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Veratrum maackii

Veratrum maackii - 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
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Details Top

Internal ID UUID64402419891b4530113762
Scientific name Veratrum maackii
Authority Regel
First published in Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 4(4): 154 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Veratrum maackii f. atropurpureum (Honda) T.Shimizu New Alp. Fl. Japan in Color 2: 358 (1983):.
Veratrum oblongum var. macranthum O.Loes. Repert. Spec. Nov. Regni Veg. 24: 68. 1927
Veratrum maackii var. macranthum (O.Loes.) Nakai Rep. Inst. Sci. Res. Manchoukou 1: 339 1937
Veratrum maackii f. macranthum (O.Loes.) T.Shimizu Acta Phytotax. Geobot. 18: 167 1960
Veratrum maackii subsp. maackioides (O.Loes.) Zimm. Lloydia 24: 10. 1961 (1961)
Veratrum nigrum subsp. maackii (Regel) Kitam. Acta Phytotax. Geobot. 22: 71. 1966 (1966)
Veratrum longibracteatum var. atropurpureum Honda Bot. Mag. (Tokyo) 49: 700 1935
Veratrum versicolor f. brunneum Nakai Rep. Inst. Sci. Res. Manchoukuo 1: 341 1937
Veratrum nigrum var. maackii (Regel) Maxim.

Common names Top

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Language Common/alternative name
Russian Чемерица Маака
Chinese 藜芦
Chinese 毛穗藜芦

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Veratrum maackii var. japonicum (Baker) T.Shimizu Acta Phytotax. Geobot. 18: 167 1960
Veratrum maackii var. maackii Unknown
Veratrum maackii var. parviflorum (Maxim. ex Miq.) H.Hara Sci. Res. Ozegahara Moor : 476 (1954)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000751700
Tropicos 18404330
KEW urn:lsid:ipni.org:names:543507-1
The Plant List kew-291226
Open Tree Of Life 112384
Observations.org 132820
NCBI Taxonomy 82471
IPNI 543507-1
iNaturalist 508496
GBIF 2742059
EPPO VEAMC
EOL 1083439
Elurikkus 294226
USDA GRIN 423585

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
Comparative transcriptome analysis of Veratrum maackii and Veratrum nigrum reveals multiple candidate genes involved in steroidal alkaloid biosynthesis Wang D, Yu Z, Guan M, Cai Q, Wei J, Ma P, Xue Z, Ma R, Oksman-Caldentey KM, Rischer H Sci Rep 21-May-2023
PMCID:PMC10200796
doi:10.1038/s41598-023-35429-5
PMID:37211560
Detection of Highly Poisonous Nerium oleander Using Quantitative Real-Time PCR with Specific Primers Bai X, Wang G, Ren Y, Han J Toxins (Basel) 10-Nov-2022
PMCID:PMC9696062
doi:10.3390/toxins14110776
PMID:36356026
Development of real-time PCR based molecular markers for two medicinal herb Artemisia species A. capillaris and A. iwayomogi Kim YD, Uh YR, Jang CS Food Sci Biotechnol 21-Sep-2022
PMCID:PMC9807703
doi:10.1007/s10068-022-01166-0
PMID:36606092
Chemistry and bioactivities of natural steroidal alkaloids Xiang ML, Hu BY, Qi ZH, Wang XN, Xie TZ, Wang ZJ, Ma DY, Zeng Q, Luo XD Nat Prod Bioprospect 15-Jun-2022
PMCID:PMC9198197
doi:10.1007/s13659-022-00345-0
PMID:35701630
Development and application of DNA markers to detect adulteration with Scopolia japonica in the medicinal herb Atractylodes lancea Oh SH, Kim YD, Jang CS Food Sci Biotechnol 26-Nov-2021
PMCID:PMC8733082
doi:10.1007/s10068-021-01008-5
PMID:35059233
Oxyresveratrol: Sources, Productions, Biological Activities, Pharmacokinetics, and Delivery Systems Likhitwitayawuid K Molecules 11-Jul-2021
PMCID:PMC8307110
doi:10.3390/molecules26144212
PMID:34299485
Development and characterization of microsatellite markers for Veratrum maackii (Melanthiaceae) Li Y, Iijima S, Maki M Appl Plant Sci 05-Jun-2015
PMCID:PMC4467762
doi:10.3732/apps.1500030
PMID:26082881
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Chen S, Kim DK, Chase MW, Kim JH PLoS One 18-Mar-2013
PMCID:PMC3605904
doi:10.1371/journal.pone.0059472
PMID:23544071
Studies on the constituents of Veratrum plants. I. Constituents of Veratrum maackii Reg.; isolation and structure determination of a new alkaloid, maackinine. Weijie ZAHO, Yasuhiro TEZUKA, Tohru KIKUCHI, Jun CHEN, Yongtian GUO Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.37.2920
Veramadines A and B, New Steroidal Alkaloids from Veratrum maackii var. japonicum. Tanaka N, Suto S, Kobayashi J Chem Pharm Bull (Tokyo) 01-Jan-2011
doi:10.1248/CPB.59.909
PMID:21720048
Steroidal alkaloids from Veratrum dahuricum Jian Tang, Hui-Liang Li, Yun-Heng Shen, Run-hui Liu, Xi-ke Xu, Wei-Dong Zhang Springer Science and Business Media LLC 01-Oct-2008
doi:10.1007/S10600-008-9082-3
Epimeric (20R,20S)-Verazine Isolated from Veratrum maackii: Two-Dimensional NMR Studies and Total Assignment of 1H- and 13C-Resonances. Han X, Rüegger H Planta Med 01-Oct-1992
doi:10.1055/S-2006-961511
PMID:17226501

