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Costus spicatus

Costus spicatus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ff48394329081305600
Scientific name Costus spicatus
Authority (Jacq.) Sw.
First published in Prodr. Veg. Ind. Occ. : 11 (1788)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Alpinia spicata Jacq. Enum. syst. pl. 11
Amomum petiolatum Lam. Encycl. 136
Costus cylindricus Jacq. Fragm. Bot. : 54 (1806)
Costus micranthus Gagnep. Bull. Soc. Bot. France 50: 586 (1903)
Costus quartus Roem. & Schult. Syst. Veg., ed. 15 bis 1: 26 (1817)

Common names Top

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Language Common/alternative name
English spiked spiralflag
Arabic قسط شائك
ht kann dlo
Indonesian pacing
Portuguese cana do brejo
Chinese 穗花闭鞘姜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Puerto Rico
      • Windward Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000363620
UNII NU8S11314R
USDA Plants COSP4
Tropicos 34500638
INPN 447791
KEW urn:lsid:ipni.org:names:329964-2
The Plant List kew-234781
Open Tree Of Life 620937
NCBI Taxonomy 328782
IPNI 329964-2
iNaturalist 276567
GBIF 2756925
Freebase /m/0g57v_s
EPPO CQTSP
EOL 1122452
USDA GRIN 426906
Wikipedia Costus_spicatus

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Desmodium styracifolium: Botanical and ethnopharmacological insights, phytochemical investigations, and prospects in pharmacology and pharmacotherapy Opryshko V, Prokhach A, Akimov O, Riabushko M, Kostenko H, Kostenko V, Mishchenko A, Solovyova N, Kostenko V Heliyon 20-Jan-2024
PMCID:PMC10838797
doi:10.1016/j.heliyon.2024.e25058
PMID:38317880
Use of medicinal plants during COVID-19 pandemic in Brazil da Silva AM, Horsth AL, Timóteo ÉD, Faria RJ, Bazoni PS, Meira EF, dos Santos JB, da Silva MR Sci Rep 02-Oct-2023
PMCID:PMC10545667
doi:10.1038/s41598-023-43673-y
PMID:37783716
Urinary Tract Infections Caused by Uropathogenic Escherichia coli: Mechanisms of Infection and Treatment Options Zhou Y, Zhou Z, Zheng L, Gong Z, Li Y, Jin Y, Huang Y, Chi M Int J Mol Sci 23-Jun-2023
PMCID:PMC10341809
doi:10.3390/ijms241310537
PMID:37445714
Advances in Research on the Regulation of Floral Development by CYC-like Genes Chai Y, Liu H, Chen W, Guo C, Chen H, Cheng X, Chen D, Luo C, Zhou X, Huang C Curr Issues Mol Biol 02-Mar-2023
PMCID:PMC10047570
doi:10.3390/cimb45030131
PMID:36975501
In vitro effects of European and Latin-American medicinal plants in CYP3A4 gene expression, glutathione levels, and P-glycoprotein activity Mazzari AL, Lacerda MG, Milton FA, Mulin Montechiari Machado JA, Sinoti SB, Toullec AS, Rodrigues PM, Neves FD, Simeoni LA, Silveira D, Prieto JM Front Pharmacol 05-Oct-2022
PMCID:PMC9579425
doi:10.3389/fphar.2022.826395
PMID:36278236
Correlation between Inflorescence Architecture and Floral Asymmetry—Evidence from Aberrant Flowers in Canna L. (Cannaceae) Yu Q, Zhao T, Zhao H, Specht CD, Tian X, Liao J Plants (Basel) 26-Sep-2022
PMCID:PMC9571657
doi:10.3390/plants11192512
PMID:36235378
The genetic mechanisms underlying the convergent evolution of pollination syndromes in the Neotropical radiation of Costus L. Valderrama E, Landis JB, Skinner D, Maas PJ, Maas-van de Kramer H, André T, Grunder N, Sass C, Pinilla-Vargas M, Guan CJ, Phillips HR, de Almeida AM, Specht CD Front Plant Sci 08-Sep-2022
PMCID:PMC9493542
doi:10.3389/fpls.2022.874322
PMID:36161003
Pest categorisation of Pulvinaria psidii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Maiorano A, Papachristos D, MacLeod A EFSA J 12-Aug-2022
PMCID:PMC9372818
doi:10.2903/j.efsa.2022.7526
PMID:35978619
Nephroprotective effect of polyphenol-rich extract of Costus spicatus in cisplatin-induced nephrotoxicity in Wistar albino rats Ali A, Ali A, Ahmad W, Amir M, Ashraf K, Wahab S, Alam P, Abutahir, Ahamad A 3 Biotech 25-Jul-2022
PMCID:PMC9314513
doi:10.1007/s13205-022-03233-z
PMID:35903285
Local Knowledge and Use of Medicinal Plants in a Rural Community in the Agreste of Paraíba, Northeast Brazil da Costa Ferreira E, Anselmo MD, Guerra NM, Marques de Lucena C, Felix CD, Bussmann RW, Paniagua-Zambrana NY, Paiva de Lucena RF Evid Based Complement Alternat Med 29-Dec-2021
PMCID:PMC8731275
doi:10.1155/2021/9944357
PMID:35003314
Temporal assessment of the medicinal plants trade in public markets of the state of Paraíba, northeastern Brazil da Costa Ferreira E, de Lucena RF, Bussmann RW, Paniagua-Zambrana NY, da Cruz DD J Ethnobiol Ethnomed 19-Dec-2021
PMCID:PMC8684639
doi:10.1186/s13002-021-00496-3
PMID:34924006
Evaluation of the inhibitory potentials of selected compounds from Costus spicatus (Jacq.) rhizome towards enzymes associated with insulin resistance in polycystic ovarian syndrome: an in silico study Femi-Olabisi FJ, Ishola AA, Faokunla O, Agboola AO, Babalola BA J Genet Eng Biotechnol 23-Nov-2021
PMCID:PMC8611123
doi:10.1186/s43141-021-00276-2
PMID:34812979
How does urbanization affect perceptions and traditional knowledge of medicinal plants? Arjona-García C, Blancas J, Beltrán-Rodríguez L, López Binnqüist C, Colín Bahena H, Moreno-Calles AI, Sierra-Huelsz JA, López-Medellín X J Ethnobiol Ethnomed 03-Aug-2021
PMCID:PMC8330055
doi:10.1186/s13002-021-00473-w
PMID:34344391
Atheroprotective Properties of Costus spicatus (Jacq.) Sw. in Female Rats Lorençone BR, Guarnier LP, Palozi RA, Romão PV, Marques AA, Klider LM, Souza RI, dos Santos AC, Tirloni CA, Cassemiro NS, Silva DB, Manfron Budel J, Gasparotto Junior A Life (Basel) 08-Mar-2021
PMCID:PMC8001518
doi:10.3390/life11030212
PMID:33800454
What’s in a name? Revisiting medicinal and religious plants at an Amazonian market Geertsma IP, Françozo M, van Andel T, Rodríguez MA J Ethnobiol Ethnomed 05-Feb-2021
PMCID:PMC7866673
doi:10.1186/s13002-021-00433-4
PMID:33546714

