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Paratinospora sagittata

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 UUID68f90c9e9b6de117118746
Scientific name Paratinospora sagittata
Authority (Oliv.) Wei Wang
First published in Molec. Phylogen. Evol. 109: 18 (2016)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Limacia sagittata Oliv. Hooker's Icon. Pl. 18: t. 1749 (1888)
Tinospora szechuanensis S.Y.Hu J. Arnold Arbor. 35: 196 (1954)
Tinospora sagittata var. leucocarpa Y.Wan ex C.Z.Gao Guihaia 10: 178 (1990)
Tinospora yunnanensis S.Y.Hu J. Arnold Arbor. 35: 197 (1954)
Tinospora craveniana S.Y.Hu J. Arnold Arbor. 35: 194 (1954)
Tinospora imbricata S.Y.Hu J. Arnold Arbor. 35: 195 (1954)
Tinospora capillipes Gagnep. Bull. Soc. Bot. France 55: 44 (1908)
Tinospora intermedia S.Y.Hu J. Arnold Arbor. 35: 196 (1954)
Tinospora sagittata (Oliv.) Gagnep. Bull. Soc. Bot. France 55: 45 (1908)
Tinospora sagittata var. yunnanensis (S.Y.Hu) H.S.Lo Fl. Yunnanica 3: 232 (1983)
Tinospora sagittata var. craveniana (S.Y.Hu) H.S.Lo Icon. Cormophyt. Sin. , Suppl. 1: 490 (1982)

Common names Top

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Language Common/alternative name
English tinospora sagittata yunnanensis
Chinese 峨眉青牛胆
Chinese 大叶藤
Chinese 青牛胆
Chinese 地苦胆
Chinese 金果榄
Chinese 青牛胆（金果榄）
Chinese 云南青牛胆
Chinese 山慈姑

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
Tropicos 50053810
KEW urn:lsid:ipni.org:names:77097819-1
The Plant List kew-2897642
IPNI 77097819-1
GBIF 3830333
Tropicos 50053808
KEW urn:lsid:ipni.org:names:581637-1
The Plant List kew-2516864
NCBI Taxonomy 648882
IPNI 581637-1
GBIF 7268746
EOL 5518182
USDA GRIN 431131
Tropicos 50053811
KEW urn:lsid:ipni.org:names:951911-1
The Plant List kew-2516883
IPNI 951911-1
GBIF 3830311
CMAUP NPO10008
Open Tree Of Life 899457
World Flora Online wfo-1000036334

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_035771175.1 ASM3577117v1 Chromosome Huazhong Agricultural University 2024-01-24 31 1.21 Gb