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / 22,26-epiminocholestanes
(20S,25S)-22,26-iminocholesta-5,22(N)-dien-3beta-ol 70699389 Click to see CC1CCC(=NC1)C(C)C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C 397.60 unknown https://doi.org/10.1007/S10600-008-9082-3
https://doi.org/10.1248/CPB.37.2920
(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(1R)-1-[(3S)-3-methyl-2,3,4,5-tetrahydropyridin-6-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163075037 Click to see CC1CCC(=NC1)C(C)C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C 397.60 unknown https://doi.org/10.1055/S-2006-961511
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(10,12,13,14,23-Pentahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl) 2-methylbut-2-enoate 78410119 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C 575.70 unknown https://doi.org/10.1248/CPB.59.909
(1R,2S,6S,9S,10S,11R,12S,14S,15S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-17-ene-10,12,20-triol 162945498 Click to see CC1CCC2C(C3C(CC4C5CC=C6CC(CCC6(C5CC4C3CN2C1)C)O)O)(C)O 429.60 unknown https://doi.org/10.1248/CPB.59.909
(1S,2S,6S,9S,10S,11R,12S,13S,14S,15S,18S,19S,22S,23S,25R)-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosane-10,12,13,14,22,23-hexol 162881092 Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC7C5(CCC(C7(O6)O)O)C)(C)O 493.60 unknown https://doi.org/10.1248/CPB.37.2920
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S,25R)-16-acetyloxy-10,12,14,23-tetrahydroxy-6,10,19-trimethyl-13-[(Z)-2-methylbut-2-enoyl]oxy-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (Z)-2-methylbut-2-enoate 101835363 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4C(C3)OC(=O)C)O)OC(=O)C(=CC)C)O)(C)O)C)O)C 715.90 unknown https://doi.org/10.1248/CPB.37.2920
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S,25R)-16-acetyloxy-10,12,14,23-tetrahydroxy-6,10,19-trimethyl-22-[(Z)-2-methylbut-2-enoyl]oxy-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-13-yl] (2R)-2-methylbutanoate 101306698 Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(=CC)C)O)C)OC(=O)C)O)O 717.90 unknown https://doi.org/10.1248/CPB.37.2920
[16-Acetyloxy-10,12,14,23-tetrahydroxy-6,10,19-trimethyl-13-(2-methylbut-2-enoyloxy)-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] 2-methylbut-2-enoate 162884732 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4C(C3)OC(=O)C)O)OC(=O)C(=CC)C)O)(C)O)C)O)C 715.90 unknown https://doi.org/10.1248/CPB.37.2920
[16-Acetyloxy-10,12,14,23-tetrahydroxy-6,10,19-trimethyl-22-(2-methylbut-2-enoyloxy)-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-13-yl] 2-methylbutanoate 75094328 Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(=CC)C)O)C)OC(=O)C)O)O 717.90 unknown https://doi.org/10.1248/CPB.37.2920
6,10,19-Trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosane-10,12,13,14,22,23-hexol 4486612 Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC7C5(CCC(C7(O6)O)O)C)(C)O 493.60 unknown https://doi.org/10.1248/CPB.37.2920
7,11,19-Trimethyl-26-oxa-13-azaheptacyclo[21.2.1.02,18.03,16.06,15.08,13.019,24]hexacosane-3,5,7,22-tetrol 162848947 Click to see CC1CCC2C(C3C(CC4(C(C3CN2C1)CC5C4C6CC7C5(CCC(C7O6)O)C)O)O)(C)O 461.60 unknown https://doi.org/10.1248/CPB.59.909
Angeloylzygadenine 6441115 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C 575.70 unknown https://doi.org/10.1248/CPB.37.2920
Cevane-3,4,14,15,16,20-hexol, 4,9-epoxy-, 3-(3,4-dimethoxybenzoate), (3beta,4alpha,15alpha,16beta)- 162954883 Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC7C5(CCC(C7(O6)O)OC(=O)C8=CC(=C(C=C8)OC)OC)C)(C)O 657.80 unknown https://doi.org/10.1248/CPB.59.909
Zygadenine 442987 Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC7C5(CCC(C7(O6)O)O)C)(C)O 493.60 unknown https://doi.org/10.1248/CPB.37.2920
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13S,14S,17R)-10,13-dimethyl-17-[(1S)-1-[(3S)-3-methyl-2,3,4,5-tetrahydropyridin-6-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101835364 Click to see CC1CCC(=NC1)C(C)C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C)C 559.80 unknown https://doi.org/10.1248/CPB.37.2920
2-[[10,13-dimethyl-17-[1-(3-methyl-2,3,4,5-tetrahydropyridin-6-yl)ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14488686 Click to see CC1CCC(=NC1)C(C)C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C)C 559.80 unknown https://doi.org/10.1248/CPB.37.2920

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