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Juniperus excelsa

Juniperus excelsa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Juniperus excelsa - 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 UUID643ff38cc9101119976650
Scientific name Juniperus excelsa
Authority M.Bieb.
First published in Tabl. Prov. Mer Casp. : 120 (1798)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Juniperus stricta hort. ex Gordon Pinetum , ed. 2: 144 (1875)
Juniperus venusta hort. ex Gordon Pinetum , ed. 2: 144 (1875)
Juniperus sabina Gueldenst. Reis. Russland 1: 98 (1787)
Juniperus religiosa hort. ex Endl. Syn. Conif. : 26 (1847)
Juniperus lycia Pall. Fl. Ross. 2: 14 (1815)
Juniperus perkinsii hort. ex Gordon Pinetum , ed. 2: 144 (1875)
Juniperus olivieri Carrière Traité Gén. Conif. : 57 (1855)
Juniperus lasdeliana Laws. ex Gordon Pinetum : 105 (1858)
Juniperus isophyllos K.Koch Linnaea 22: 304 (1849)
Juniperus aegaea Griseb. Veg. Erde : 378, 572 (1871)
Sabina religiosa Antoine Cupress.-Gatt. : 47 (1857)
Sabina isophyllos Antoine Cupress.-Gatt. : 48 (1857)
Sabina olivieri Antoine Cupress.-Gatt. : 70 (1857)
Sabina excelsa Antoine Cupress.-Gatt. : 45 (1857)
Juniperus sabina var. taurica Pall. Fl. Ross. 2: 15. 1789
Juniperus sabina var. excelsa (M.Bieb.) Georgi Beschr. Russ. Reich. 3(5): 1358. 1800
Juniperus foetida var. excelsa (M.Bieb.) Spach Ann. Sci. Nat., Bot. , sér. 2, 16: 297 (1841)
Juniperus taurica (Pall.) Lipsky Trav. Exped. Colon. Russe 2, Bot. 6: 185. 1912 (1912)
Juniperus excelsa var. depressa O.Schwarz Repert. Spec. Nov. Regni Veg. 36: 66. 1934
Juniperus excelsa var. pendula (Mulk.) Imkhan. Bot. Zhurn. (Moscow & Leningrad) 75: 407 (1990)
Juniperus excelsa var. stricta R.Sm. Pl. Fir Tribe 19 1874
Juniperus excelsa f. stricta (R.Sm.) Rehder Bibl. Cult. Trees 60 1949
Juniperus sabinnna var. excelsa (M.Bieb.) Georgi Beschr. Russ. Reich. 3(5): 1358 1800

Common names Top

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Language Common/alternative name
English grecian juniper
English greek juniper
English crimean juniper
Arabic عرعر المرتفعات
Arabic اللَّزَّاب
Arabic عرعر متعالي
Azerbaijani hündür ardıc
azb هۆندور آردیج
Bulgarian дървовидна хвойна
German griechischer wacholder
Persian جونیپروس اکسلا
French genévrier grec
Hebrew ערער רם
Hebrew ערער ברושי
Croatian foja divlja
Icelandic grikkjaeinir
Japanese ギリシャビャクシン
Macedonian дива фоја
Norwegian Bokmål gresk einer
Polish jałowiec grecki
Punjab یونانی صنوبر
Russian Можжевельник высокий
Serbo-Croatian divlja foja
Turkish boylu ardıç
Ukrainian Ялівець високий
Uzbek baland archa
Chinese 洒银柏
Chinese 希腊圆柏
Chinese 希臘圓柏

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

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
World Flora Online wfo-0000355502
Canadensys 28046
USDA Plants JUEX2
Tropicos 9400731
INPN 717283
KEW urn:lsid:ipni.org:names:60461568-2
The Plant List kew-2332546
PFAF Juniperus excelsa
PaleoBotany 37854
Open Tree Of Life 283344
Observations.org 124784
NCBI Taxonomy 758917
IUCN Red List 42232
IPNI 262215-1
iNaturalist 135920
GBIF 2684626
Freebase /m/07kqqn
EPPO IUPEX
EOL 1061672
Elurikkus 281792
USDA GRIN 20833
Wikipedia Juniperus_excelsa