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Recent Applications of Protoberberines as Privileged Starting Materials for the Development of Novel Broad-Spectrum Antiviral Agents: A Concise Review (2017–2023) Valipour M, Zakeri Khatir Z, Abdollahi E, Ayati A ACS Pharmacol Transl Sci 28-Dec-2023
PMCID:PMC10789142
doi:10.1021/acsptsci.3c00292
PMID:38230282
Clerodane Furanoditerpenoids from Tinospora bakis (A.Rich.) Miers (Menispermaceae) Kabbashi AS, Sattar MA, Aamer M, Siddiqui NN, Kamran M, Fayaz A, Jahan H, Khan FA, Wang Y Molecules 26-Dec-2023
PMCID:PMC10780120
doi:10.3390/molecules29010154
PMID:38202737
Recent advances towards natural plants as potential inhibitors of SARS-Cov-2 targets He Z, Yuan J, Zhang Y, Li R, Mo M, Wang Y, Ti H Pharm Biol 22-Aug-2023
PMCID:PMC10446791
doi:10.1080/13880209.2023.2241518
PMID:37605622
Anti-Inflammatory and Cytotoxic Activities of Clerodane-Type Diterpenes Martínez-Casares RM, Hernández-Vázquez L, Mandujano A, Sánchez-Pérez L, Pérez-Gutiérrez S, Pérez-Ramos J Molecules 13-Jun-2023
PMCID:PMC10303976
doi:10.3390/molecules28124744
PMID:37375299
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Jatrorrhizine Suppresses Murine-Norovirus-Triggered N-GSDMD-Dependent Pyroptosis in RAW264.7 Macrophages Fu M, Chen N, Zhou Y, Chen S, Xu W, Gong S, Geng L Vaccines (Basel) 12-Jan-2023
PMCID:PMC9866343
doi:10.3390/vaccines11010164
PMID:36680009
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Palmatine Attenuates Metastatic Lung Colonization of Triple Negative Breast Cancer Cells Ativui S, Danquah CA, Ossei PP, Ofori M Front Pharmacol 13-Apr-2022
PMCID:PMC9043321
doi:10.3389/fphar.2022.853230
PMID:35496301
Jatrorrhizine: A Review of Sources, Pharmacology, Pharmacokinetics and Toxicity Zhong F, Chen Y, Chen J, Liao H, Li Y, Ma Y Front Pharmacol 13-Jan-2022
PMCID:PMC8793695
doi:10.3389/fphar.2021.783127
PMID:35095493
Approaches to Decrease Hyperglycemia by Targeting Impaired Hepatic Glucose Homeostasis Using Medicinal Plants Mata-Torres G, Andrade-Cetto A, Espinoza-Hernández F Front Pharmacol 23-Dec-2021
PMCID:PMC8733686
doi:10.3389/fphar.2021.809994
PMID:35002743
The Analgesic Properties of Corydalis yanhusuo Alhassen L, Dabbous T, Ha A, Dang LH, Civelli O Molecules 10-Dec-2021
PMCID:PMC8704877
doi:10.3390/molecules26247498
PMID:34946576
Herbal plants traded at the Kaili medicinal market, Guizhou, China Liu S, Zhang B, Zhou J, Lei Q, Fang Q, Kennelly EJ, Long C J Ethnobiol Ethnomed 29-Nov-2021
PMCID:PMC8628420
doi:10.1186/s13002-021-00495-4
PMID:34844607
Study of Nutraceuticals and Phytochemicals for the Management of Alzheimer's Disease: A Review Ahmad SS, Khalid M, Kamal MA, Younis K Curr Neuropharmacol 15-Nov-2021
PMCID:PMC9185787
doi:10.2174/1570159X19666210215122333
PMID:33588732
Therapeutic Potential of Neoechinulins and Their Derivatives: An Overview of the Molecular Mechanisms Behind Pharmacological Activities Sharifi-Rad J, Bahukhandi A, Dhyani P, Sati P, Capanoglu E, Docea AO, Al-Harrasi A, Dey A, Calina D Front Nutr 16-Jul-2021
PMCID:PMC8322439
doi:10.3389/fnut.2021.664197
PMID:34336908

