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Phaius mishmensis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fe6c222fb6636637474
Scientific name Phaius mishmensis
Authority Rchb.f.
First published in Bonplandia (Hannover) 5: 43 (1857)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Limatodis mishmensis Lindl. & Paxton Paxton's Fl. Gard. 3: 36 (1852)
Phaius augustinianus Klotzsch Allg. Gartenzeitung 24: 9 (1856)
Phaius crinita (Gagnep.) Seidenf. Bull. Mus. Natl. Hist. Nat., Sér. 3, Bot. 71(5): 141 (1972 publ. 1973)
Phaius cupreus Rchb.f. Bonplandia (Hannover) 3: 226 (1855)
Phaius gracilis Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 322 (1911)
Phaius roseus Rolfe Bull. Misc. Inform. Kew 1893: 6 (1893)
Calanthe crinita Gagnep. Bull. Mus. Natl. Hist. Nat. , sér. 2, 3: 322 (1931)
Calanthe ramosa Gagnep. Bull. Mus. Natl. Hist. Nat. , sér. 2, 22: 626 (1951)
Calanthe mishmensis (Lindl. & Paxton) M.W.Chase, Christenh. & Schuit. Phytotaxa 472: 163 (2020)

Common names Top

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Language Common/alternative name
Chinese 細莖鶴頂蘭
Chinese 紫花鹤顶兰
Chinese 细茎鹤顶兰

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000268062
Tropicos 23507590
KEW urn:lsid:ipni.org:names:650444-1
The Plant List kew-151055
Open Tree Of Life 366348
NCBI Taxonomy 679631
IPNI 650444-1
iNaturalist 542721
GBIF 2836505
EOL 1135609
CMAUP NPO4147

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
Recent advances of tryptanthrin and its derivatives as potential anticancer agents Zhou X RSC Med Chem 04-Jan-2024
PMCID:PMC11042161
doi:10.1039/d3md00698k
PMID:38665827
Identification, Biological Function Profiling and Biosynthesis of Secondary Metabolites in Medicinal Orchids Li K, Wu F, Chen M, Xiao Z, Xu Y, Xu M, Liu J, Xu D Metabolites 07-Jul-2023
PMCID:PMC10385179
doi:10.3390/metabo13070829
PMID:37512536
Dihydroxyquingdainone Induces Apoptosis in Leukaemia and Lymphoma Cells via the Mitochondrial Pathway in a Bcl-2- and Caspase-3-Dependent Manner and Overcomes Resistance to Cytostatic Drugs In Vitro Baas J, Bieringer S, Frias C, Frias J, Soehnchen C, Urmann C, Ritter S, Riepl H, Prokop A Molecules 08-Aug-2022
PMCID:PMC9370279
doi:10.3390/molecules27155038
PMID:35956988
Natural products as a therapy to combat against SARS-CoV-2 virus infection Malviya S, Parihar A, Parihar DS, Khan R Computational Approaches for Novel Therapeutic and Diagnostic Designing to Mitigate SARS-CoV-2 Infection 15-Jul-2022
PMCID:PMC9300459
doi:10.1016/B978-0-323-91172-6.00017-0
The Natural Alkaloid Tryptanthrin Induces Apoptosis-like Death in Leishmania spp. Garcia AR, Silva-Luiz YP, Alviano CS, Alviano DS, Vermelho AB, Rodrigues IA Trop Med Infect Dis 20-Jun-2022
PMCID:PMC9231190
doi:10.3390/tropicalmed7060112
PMID:35736990
Orchidaceae-Derived Anticancer Agents: A Review Śliwiński T, Kowalczyk T, Sitarek P, Kolanowska M Cancers (Basel) 31-Jan-2022
PMCID:PMC8833831
doi:10.3390/cancers14030754
PMID:35159021
Tryptanthrin from microwave-assisted reduction of isatin using solid-state-supported sodium borohydride: DFT calculations, molecular docking and evaluation of its analgesic and anti-inflammatory activity Obafemi CA, Adegbite OB, Fadare OA, Iwalewa EO, Omisore NO, Sanusi K, Yilmaz Y, Ceylan Ü Heliyon 31-Dec-2020
PMCID:PMC7788106
doi:10.1016/j.heliyon.2020.e05756
PMID:33437886
Chemical Constituents of Phaius mishmensis Jao CW, Hung TH, Chang CF, Chuang TH Molecules 23-Nov-2016
PMCID:PMC6272941
doi:10.3390/molecules21111605
PMID:27886100
Three pairs of alkaloid enantiomers from the root of Isatis indigotica Liu Y, Wang X, Chen M, Lin S, Li L, Shi J Acta Pharm Sin B 11-Feb-2016
PMCID:PMC4788710
doi:10.1016/j.apsb.2016.01.003
PMID:27006898
Complete Chloroplast Genome Sequence of an Orchid Model Plant Candidate: Erycina pusilla Apply in Tropical Oncidium Breeding Pan IC, Liao DC, Wu FH, Daniell H, Singh ND, Chang C, Shih MC, Chan MT, Lin CS PLoS One 04-Apr-2012
PMCID:PMC3319614
doi:10.1371/journal.pone.0034738
PMID:22496851
Isolation, structure elucidation, and synthesis of cytotoxic tryptanthrin analogues from Phaius mishmensis. Jao CW, Lin WC, Wu YT, Wu PL J Nat Prod 01-Jul-2008
doi:10.1021/NP800064W
PMID:18507473

