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Isatis costata

Isatis costata - 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 UUID644021f2e77fe817106190
Scientific name Isatis costata
Authority C.A.Mey.
First published in Fl. Altaic. 3: 204 (1831)

Description Top

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Synonyms Top

Scientific name Authority First published in
Isatis costata var. costata C.A.Mey.
Isatis costata var. lasiocarpa (Ledeb.) N.Busch
Isatis costata f. lasiocarpa (Ledeb.) N.Busch Fol. Sibir. et Orient. Extr. 1: 161 1913
Isatis costata var. leiocarpa Ledeb.

Common names Top

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Language Common/alternative name
Chinese 三肋菘蓝
Chinese 肋果菘蓝

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

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
  • Asia-temperate
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Buryatiya
      • Krasnoyarsk
      • Tuva
      • West Siberia
  • Europe
    • Eastern Europe
      • Central European Russia
      • East European Russia
      • Krym
      • South European Russia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000732377
Tropicos 4102168
KEW urn:lsid:ipni.org:names:285765-1
The Plant List kew-2866927
Open Tree Of Life 3932101
Observations.org 118973
NCBI Taxonomy 1439905
IPNI 285765-1
GBIF 5374266
EOL 2886641
Elurikkus 529979
USDA GRIN 20457
CMAUP NPO21106

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
2-Oxindole and related heterocycles: synthetic methodologies for their natural products and related derivatives Sharma S, Monga Y, Gupta A, Singh S RSC Adv 11-May-2023
PMCID:PMC10173257
doi:10.1039/d3ra02217j
PMID:37179999
Urease and α-Chymotrypsin Inhibitory Activities and Molecular Docking Studies of Alkaloids Isolated from Medicinal Plant Isatis minima Bunge Fozia F, Ahmad I, Haq ZU, Wadood A, Khan HU, Ahmed M, Jamila N, Ullah R, Alotaibi A, Sultan MA Evid Based Complement Alternat Med 15-Jun-2022
PMCID:PMC9217576
doi:10.1155/2022/1904874
PMID:35754682
Computational Workflow to Study the Diversity of Secondary Metabolites in Fourteen Different Isatis Species Huang D, Zhang C, Chen J, Xiao Y, Li M, Sun L, Qiu S, Chen W Cells 06-Mar-2022
PMCID:PMC8909408
doi:10.3390/cells11050907
PMID:35269530
Chemistry of trisindolines: natural occurrence, synthesis and bioactivity Wati FA, Santoso M, Moussa Z, Fatmawati S, Fadlan A, Judeh ZM RSC Adv 21-Jul-2021
PMCID:PMC9037102
doi:10.1039/d1ra03091d
PMID:35478918
Folk nomenclature of plants in Cistanche deserticola-associated community in South Gobi, Mongolia Mandakh U, Battseren M, Ganbat D, Ayanga T, Adiya Z, Borjigidai A, Long C Plant Divers 06-Oct-2020
PMCID:PMC7936101
doi:10.1016/j.pld.2020.09.008
PMID:33733011
Enzyme Inhibition Studies of Oxindole Alkaloids from Isatis costata Abdul Malik, Itrat Fatima, Ijaz Ahmad, Sarfraz A. Nawaz, Nighat Afza, Ghosia Luttfullah, M. Iqbal Choudhary The Japan Institute of Heterocyclic Chemistry 17-Feb-2009
doi:10.3987/COM-06-10747
Isatinones A and B, new antifungal oxindole alkaloids from Isatis costata. Fatima I, Ahmad I, Anis I, Malik A, Afza N Molecules 06-Feb-2007
PMCID:PMC6149419
doi:10.3390/12020155
PMID:17846565
Isatinones A and B, New Antifungal Oxindole Alkaloids from Isatis costata Fatima I, Ahmad I, Anis I, Malik A, Afza N Molecules 06-Feb-2007
PMCID:PMC6149419
doi:10.3390/12020155
PMID:17846565