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
Linking ecosystems to public health based on combination of social and ecological systems Khosravi Mashizi A, Sharafatmandrad M Sci Rep 30-Apr-2024
PMCID:PMC11061295
doi:10.1038/s41598-024-60814-z
PMID:38689004
The Potential Role of Phytochemicals of Juniperus procera in the Treatment of Ovarian Cancer and the Inhibition of Human Topoisomerase II Alpha Activity Al-Zahrani AA Bioinform Biol Insights 25-Apr-2024
PMCID:PMC11047251
doi:10.1177/11779322241248904
PMID:38681095
The influence of climate change on the future distribution of two Thymus species in Iran: MaxEnt model-based prediction Hosseini N, Ghorbanpour M, Mostafavi H BMC Plant Biol 11-Apr-2024
PMCID:PMC11007882
doi:10.1186/s12870-024-04965-1
PMID:38605338
Cross-cultural ethnobotany of the Baltis and Shinas in the Kharmang district, Trans-Himalaya India-Pakistan border Hussain B, Abbas Z, Alam J, Harun N, Khan SM, Ahmad Z, Han H, Yoo S, Raposo A Heliyon 27-Mar-2024
PMCID:PMC10998220
doi:10.1016/j.heliyon.2024.e28613
PMID:38586350
Comparing the efficacy of fluconazole and cryotherapy Versus cryotherapy alone on treating cutaneous leishmaniasis: a triple-blind randomized clinical trial Parhizkar AR, Sharafi M, Mansuri S, Hadibarhaghtalab M, Afrashteh S, Fatemian H, Chijan MR BMC Infect Dis 20-Mar-2024
PMCID:PMC10953173
doi:10.1186/s12879-024-09211-5
PMID:38509490
The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O Stud Mycol 22-Feb-2024
PMCID:PMC11003443
doi:10.3114/sim.2024.107.03
PMID:38600960
Chemical profile of Juniperus excelsa M. Bieb. essential oil within and between populations and its weed seed suppression effect Semerdjieva I, Zheljazkov VD, Dincheva I, Radoukova T, Astatkie T, Maneva V, Atanasova D, Fidan H, Stankov S, Stoyanova A PLoS One 08-Feb-2024
PMCID:PMC10852245
doi:10.1371/journal.pone.0294126
PMID:38330006
Recent Advances in the Development of Antibiotics-Coated Gold Nanoparticles to Combat Antimicrobial Resistance Sarma PP, Rai A, Baruah PK Antibiotics (Basel) 26-Jan-2024
PMCID:PMC10886052
doi:10.3390/antibiotics13020124
PMID:38391510
The Wild Carrot (Daucus carota): A Phytochemical and Pharmacological Review Ismail J, Shebaby WN, Daher J, Boulos JC, Taleb R, Daher CF, Mroueh M Plants (Basel) 27-Dec-2023
PMCID:PMC10781147
doi:10.3390/plants13010093
PMID:38202401
An update about beneficial effects of medicinal plants in aquaculture: A review Dadras F, Velisek J, Zuskova E Vet Med (Praha) 26-Dec-2023
PMCID:PMC10828785
doi:10.17221/96/2023-VETMED
PMID:38303995
Vegetation–environment interactions: plant species distribution and community assembly in mixed coniferous forests of Northwestern Himalayas Rahman IU, Hart RE, Afzal A, Iqbal Z, Bussmann RW, Ijaz F, Khan MA, Ali H, Rahman SU, Hashem A, Abd-Allah EF, Sher A, Calixto ES Sci Rep 11-Oct-2023
PMCID:PMC10567734
doi:10.1038/s41598-023-42272-1
PMID:37821469
Biosynthesis Strategy of Gold Nanoparticles and Biofabrication of a Novel Amoxicillin Gold Nanodrug to Overcome the Resistance of Multidrug-Resistant Bacterial Pathogens MRSA and E. coli Halawani EM, Alzahrani SS, Gad El-Rab SM Biomimetics (Basel) 25-Sep-2023
PMCID:PMC10603918
doi:10.3390/biomimetics8060452
PMID:37887583
Volatiles of All Native Juniperus Species Growing in Greece—Antimicrobial Properties Fotiadou E, Panou E, Graikou K, Sakellarakis FN, Chinou I Foods 20-Sep-2023
PMCID:PMC10530231
doi:10.3390/foods12183506
PMID:37761215
Mediterranean Plants as Potential Source of Biopesticides: An Overview of Current Research and Future Trends Fragkouli R, Antonopoulou M, Asimakis E, Spyrou A, Kosma C, Zotos A, Tsiamis G, Patakas A, Triantafyllidis V Metabolites 22-Aug-2023
PMCID:PMC10535963
doi:10.3390/metabo13090967
PMID:37755247
Somatic Embryogenesis in Conifers: One Clade to Rule Them All? Fraga HP, Moraes PE, Vieira LD, Guerra MP Plants (Basel) 14-Jul-2023
PMCID:PMC10385530
doi:10.3390/plants12142648
PMID:37514262