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
> Alkaloids and derivatives / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1002/RCM.2593
https://doi.org/10.1055/S-2007-969629
(6As)-11-hydroxy-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolinium 161487 Click to see 356.40 unknown https://doi.org/10.1055/S-2007-969629
5-Hydroxy-4,15,16-trimethoxy-10,10-dimethyl-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2(7),3,5,13(17),14-hexaen-10-ium 5315336 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC)C 356.40 unknown https://doi.org/10.1002/RCM.2593
Laurifoline 12305611 Click to see 342.40 unknown via CMAUP database
Laurifoline 37834 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC)C 342.40 unknown https://doi.org/10.1002/RCM.2593
Menisperine 30358 Click to see 356.40 unknown https://doi.org/10.1002/RCM.2593
https://doi.org/10.1055/S-2007-969629
Xanthoplanine 14262868 Click to see 356.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
2-hydroxy-9,10-dimethoxy-6,7-dihydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-3-one 101404949 Click to see 324.30 unknown via CMAUP database
2,3,10-trimethoxy-6,7-dihydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-9-one 101280139 Click to see 338.40 unknown via CMAUP database
Columbamine 72310 Click to see 338.40 unknown https://doi.org/10.1055/S-2007-969629
https://doi.org/10.1002/RCM.2593
Dehydrocorydalmine 3083983 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC(=C(C4=C3)OC)O)OC 338.40 unknown https://doi.org/10.1002/RCM.2593
Dehydrodiscretamine 102316663 Click to see COC1=CC2=C3C=C4C=CC(=C(C4=C[NH+]3CCC2=CC1=O)OC)O 324.30 unknown via CMAUP database
Jatrorrhizine 72323 Click to see 338.40 unknown via CMAUP database
Palmatine 19009 Click to see 352.40 unknown https://doi.org/10.1055/S-2007-969629
Palmatrubine 10547385 Click to see 373.80 unknown via CMAUP database
Stepharanine 10358881 Click to see 324.30 unknown https://doi.org/10.1002/RCM.2593
https://doi.org/10.1055/S-2007-969629
> Alkaloids and derivatives / Yohimbine alkaloids
methyl (1S,3R,4R,4aS,5aS,6R,10aR)-3-hydroxy-1-methyl-2'-oxospiro[1,3,4,4a,5,5a,7,8,10,10a-decahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate 162997621 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(94)00686-N
https://doi.org/10.1055/S-2006-960188
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(1R,2S,3S,5S,8R,11R,12R)-5-(furan-3-yl)-3,11-dimethyl-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione 13858079 Click to see 520.50 unknown https://doi.org/10.1002/HLCA.200890105
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
Palmatoside C 184514 Click to see 520.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
https://doi.org/10.1002/HLCA.200890105
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
[(6R,17R)-13-benzyl-6-hydroxy-4,17-dimethyl-5-oxo-15-prop-1-en-2-yl-12,14,18-trioxapentacyclo[11.4.1.01,10.02,6.011,15]octadeca-3,8-dien-8-yl]methyl 2-(4-hydroxyphenyl)acetate 9916705 Click to see 598.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2S)-2beta-(3-Furyl)-1,4,4aalpha,5,6,6a,9,10,10aalpha,10b-decahydro-6aalpha,10bbeta-dimethyl-4-oxo-9alpha-[(beta-D-glucopyranosyl)oxy]-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester 85446211 Click to see 536.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
https://doi.org/10.1002/HLCA.200890105
methyl (2S,4aS,6aR,9S,10aS,10bS)-2-(furan-3-yl)-6a,10b-dimethyl-4-oxo-9-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 163050733 Click to see CC12CCC3C(=O)OC(CC3(C1CC(C=C2C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C)C5=COC=C5 536.60 unknown https://doi.org/10.1002/HLCA.200890105
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
Tinophylloloside 15694364 Click to see 536.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
CID 12004581 12004581 Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown via CMAUP database
Geniposide 107848 Click to see 388.40 unknown via CMAUP database
methyl (1S,4aS,7aR)-7-(hydroxymethyl)-1-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 51066531 Click to see 388.40 unknown via CMAUP database
methyl (1S,4aS,7aS)-7-(hydroxymethyl)-1-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 78358483 Click to see 388.40 unknown via CMAUP database
Methyl (1S)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 16760120 Click to see 388.40 unknown via CMAUP database
Methyl 7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 3515873 Click to see 388.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see 480.60 unknown via CMAUP database