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
methyl 4-hydroxy-3-[(3E)-3-(methoxymethylidene)-2-oxoindol-1-yl]benzoate 11845224 Click to see COC=C1C2=CC=CC=C2N(C1=O)C3=C(C=CC(=C3)C(=O)OC)O 325.30 unknown https://doi.org/10.3987/COM-06-10747
Methyl 4-hydroxy-3-[3-(methoxymethylidene)-2-oxoindol-1-yl]benzoate 73123909 Click to see COC=C1C2=CC=CC=C2N(C1=O)C3=C(C=CC(=C3)C(=O)OC)O 325.30 unknown https://doi.org/10.3987/COM-06-10747
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16-diol 46865976 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
Chlorogenin 12303065 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1 432.60 unknown via CMAUP database
Gitogenin 441887 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown via CMAUP database
Hecogenin 91453 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown via CMAUP database
Manogenin 10253011 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 446.60 unknown via CMAUP database
Rockogenin 167555 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CCC6C5(CCC(C6)O)C)O)C)C)OC1 432.60 unknown via CMAUP database
Sarsasapogenin 92095 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Smilagenin 91439 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Tigogenin 99516 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown via CMAUP database
Yuccagenin 3083608 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CC(C(C6)O)O)C)C)C)OC1 430.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Camassioside 101620741 Click to see CC(C)CC(=O)CC(C)C1C(CC2C1(CCC3C2C(C=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)O)C)OC6C(C(C(C(O6)CO)O)O)O 756.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25R)-3beta-[4-O-[2-O-(3-O-beta-D-Xylopyranosyl-beta-D-glucopyranosyl)-3-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl]-beta-D-galactopyranosyloxy]-5alpha-spirostane 21625854 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(CO2)O)O)O)O)O)O)C)C)C)OC1 1167.30 unknown via CMAUP database
(25R)-3beta-[4-O-[2-O-beta-D-Glucopyranosyl-3-O-(4-O-alpha-L-rhamnopyranosyl-beta-D-xylopyranosyl)-beta-D-glucopyranosyl]-beta-D-galactopyranosyloxy]-5alpha-spirostan-2alpha-ol 71716476 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)OC2C(C(C(C(O2)C)O)O)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)C)C)OC1 1197.30 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-3-hydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21603422 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1 903.10 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15S,16R,18R)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10605143 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C)OC1 756.90 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21603426 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 unknown via CMAUP database
[(25R)-12-Oxo-5beta-spirostane-3beta-yl]2-O-beta-D-glucopyranosyl-beta-D-galactopyranoside 101243911 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 754.90 unknown via CMAUP database
[(25R)-12beta-Hydroxy-5beta-spirostane-3beta-yl]2-O-(beta-D-glucopyranosyl)-beta-D-glucopyranoside 101784690 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)O)C)C)OC1 756.90 unknown via CMAUP database
[(25R)-26-(beta-D-Glucopyranosyloxy)-5beta-furosta-20(22)-ene-3beta-yl]2-O-(beta-D-glucopyranosyl)-beta-D-glucopyranoside 101784691 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)CCC(C)COC8C(C(C(C(O8)CO)O)O)O 903.10 unknown via CMAUP database
12-Oxo-5beta-spirosta-25(27)-ene-3beta-yl 2-O,3-O-bis(beta-D-glucopyranosyl)-beta-D-glucopyranoside 101784689 Click to see CC1C2C(CC3C2(C(=O)CC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC19CCC(=C)CO9 915.00 unknown via CMAUP database
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->3)]-beta-D-galactopyranoside 21603424 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1 903.10 unknown via CMAUP database
Smilagenin 3-O-beta-D-glucopyranosyl-(1->2)-beta-D-galactopyranoside 10628815 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 unknown via CMAUP database
Timosaponin A-III 15953793 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives
[(2S)-2-ethylhexyl] 2-[4-[(E)-(2-oxo-1H-indol-3-ylidene)-phenylmethoxy]phenyl]acetate 163194886 Click to see CCCCC(CC)COC(=O)CC1=CC=C(C=C1)OC(=C2C3=CC=CC=C3NC2=O)C4=CC=CC=C4 483.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149419/
2-ethylhexyl 2-[4-[(2-oxo-1H-indol-3-ylidene)-phenylmethoxy]phenyl]acetate 75252059 Click to see CCCCC(CC)COC(=O)CC1=CC=C(C=C1)OC(=C2C3=CC=CC=C3NC2=O)C4=CC=CC=C4 483.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149419/
3-[methoxy(phenyl)methylidene]-1H-indol-2-one 67005459 Click to see COC(=C1C2=CC=CC=C2NC1=O)C3=CC=CC=C3 251.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149419/
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
3,3-Bis(1H-indole-3-yl)-2-indolinone 2883607 Click to see C1=CC=C2C(=C1)C(=CN2)C3(C4=CC=CC=C4NC3=O)C5=CNC6=CC=CC=C65 363.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149419/
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
isatinone A 46913217 Click to see COC(=C1C2=CC=CC=C2NC1=O)C3=CC=CC=C3 251.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149419/
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2'R,3R)-4-[2-[(2'R,3R)-2'-(4-Hydroxyphenyl)-4',6,6'-trihydroxy-2-oxo-7-methoxyspiro[benzofuran-3(2H),3'(2'H)-benzofuran]-4-yl]ethenyl]-2'-(4-hydroxyphenyl)-4',6,6'-trihydroxy-2-oxospiro[benzofuran-3(2H),3'(2'H)-benzofuran] 17757603 Click to see COC1=C(C=C(C2=C1OC(=O)C23C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)C=CC6=C7C(=CC(=C6)O)OC(=O)C78C(OC9=CC(=CC(=C89)O)O)C1=CC=C(C=C1)O)O 810.70 unknown via CMAUP database
(2'R,3S)-4-[2-[(2'R,3S)-2'-(4-Hydroxyphenyl)-4',6,6'-trihydroxy-2-oxo-7-methoxyspiro[benzofuran-3(2H),3'(2'H)-benzofuran]-4-yl]ethenyl]-2'-(4-hydroxyphenyl)-4',6,6'-trihydroxy-2-oxospiro[benzofuran-3(2H),3'(2'H)-benzofuran] 17755939 Click to see COC1=C(C=C(C2=C1OC(=O)C23C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)C=CC6=C7C(=CC(=C6)O)OC(=O)C78C(OC9=CC(=CC(=C89)O)O)C1=CC=C(C=C1)O)O 810.70 unknown via CMAUP database
Gloriosaol D 102380006 Click to see COC1=C(C=C(C2=C1OC(=O)C23C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)C=CC6=C7C(=CC(=C6)O)OC(=O)C78C(OC9=CC(=CC(=C89)O)O)C1=CC=C(C=C1)O)O 810.70 unknown via CMAUP database

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