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Thunbergia laurifolia

Thunbergia laurifolia - 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 UUID64404389cd2b1118805754
Scientific name Thunbergia laurifolia
Authority Lindl.
First published in Gard. Chron. 1856: 260 (1856)

Description Top

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Synonyms Top

Scientific name Authority First published in
Thunbergia harrisii Hook.f. Bot. Mag. 83: t. 4998 (1857)
Thunbergia grandiflora var. laurifolia (Lindl.) Benoist Fl. Indo-Chine 4: 618 1935

Common names Top

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Language Common/alternative name
English laurel clockvine
Arabic تونبرغية غارية الأوراق
Malayalam ബ്ലൂ ട്രംപറ്റ് വൈൻ
Malay pokok trumpet
Thai คาย
Thai รางจืด
Thai รางเย็น
Thai ย่ำแย้
Thai ดุเหว่า
Thai ขอบชะนาง, เครือเขาเขียว, ยาเขียว
Thai กำลังช้างเผือก น้ำนอง
Chinese 樟叶邓伯花
Chinese 桂叶老鸦嘴
Chinese 樟葉鄧伯花
Chinese 桂叶牵牛
Chinese 桂叶山牵牛
Chinese 月桂藤

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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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-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Nicobar Nicobar
      • Vietnam
    • Malesia
      • Malaya
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Marianas
    • South-central Pacific
      • Cook Islands
      • Society Islands
    • Southwestern Pacific
      • Fiji
      • Vanuatu
      • Wallis-Futuna Islands
  • Southern America
    • Caribbean
      • Leeward Islands
      • Windward Islands
    • Western South America
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001045078
UNII R046WN33OE
USDA Plants THLA6
Tropicos 102966
INPN 446882
KEW urn:lsid:ipni.org:names:56339-1
The Plant List tro-102966
Open Tree Of Life 299125
NCBI Taxonomy 504053
Nature Serve 2.160423
IPNI 56339-1
iNaturalist 169743
GBIF 5415460
Freebase /m/0fzbh3
EPPO THNLA
EOL 481547
USDA GRIN 36609
Wikipedia Thunbergia_laurifolia

