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Tinospora baenzigeri

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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 UUID643ffecb8df5a687666023
Scientific name Tinospora baenzigeri
Authority Forman
First published in Kew Bull. 36: 399 (1981)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Thai ชิงช้าชาลี

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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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
    • Indo-China
      • Thailand
      • Vietnam
    • Malesia
      • Christmas Island
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000456716
KEW urn:lsid:ipni.org:names:898933-1
The Plant List kew-2517142
Open Tree Of Life 6130210
NCBI Taxonomy 1960964
IPNI 898933-1
GBIF 3830870
Elurikkus 420613

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
DNA barcoding: an efficient technology to authenticate plant species of traditional Chinese medicine and recent advances Zhu S, Liu Q, Qiu S, Dai J, Gao X Chin Med 28-Sep-2022
PMCID:PMC9514984
doi:10.1186/s13020-022-00655-y
PMID:36171596
Natural Bioactive Cinnamoyltyramine Alkylamides and Co-Metabolites Evidente A, Masi M Biomolecules 25-Nov-2021
PMCID:PMC8698393
doi:10.3390/biom11121765
PMID:34944409
Antimalarial Activity of Tinospora baenzigeri against Plasmodium berghei-Infected Mice Ounjaijean S, Kotepui M, Somsak V J Trop Med 05-Sep-2019
PMCID:PMC6748209
doi:10.1155/2019/5464519
PMID:31582992
Species identification approach for both raw materials and end products of herbal supplements from Tinospora species Osathanunkul M, Osathanunkul R, Madesis P BMC Complement Altern Med 27-Mar-2018
PMCID:PMC5870811
doi:10.1186/s12906-018-2174-0
PMID:29587839
Clerodane diterpenes: sources, structures, and biological activities Li R, Morris-Natschke SL, Lee KH Nat Prod Rep 18-Jul-2016
PMCID:PMC5154363
doi:10.1039/c5np00137d
PMID:27433555
Rearranged clerodane diterpenes from Tinospora baenzigeri Pittaya Tuntiwachwuttikul, Nicha Boonrasri, John B. Bremner, Walter C. Taylor Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00376-3
New rearranged clerodane diterpenes from Tinospora baenzigeri. Tuntiwachwuttikul P, Taylor WC Chem Pharm Bull (Tokyo) 01-Jul-2001
doi:10.1248/CPB.49.854
PMID:11456091

