832)
Fagopyrum tristachyum Gross Bull. Acad. Int. Géogr. Bot. 23: 26 (1913)
Oxygonum tristachyum (Baker) H.Perrier Biogéogr. Madag. : 59 (1936)
Polygonum tristachyum H.Lév. Repert. Spec. Nov. Regni Veg. 11: 297 (1912)
Polygonum volubile Turcz. Bull. Soc. Imp. Naturalistes Moscou 14: 77 (1840)

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000685440
Tropicos 50254025
KEW urn:lsid:ipni.org:names:943686-1
The Plant List kew-2807293
Open Tree Of Life 7049752
NCBI Taxonomy 2291126
IPNI 943686-1
GBIF 4036422
EPPO FAGCY
USDA GRIN 463663
CMAUP NPO26242

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India Ralte L, Sailo H, Singh YT J Ethnobiol Ethnomed 03-Jan-2024
PMCID:PMC10765666
doi:10.1186/s13002-023-00642-z
PMID:38172927
Towards a better understanding of Fagopyrum dibotrys: a systematic review Zhang LL, He Y, Sheng F, Hu YF, Song Y, Li W, Chen J, Zhang J, Zou L Chin Med 16-Sep-2021
PMCID:PMC8447528
doi:10.1186/s13020-021-00498-z
PMID:34530893
Monpa, memory, and change: an ethnobotanical study of plant use in Mêdog County, South-east Tibet, China Li S, Zhang Y, Guo Y, Yang L, Wang Y J Ethnobiol Ethnomed 30-Jan-2020
PMCID:PMC6993401
doi:10.1186/s13002-020-0355-7
PMID:32000826
An ethnobotanical study of medicinal plants used to treat skin diseases in northern Pakistan Malik K, Ahmad M, Zafar M, Ullah R, Mahmood HM, Parveen B, Rashid N, Sultana S, Shah SN, Lubna BMC Complement Altern Med 13-Aug-2019
PMCID:PMC6693210
doi:10.1186/s12906-019-2605-6
PMID:31409400
Traditionally used wild edible plants of district Udhampur, J&K, India Bhatia H, Sharma YP, Manhas RK, Kumar K J Ethnobiol Ethnomed 29-Nov-2018
PMCID:PMC6263044
doi:10.1186/s13002-018-0272-1
PMID:30486847
Yao herbal medicinal market during the Dragon Boat Festival in Jianghua County, China Luo B, Liu Y, Liu B, Liu S, Zhang B, Zhang L, Lin C, Liu Y, Kennelly EJ, Guo Z, Long C J Ethnobiol Ethnomed 17-Oct-2018
PMCID:PMC6192344
doi:10.1186/s13002-018-0260-5
PMID:30333030
A new flavonol derivative from Fagopyrum dibotrys Jian Zhang, Zhi-Qi Yin, Peng Cao, You-Bin Li, Jin-Ao Duan Springer Science and Business Media LLC 03-Feb-2009
doi:10.1007/S10600-009-9197-1
Antioxidant phenolic constituents from Fagopyrum dibotrys. Wang KJ, Zhang YJ, Yang CR J Ethnopharmacol 03-Jun-2005
doi:10.1016/J.JEP.2005.02.029
PMID:15894136
Inhibition of tumor growth in vitro by the extract of fagopyrum cymosum (fago-c). Chan PK Life Sci 07-Mar-2003
doi:10.1016/S0024-3205(03)00013-4
PMID:12586222

Phytochemical Profile Top

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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/J.JEP.2005.02.029
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/J.JEP.2005.02.029
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1aR)-1,4abeta,5abeta,6,7,8,8abeta,8b-Octahydro-7,7,8balpha-trimethyl-2beta-methoxycyclopropa[4,5]indeno[5,6-c]furan-5(4H)-one 102074593 Click to see CC1(CC2C(C1)C3(CC34C(C2=O)COC4OC)C)C 264.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
4,4,6a,6b,8a,11,11,14a-octamethyl-2,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1H-picen-3-one 5249513 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(=O)C5(C)C)C)C)C 424.70 unknown https://doi.org/10.1007/S10600-009-9197-1
Glutinone 10071029 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(=O)C5(C)C)C)C)C 424.70 unknown https://doi.org/10.1007/S10600-009-9197-1
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol 5320711 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/J.JEP.2005.02.029
Endotelon 130556 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B4 147299 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin C1 169853 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/J.JEP.2005.02.029
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin 182232 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.JEP.2005.02.029
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1016/J.JEP.2005.02.029
(+)-Catechin gallate 5276454 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
Epicatechin-3-gallate 65056 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S10600-009-9197-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/S0024-3205(03)00013-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-009-9197-1
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-009-9197-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 5480901 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1007/S10600-009-9197-1
Linarin 5317025 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1007/S10600-009-9197-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Caryatin 5489501 Click to see COC1=CC(=CC2=C1C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
3,8-Dihydroxy-10-methoxyisochromeno[4,3-b]chromen-7(5h)-one 139030718 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC(=C4)O)O 312.27 unknown https://doi.org/10.1007/S10600-009-9197-1

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