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
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Phenolic Compounds and Antioxidant Capacity Comparison of Wild-Type and Yellow-Leaf gl1 Mutant of Lagerstroemia indica Li S, Yin M, Wang P, Gao L, Lv F, Yang R, Li Y, Wang Q, Li L, Liu Y, Wang S Plants (Basel) 20-Jan-2024
PMCID:PMC10818265
doi:10.3390/plants13020315
PMID:38276772
Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Pharm Biol 22-Dec-2023
PMCID:PMC10763916
doi:10.1080/13880209.2023.2292261
PMID:38131672
Anti-inflammatory activity of verbascoside- and isoverbascoside-rich Lamiales medicinal plants Pongkitwitoon B, Putalun W, Triwitayakorn K, Kitisripanya T, Kanchanapoom T, Boonsnongcheep P Heliyon 13-Dec-2023
PMCID:PMC10770615
doi:10.1016/j.heliyon.2023.e23644
PMID:38187323
Plant Extracts as Skin Care and Therapeutic Agents Michalak M Int J Mol Sci 22-Oct-2023
PMCID:PMC10607442
doi:10.3390/ijms242015444
PMID:37895122
The Optimal Dosage of Fermented Herbal Extract on Growth and Feed Efficiency of Nile Tilapia (Oreochromis niloticus) Fujaya Y, Hidayani AA, Sari DK, Aslamyah S, Rukminasari N, Muthalib A, Cristianto S, Defista E, Fazhan H, Waiho K Trop Life Sci Res 21-Jul-2023
PMCID:PMC10743046
doi:10.21315/tlsr2023.34.2.3
PMID:38144381
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Photoprotection and Antiaging Activity of Extracts from Honeybush (Cyclopia sp.)—In Vitro Wound Healing and Inhibition of the Skin Extracellular Matrix Enzymes: Tyrosinase, Collagenase, Elastase and Hyaluronidase Hering A, Stefanowicz-Hajduk J, Gucwa M, Wielgomas B, Ochocka JR Pharmaceutics 19-May-2023
PMCID:PMC10221029
doi:10.3390/pharmaceutics15051542
PMID:37242784
Metabolomic profile, anti-trypanosomal potential and molecular docking studies of Thunbergia grandifolia El-Nashar HA, Sayed AM, El-Sherief HA, Rateb ME, Akil L, Khadra I, Majrashi TA, Al-Rashood ST, Binjubair FA, El Hassab MA, Eldehna WM, Abdelmohsen UR, Mostafa NM J Enzyme Inhib Med Chem 20-Apr-2023
PMCID:PMC10120545
doi:10.1080/14756366.2023.2199950
PMID:37080775
DNA barcoding in herbal medicine: Retrospective and prospective Chen S, Yin X, Han J, Sun W, Yao H, Song J, Li X J Pharm Anal 05-Apr-2023
PMCID:PMC10257146
doi:10.1016/j.jpha.2023.03.008
PMID:37305789
Plant-Derived Products with Therapeutic Potential against Gastrointestinal Bacteria Qassadi FI, Zhu Z, Monaghan TM Pathogens 15-Feb-2023
PMCID:PMC9967904
doi:10.3390/pathogens12020333
PMID:36839605
Medicinal plants used by rural Thai people to treat non-communicable diseases and related symptoms Nguanchoo V, Balslev H, Sadgrove NJ, Phumthum M Heliyon 04-Jan-2023
PMCID:PMC9850000
doi:10.1016/j.heliyon.2022.e12758
PMID:36685400
Promoting rational herb-drug use through pharmacy-led advice and home visits in NCD patients Ploylearmsang C, Kanjanasilp J, Tadtiyanant J, Sisala P Pharm Pract (Granada) 18-Nov-2022
PMCID:PMC9891797
doi:10.18549/PharmPract.2022.4.2747
PMID:36793912
Acute and sub-chronic toxicity study of Rang Chuet (Thunbergia laurifolia Lindl.) extracts and its antioxidant activities Posridee K, Oonsivilai A, Oonsivilai R Toxicol Rep 09-Nov-2022
PMCID:PMC9743654
doi:10.1016/j.toxrep.2022.11.002
PMID:36518438
Standardized Thunbergia laurifolia Extract Inhibits PM2.5-Induced Oxidative Stress by Regulating p62–KEAP1–NRF2 Signaling Pathway JIRABANJERDSIRI B, SRIRATANASAK N, TOWIWAT P, PRUEKSASIT T, SUKRONG S, CHANVORACHOTE P In Vivo 03-Nov-2022
PMCID:PMC9677787
doi:10.21873/invivo.13009
PMID:36309371

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 / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-Hex-2-enoxy-6-(hydroxymethyl)oxane-3,4,5-triol 78302325 Click to see CCCC=CCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
2-Hexenyl-beta-glucopyranoside 6450053 Click to see CCCC=CCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
2-Hexoxy-6-(hydroxymethyl)oxane-3,4,5-triol 4462283 Click to see CCCCCCOC1C(C(C(C(O1)CO)O)O)O 264.31 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
Hexyl beta-D-glucopyranoside 181215 Click to see CCCCCCOC1C(C(C(C(O1)CO)O)O)O 264.31 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5R,9S,10S,15S)-15-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 139031795 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
Grandifloric acid 433554 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,7R,7aS)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-carboxylic acid 6325299 Click to see C1CC(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
(1S,4aR,7S,7aS)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-carboxylic acid 101202242 Click to see C1CC(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
1-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-carboxylic acid 20979870 Click to see C1CC(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
2-[2-[(5,6-Dihydroxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl)oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 74029716 Click to see C1=COC(C2C1(C(C3C2O3)O)O)OC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O 510.40 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
3'-O-beta-Glucopyranosyl-stilbericoside 6325264 Click to see C1=COC(C2C1(C(C3C2O3)O)O)OC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O 510.40 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
Benzyl b-sophoropyranoside 73157713 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
Benzyl-beta-d-glucopyranoside 13254166 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
Zizybeoside I 11972301 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 4475102 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(02)00139-5
Vicenin-2 3084407 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(02)00139-5

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