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Bauhinia saccocalyx

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 UUID643fdc29d3dc0532897543
Scientific name Bauhinia saccocalyx
Authority Pierre
First published in Fl. Forest. Cochinch.: t. 400B (1899)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Pauletia saccocalyx (Pierre) A.Schmitz Bull. Soc. Roy. Bot. Belgique110: 15 (1977)

Common names Top

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Language Common/alternative name
Thai เสี้ยวเครือ

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000199581
Tropicos 13043248
KEW urn:lsid:ipni.org:names:481650-1
The Plant List ild-46073
Open Tree Of Life 3916325
NCBI Taxonomy 1707764
IPNI 481650-1
iNaturalist 430714
GBIF 2953590
EOL 654890

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
A New Benzo[6,7]oxepino[3,2-b] Pyridine Derivative Induces Apoptosis in Canine Mammary Cancer Cell Lines Jianpraphat N, Supsavhad W, Ngernmeesri P, Siripattarapravat K, Soontararak S, Akrimajirachoote N, Phaochoosak N, Jermnak U Animals (Basel) 25-Jan-2024
PMCID:PMC10854894
doi:10.3390/ani14030386
PMID:38338029
Dibenzo[b,f]oxepine Molecules Used in Biological Systems and Medicine Krawczyk H Int J Mol Sci 27-Jul-2023
PMCID:PMC10418896
doi:10.3390/ijms241512066
PMID:37569442
Gram-Scale Total Synthesis of TAB with Cardioprotective Activity and the Structure-Activity Relationship of Its Analogs Sun Z, Sun Z, Wu D, Yi F, Wu H, Ma G, Xu X Molecules 04-Jul-2023
PMCID:PMC10343337
doi:10.3390/molecules28135197
PMID:37446862
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Monitoring of forage and nutrition before and after reintroduction of banteng (Bos javanicus d’ Alton, 1823) to Salakphra Wildlife Sanctuary, Thailand Chaiyarat R, Sakchan P, Panprayun G, Thongthip N, Nakbun S Sci Rep 07-Jul-2020
PMCID:PMC7341747
doi:10.1038/s41598-020-67942-2
PMID:32636423
Enhancing bio-recovery of bioactive compounds extracted from Citrus medica L. Var. sarcodactylis: optimization performance of integrated of pulsed-ultrasonic/microwave technique Mahdi AA, Rashed MM, Al-Ansi W, Ahmed MI, Obadi M, Jiang Q, Raza H, Wang H 08-Mar-2019
PMCID:PMC7149043
doi:10.1007/s11694-019-00083-x
Anthropogenic effects on a tropical forest according to the distance from human settlements Popradit A, Srisatit T, Kiratiprayoon S, Yoshimura J, Ishida A, Shiyomi M, Murayama T, Chantaranothai P, Outtaranakorn S, Phromma I Sci Rep 05-Oct-2015
PMCID:PMC5155698
doi:10.1038/srep14689
PMID:26434950
New Short Strategy for the Synthesis of the Dibenz[b,f]oxepin Scaffold Moreno DR, Giorgi G, Salas CO, Tapia RA Molecules 29-Nov-2013
PMCID:PMC6270238
doi:10.3390/molecules181214797
PMID:24352054
Bauhinoxepins A and B: New Antimycobacterial Dibenzo[<i>b</i>,<i>f</i>]oxepins from <i>Bauhinia saccocalyx</i> Prasat Kittakoop, Sombat Nopichai, Nuntawan Thongon, Panarat Charoenchai, Yodhathai Thebtaranonth Wiley 04-Feb-2004
doi:10.1002/HLCA.200490006

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 / Benzoxepines / Dibenzoxepines
Bauhinoxepin A 11723631 Click to see CC1=C(C2=C(C=CC3=C(C=CC=C3O2)O)C4=C1OC(C=C4)(C)C)O 322.40 unknown https://doi.org/10.1002/HLCA.200490006
Bauhinoxepin B 3009552 Click to see CC1=C(C=C2C=CC3=C(C=CC(=C3O)CC=C(C)C)OC2=C1OC)O 338.40 unknown https://doi.org/10.1002/HLCA.200490006

Gallery Top

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Collections Top

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