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1021/NP50050A053
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4aR,5S,8aR)-2-acetyloxy-1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 100966458 Click to see CC(=O)OC1CCC2(C(C1(C)C(=O)O)CCC(=C)C2CCC(=C)C=C)C 360.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
(1R,2R,4aR,5S,8aS)-2-acetyloxy-1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 162972364 Click to see CC(=O)OC1CCC2(C(C1(C)C(=O)O)CCC(=C)C2CCC(=C)C=C)C 360.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
(1R,2R,8aS)-1-[(3R)-3-hydroxy-3-methylpent-4-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 73114 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
(1R,4aR,5R,8aS)-1,4a-dimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 51668725 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
(1S,4aR,4bR,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carbaldehyde 101630384 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O 286.50 unknown https://doi.org/10.1016/0031-9422(92)83631-8
(1S,4aR,4bR,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 6973653 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0031-9422(92)83631-8
(1S,4aR,5S,8aS)-1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 162907162 Click to see CC12CCCC(C1CCC(=C)C2CCC(=C)C=C)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
(2S,4aS,10aS)-2,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,9,10,10a-tetrahydro-2H-phenanthren-4-one 21632848 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(C(=O)CC(C3(C)C)O)C)O 316.40 unknown https://doi.org/10.1016/0031-9422(92)83631-8
[(1S,4aR,4bR,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-1-yl]methanol 40469757 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)CO 288.50 unknown https://doi.org/10.1016/0031-9422(92)83631-8
1,1,4a-Trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol 432946 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O 302.50 unknown https://doi.org/10.1016/0031-9422(92)83631-8
https://doi.org/10.1002/PTR.2650060508
1,4a-Dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carbaldehyde 527027 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O 286.50 unknown https://doi.org/10.1016/0031-9422(92)83631-8
1,4a-Dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 90895 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0031-9422(92)83631-8
2-acetyloxy-1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 78190263 Click to see CC(=O)OC1CCC2(C(C1(C)C(=O)O)CCC(=C)C2CCC(=C)C=C)C 360.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
2-Acetyloxy-1,4a,6-trimethyl-5-(3-methylidenepent-4-enyl)-2,3,4,5,6,7,8,8a-octahydronaphthalene-1-carboxylic acid 78193139 Click to see CC1CCC2C(C1CCC(=C)C=C)(CCC(C2(C)C(=O)O)OC(=O)C)C 362.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
2,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,9,10,10a-tetrahydro-2H-phenanthren-4-one 73816007 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(C(=O)CC(C3(C)C)O)C)O 316.40 unknown https://doi.org/10.1016/0031-9422(92)83631-8
4-epi-Abietal 6427962 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O 286.50 unknown https://doi.org/10.1016/0031-9422(92)83631-8
7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 267302 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1002/PTR.2650060508
Hinokiol 12310492 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O 302.50 unknown https://doi.org/10.1016/0031-9422(92)83631-8
https://doi.org/10.1002/PTR.2650060508
Isocommunic acid 11278066 Click to see CC12CCCC(C1CCC(=C)C2CCC(=C)C=C)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
Isopimaric Acid 442048 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
Juniperexcelsic acid 490535 Click to see CC1CCC2C(C1CCC(=C)C=C)(CCC(C2(C)C(=O)O)OC(=O)C)C 362.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