2beta,3beta,5beta,14,20,22R,25-Heptahydroxycholest-7-en-6-one 441833 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-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 52940117 Click to see 576.80 unknown via CMAUP database
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
cyclo[OLeu-Pro-Phe-N(Me)Val-N(Me)Val-bAla] 73355775 Click to see CC(C)CC1C(=O)N2CCCC2C(=O)NC(C(=O)N(C(C(=O)N(C(C(=O)NCCC(=O)O1)C(C)C)C)C(C)C)C)CC3=CC=CC=C3 655.80 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(-)-Reticuline 440586 Click to see 329.40 unknown via CMAUP database
1-((3-Hydroxy-4-methoxyphenyl)methyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-7-ol 10233 Click to see 329.40 unknown via CMAUP database
Reticuline 439653 Click to see 329.40 unknown via CMAUP database
Tembetarine 167718 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC)C 344.40 unknown https://doi.org/10.1002/RCM.2593
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
10-Hydroxy-2,9-dimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 102316664 Click to see 323.30 unknown https://doi.org/10.1055/S-2007-969629
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see 337.40 unknown https://doi.org/10.1055/S-2007-969629
https://doi.org/10.1002/RCM.2593
> Organoheterocyclic compounds / Naphthopyrans
(1R,2S,3S,5S,8R,10S,11S,12R)-5-(furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione 162961160 Click to see CC12CC(OC(=O)C1CC(C3(C2C4C=CC3(C(=O)O4)O)C)O)C5=COC=C5 374.40 unknown https://doi.org/10.1002/HLCA.200890105
(1S,2R,3R,5R,8R,11S,12S)-5-(furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione 46173925 Click to see 358.40 unknown via CMAUP database
(2S,4AR,6aR,7R,10R,10aS,10bS)-2-(furan-3-yl)-7-hydroxy-6a,10b-dimethyl-4a,5,6,6a,7,10,10a,10b-octahydro-1H-10,7-(epoxymethano)benzo[f]isochromene-4,12(2H)-dione 442015 Click to see CC12CCC3C(=O)OC(CC3(C1C4C=CC2(C(=O)O4)O)C)C5=COC=C5 358.40 unknown https://doi.org/10.1002/RCM.2593
https://doi.org/10.1055/S-2006-960188
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
https://doi.org/10.1002/HLCA.200890105
(3R,5R,8S,11S,12S)-5-(furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione 10406089 Click to see CC12CCC3C(=O)OC(CC3(C1C4C=CC2(C(=O)O4)O)C)C5=COC=C5 358.40 unknown via CMAUP database
5-(Furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione 73813159 Click to see CC12CC(OC(=O)C1CC(C3(C2C4C=CC3(C(=O)O4)O)C)O)C5=COC=C5 374.40 unknown https://doi.org/10.1002/HLCA.200890105
5-(Furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadeca-8,15-diene-7,13-dione 56678199 Click to see CC12CC=C3C(=O)OC(CC3(C1C4C=CC2(C(=O)O4)O)C)C5=COC=C5 356.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
Columbin 188289 Click to see 358.40 unknown via CMAUP database
Fibleucin 44589004 Click to see 356.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
Isocolumbin 12303799 Click to see 358.40 unknown https://doi.org/10.1002/HLCA.200890105
Npc37409 226036 Click to see 358.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
https://doi.org/10.1002/HLCA.200890105
Palmarin 442068 Click to see 374.40 unknown via CMAUP database
SureCN2153783 18502774 Click to see 358.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(2S,4aR,6aR,10aS,10bS)-2-(furan-3-yl)-8-hydroxy-6a,10b-dimethyl-2,4a,5,6,10,10a-hexahydro-1H-benzo[f]isochromene-4,7-dione 163186519 Click to see CC12CCC3C(=O)OC(CC3(C1CC=C(C2=O)O)C)C4=COC=C4 330.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
2-(furan-3-yl)-8-hydroxy-6a,10b-dimethyl-2,4a,5,6,10,10a-hexahydro-1H-benzo[f]isochromene-4,7-dione 163025700 Click to see CC12CCC3C(=O)OC(CC3(C1CC=C(C2=O)O)C)C4=COC=C4 330.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259588/
> Organoheterocyclic compounds / Oxepanes
Udlwcnhpuounnv-zpumpekvsa- 21673189 Click to see CC(=C)C#CC12C(O1)C3C4(CC(C(O3)(C)C)OC(=O)C)C(C2=O)O4 332.30 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
methyl (1S,2S,5R,6R,7R,8S)-6-[(E)-2-(furan-3-yl)ethenyl]-1-hydroxy-2,6-dimethyl-10-oxo-9-oxatricyclo[6.2.2.02,7]dodec-11-ene-5-carboxylate 163189929 Click to see 372.40 unknown https://doi.org/10.1002/HLCA.200890105
methyl (1S,2S,5S,6R,7R,8S)-6-[(E)-2-(furan-3-yl)ethenyl]-1-hydroxy-2,6-dimethyl-10-oxo-9-oxatricyclo[6.2.2.02,7]dodec-11-ene-5-carboxylate 163195527 Click to see 372.40 unknown https://doi.org/10.1002/HLCA.200890105
Methyl 6-[2-(furan-3-yl)ethenyl]-1-hydroxy-2,6-dimethyl-10-oxo-9-oxatricyclo[6.2.2.02,7]dodec-11-ene-5-carboxylate 162893017 Click to see 372.40 unknown https://doi.org/10.1002/HLCA.200890105

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