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
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
(1R,5S)-3-oxa-12,20-diazapentacyclo[10.8.0.01,5.06,11.014,19]icosa-6,8,10,14,16,18-hexaene-4,13-dione 162029060 Click to see C1C23C(C4=CC=CC=C4N2C(=O)C5=CC=CC=C5N3)C(=O)O1 292.29 unknown https://doi.org/10.1021/NP800064W
3-Oxa-12,20-diazapentacyclo[10.8.0.01,5.06,11.014,19]icosa-6,8,10,14,16,18-hexaene-4,13-dione 24970703 Click to see 292.29 unknown https://doi.org/10.1021/NP800064W
Phaitanthrin D 44561298 Click to see 292.29 unknown https://doi.org/10.1021/NP800064W
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines / Indoloquinazolines
6-(3-Oxoindolin-2-ylidene) indolo(2,1-b)quinazolin-12-one 126674 Click to see 363.40 unknown https://doi.org/10.1021/NP800064W
6-Hydroxy-6-(2-oxocyclopentyl)indolo[2,1-b]-quinazolin-12-one 24970647 Click to see 332.40 unknown via CMAUP database
6-Hydroxy-6-(2-oxodecyl)indolo[2,1-b]quinazolin-12-one 24970646 Click to see 404.50 unknown via CMAUP database
6-Hydroxy-6-(3-oxopentan-2-yl)indolo[2,1-b]quinazolin-12-one 24970701 Click to see CCC(=O)C(C)C1(C2=CC=CC=C2N3C1=NC4=CC=CC=C4C3=O)O 334.40 unknown via CMAUP database
7-Hydroxytryptanthrin 24970644 Click to see C1=CC=C2C(=C1)C(=O)N3C4=C(C(=CC=C4)O)C(=O)C3=N2 264.23 unknown https://doi.org/10.1021/NP800064W
Candidine 5320815 Click to see 363.40 unknown https://doi.org/10.1021/NP800064W
methyl (12R)-12-hydroxy-6-oxoindolo[2,1-b]quinazoline-12-carboxylate 154496999 Click to see 308.29 unknown https://doi.org/10.1021/NP800064W
methyl (12S)-12-hydroxy-6-oxoindolo[2,1-b]quinazoline-12-carboxylate 162851265 Click to see COC(=O)C1(C2=CC=CC=C2N=C3N1C4=CC=CC=C4C3=O)O 308.29 unknown https://doi.org/10.1021/NP800064W
methyl 2-[(6S)-6-hydroxy-12-oxoindolo[2,1-b]quinazolin-6-yl]acetate 132552070 Click to see 322.30 unknown https://doi.org/10.1021/NP800064W
Methylisatoid 384867 Click to see 308.29 unknown https://doi.org/10.1021/NP800064W
Phaitanthrin A 154497199 Click to see 306.30 unknown https://doi.org/10.1021/NP800064W
Phaitanthrin E 24970645 Click to see COC(=O)C1=C2NC3=CC=CC=C3C(=O)N2C4=CC=CC=C41 292.29 unknown https://doi.org/10.1021/NP800064W
Phaitanthrins A 24970702 Click to see 306.30 unknown https://doi.org/10.1021/NP800064W
Phaitanthrins B 24970643 Click to see COC(=O)CC1(C2=CC=CC=C2N3C1=NC4=CC=CC=C4C3=O)O 322.30 unknown https://doi.org/10.1021/NP800064W
Tryptanthrin 73549 Click to see 248.24 unknown https://doi.org/10.1021/NP800064W

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