Juniperexcelsis acid 478843 Click to see CC(=O)OC1CCC2(C(C1(C)C(=O)O)CCC(=C)C2CCC(=C)C=C)C 360.50 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
Sandaracopimaric Acid 221580 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1002/PTR.2650060508
https://doi.org/10.1016/S0031-9422(98)00675-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1021/NP50050A053
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697815
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697815
Sabinene 10887971 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/NP50050A053
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/NP50050A053
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1021/NP50050A053
Cyclohexene, 1-methyl-4-(1-methylethyl)- 21671 Click to see CC1=CCC(CC1)C(C)C 138.25 unknown https://doi.org/10.1021/NP50050A053
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP50050A053
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1990.9697815
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1021/NP50050A053
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/NP50050A053
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50050A053
alpha-Cubebene 442359 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50050A053
cis-beta-Guaiene 15560253 Click to see CC1CCC(=C(C)C)CC2=C1CCC2C 204.35 unknown https://doi.org/10.1021/NP50050A053
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/NP50050A053
epsilon-Muurolene 520461 Click to see CC(C)C1CCC(=C)C2C1CC(=C)CC2 204.35 unknown https://doi.org/10.1021/NP50050A053
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1R,2R,5S,7R,8R,10R)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undecane-8,10-diol 162848545 Click to see CC1CCC2C13CC(C2(C)C)C(CC3O)(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
1,7-di-epi-alpha-Cedrene 10878276 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1021/NP50050A053
2,6,6,8-Tetramethyltricyclo[5.3.1.01,5]undecane-8,10-diol 73809298 Click to see CC1CCC2C13CC(C2(C)C)C(CC3O)(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(98)00675-X
alpha-Cederene 442348 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1021/NP50050A053
beta-Cedrene 11106485 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown https://doi.org/10.1021/NP50050A053
Cedr-8(15)-ene 102432 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown https://doi.org/10.1021/NP50050A053
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown https://doi.org/10.1080/10412905.1990.9697815
https://doi.org/10.1021/NP50050A053
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,4S,5S)-5-ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexan-1-ol 14138884 Click to see CC(=C)C1CC(C(CC1(C)C=C)O)C(C)(C)O 238.37 unknown https://doi.org/10.1016/0031-9422(92)83631-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Guaiazulene 3515 Click to see CC1=C2C=CC(=C2C=C(C=C1)C(C)C)C 198.30 unknown https://doi.org/10.1021/NP50050A053
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(11S)-11-[(4-hydroxy-8,8-dimethyl-5-oxo-2-propan-2-yl-6,7-dihydrophenanthren-3-yl)oxy]-8,8-dimethyl-4-propan-2-yl-10,11-dihydro-9H-benzo[i][2]benzoxepine-1,3-dione 163035220 Click to see CC(C)C1=CC2=C(C3=C(C=C2)C(CCC3OC4=C(C=C5C=CC6=C(C5=C4O)C(=O)CCC6(C)C)C(C)C)(C)C)C(=O)OC1=O 594.70 unknown https://doi.org/10.1016/0031-9422(92)83631-8
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
[(1R,2E,8S,10R,11S)-10,11-dihydroxy-6-(methoxymethyl)-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-(hydroxymethyl)prop-2-enoate 15689665 Click to see CC12CCC(O1)(C(CC(C3=C(C(=O)OC3=C2)COC)OC(=O)C(=C)CO)(C)O)O 410.40 unknown https://doi.org/10.1016/0031-9422(92)83631-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(92)83631-8
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(92)83631-8

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