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162861427 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(CO8)(CO)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1049.20 unknown https://doi.org/10.1016/S0031-9422(99)00077-1
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 100936159 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(CO7)(CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1049.20 unknown https://doi.org/10.1055/S-2006-960782
2-[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-2-(hydroxymethyl)-6-[[6-methoxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 85246810 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(CO8)(CO)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1049.20 unknown https://doi.org/10.1016/S0031-9422(99)00077-1
2-[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-[[6-methoxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163090793 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(CO7)(CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1049.20 unknown https://doi.org/10.1055/S-2006-960782
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,3',5,7-Tetrahydroxyflavone 9860659 Click to see C1=CC(=CC(=C1)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
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/S0031-9422(99)00441-0
Tamarixetin 5281699 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3-Hydroxy-4-methoxyphenyl)-3-(beta-D-glucopyranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one 12443209 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
3-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 162927287 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)OC)O)CO)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one 162969805 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)OC)CO)O)O)O)O)O 608.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
3-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 162927286 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)OC)O)CO)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 101022693 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)OC)O)CO)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3-hydroxyphenyl)chromen-4-one 162905485 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=CC=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one 101022694 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)OC)CO)O)O)O)O)O 608.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 139031045 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
3-[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)chromen-4-one 162895015 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)OC)CO)O)O)O)O)O 622.60 unknown https://doi.org/10.1016/S0367-326X(00)00161-1
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3-hydroxyphenyl)chromen-4-one 162905484 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=CC=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one 74977600 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)OC)CO)O)O)O)O)O 608.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
4-methoxy-kaempferol-3-O-hexoside 74978140 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
5,7-dihydroxy-2-(3-hydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162936981 Click to see C1=CC(=CC(=C1)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
5,7-Dihydroxy-2-(3-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162936980 Click to see C1=CC(=CC(=C1)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
Isorhamnetin-3-O-neohesperidoside 24204448 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)OC)O)CO)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
kaempferide 3-O-glucoside 90659152 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
Kaempferide 3-O-neohesperidoside 44257994 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)OC)CO)O)O)O)O)O 608.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
Quercetin 3-alloside 12304327 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
Quercetin 3-O-alpha-rhamnopyranosyl-(1-2)-beta-galactopyranoside 5748416 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(99)00441-0
Tamarixin 12443210 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(99)00441-0

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