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
(1S,2S,4S,10R,11R,15S)-4-(furan-2-yl)-2,10-dimethyl-11-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,13-dioxatetracyclo[8.6.0.02,7.011,15]hexadec-7-ene-6,12-dione 162939844 Click to see CC12CC=C3C(=O)OC(CC3(C1CC4C2(C(=O)OC4)OC5C(C(C(C(O5)CO)O)O)O)C)C6=CC=CO6 520.50 unknown https://doi.org/10.1016/S0031-9422(99)00376-3
4-(Furan-2-yl)-2,10-dimethyl-11-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,13-dioxatetracyclo[8.6.0.02,7.011,15]hexadec-7-ene-6,12-dione 162939843 Click to see CC12CC=C3C(=O)OC(CC3(C1CC4C2(C(=O)OC4)OC5C(C(C(C(O5)CO)O)O)O)C)C6=CC=CO6 520.50 unknown https://doi.org/10.1016/S0031-9422(99)00376-3
4-(Furan-3-yl)-2,10-dimethyl-11-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,13-dioxatetracyclo[8.6.0.02,7.011,15]hexadec-7-ene-6,12-dione 162989573 Click to see CC12CC=C3C(=O)OC(CC3(C1CC4C2(C(=O)OC4)OC5C(C(C(C(O5)CO)O)O)O)C)C6=COC=C6 520.50 unknown https://doi.org/10.1016/S0031-9422(99)00376-3
Baenzigeroside A 101009665 Click to see CC12CC=C3C(=O)OC(CC3(C1CC4C2(C(=O)OC4)OC5C(C(C(C(O5)CO)O)O)O)C)C6=COC=C6 520.50 unknown https://doi.org/10.1248/CPB.49.854
https://doi.org/10.1016/S0031-9422(99)00376-3
methyl (1R,2S,5S,7S,8S,9S,10S)-5-(furan-3-yl)-7,9-dimethyl-3-oxo-8-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-4,11-dioxatricyclo[7.2.1.02,7]dodecane-10-carboxylate 101105821 Click to see CC12CC(OC(=O)C1C3CC(C2CCCOC4C(C(C(C(O4)CO)O)O)O)(C(O3)C(=O)OC)C)C5=COC=C5 554.60 unknown https://doi.org/10.1248/CPB.49.854
methyl (1S,2S,5S,7S,8S,9R,10S)-5-(furan-3-yl)-7,9-dimethyl-3-oxo-8-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-4,11-dioxatricyclo[7.2.1.02,7]dodecane-10-carboxylate 10053384 Click to see CC12CC(OC(=O)C1C3CC(C2CCCOC4C(C(C(C(O4)CO)O)O)O)(C(O3)C(=O)OC)C)C5=COC=C5 554.60 unknown https://doi.org/10.1248/CPB.49.854
Methyl 5-(furan-3-yl)-7,9-dimethyl-3-oxo-8-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl]-4,11-dioxatricyclo[7.2.1.02,7]dodecane-10-carboxylate 85104671 Click to see CC12CC(OC(=O)C1C3CC(C2CCCOC4C(C(C(C(O4)CO)O)O)O)(C(O3)C(=O)OC)C)C5=COC=C5 554.60 unknown https://doi.org/10.1248/CPB.49.854
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(1S,2S,4S,10R,11R,15S)-4-(furan-2-yl)-11-hydroxy-2,10-dimethyl-5,13-dioxatetracyclo[8.6.0.02,7.011,15]hexadec-7-ene-6,12-dione 163021520 Click to see CC12CC=C3C(=O)OC(CC3(C1CC4C2(C(=O)OC4)O)C)C5=CC=CO5 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00376-3
(1S,2S,4S,10R,11R,15S)-4-(furan-3-yl)-11-hydroxy-2,10-dimethyl-5,13-dioxatetracyclo[8.6.0.02,7.011,15]hexadec-7-ene-6,12-dione 15489041 Click to see CC12CC=C3C(=O)OC(CC3(C1CC4C2(C(=O)OC4)O)C)C5=COC=C5 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00376-3
4-(Furan-2-yl)-11-hydroxy-2,10-dimethyl-5,13-dioxatetracyclo[8.6.0.02,7.011,15]hexadec-7-ene-6,12-dione 163021519 Click to see CC12CC=C3C(=O)OC(CC3(C1CC4C2(C(=O)OC4)O)C)C5=CC=CO5 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00376-3
4-(Furan-3-yl)-11-hydroxy-2,10-dimethyl-5,13-dioxatetracyclo[8.6.0.02,7.011,15]hexadec-7-ene-6,12-dione 162862431 Click to see CC12CC=C3C(=O)OC(CC3(C1CC4C2(C(=O)OC4)O)C)C5=COC=C5 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00376-3
> Organoheterocyclic compounds / Oxepanes
methyl (1R,2S,5S,7S,8S,9S,10S)-5-(furan-3-yl)-8-(3-hydroxypropyl)-7,9-dimethyl-3-oxo-4,11-dioxatricyclo[7.2.1.02,7]dodecane-10-carboxylate 101105820 Click to see CC12CC(OC(=O)C1C3CC(C2CCCO)(C(O3)C(=O)OC)C)C4=COC=C4 392.40 unknown https://doi.org/10.1248/CPB.49.854
methyl (1S,2S,5S,7S,8S,9R,10S)-5-(furan-3-yl)-8-(3-hydroxypropyl)-7,9-dimethyl-3-oxo-4,11-dioxatricyclo[7.2.1.02,7]dodecane-10-carboxylate 11090466 Click to see CC12CC(OC(=O)C1C3CC(C2CCCO)(C(O3)C(=O)OC)C)C4=COC=C4 392.40 unknown https://doi.org/10.1248/CPB.49.854
Methyl 5-(furan-3-yl)-8-(3-hydroxypropyl)-7,9-dimethyl-3-oxo-4,11-dioxatricyclo[7.2.1.02,7]dodecane-10-carboxylate 85395169 Click to see CC12CC(OC(=O)C1C3CC(C2CCCO)(C(O3)C(=O)OC)C)C4=COC=C4 392.40 unknown https://doi.org/10.1248/CPB.49.854

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