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Pinus taeda

Pinus taeda - 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 UUID64400227b6d06783736682
Scientific name Pinus taeda
Authority L.
First published in Sp. Pl. : 1000 (1753)

Description Top

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Pinus taeda, also known as loblolly pine, is a subtropical pine tree native to the Southeastern United States. It is commonly found in lowlands and swampy areas and is the second most common tree species in the US. Loblolly pine is highly valued for its timber and is considered the most commercially important tree in the Southeastern US. It was also selected as the official state tree of Arkansas. The tree can reach heights of up to 30-35 meters and has bundles of three needles that last up to two years. Its seed cones are green, ripening to a pale buff-brown color and have sharp spines. Loblolly pine is a fast-growing tree and is often found in large plantations. It is also known for its ability to withstand ice storms. Notable loblolly pines include the "Eisenhower Tree" on the 17th hole of Augusta National Golf Club and the "Morris Pine" in Arkansas. Loblolly pine also has the largest genome of any organism, with 22 billion base pairs, and was the first pine species to have its complete genome sequenced. However, it is also prone to inbreeding depression, with an average of eight lethal equivalents per haploid

Synonyms Top

Scientific name Authority First published in
Pinus lutea Walter Fl. Carol. : 237 (1788)
Pinus mughoides E.H.L.Krause Beih. Bot. Centralbl. 32(2): 330 (1914)
Pinus taeda var. mughoides E.H.L.Krause Beih. Bot. Centralbl. 32(2): 330 (1914)
Pinus taeda var. alopecuroidea Aiton Hort. Kew. 3: 368. 1789
Pinus taeda var. tenuifolia Aiton Hort. Kew. 3: 368. 1789

Common names Top

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Language Common/alternative name
English southern pine
English loblolly pine
Bulgarian тамянов бор
Czech borovice kadidlová
German weihrauch-kiefer
Esperanto torĉpino
Estonian tõrvikumänd
Persian کاج کندر
Finnish loblollymänty
Hebrew אורן קרוליינה
Japanese テーダマツ
Korean 테다소나무
Lithuanian terpentininė pušis
Norwegian Bokmål virakfuru
Polish sosna taeda
Russian Сосна ладанная
Swedish loblollytall
Chinese 火炬松

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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No subvariety added yet.

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
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Oklahoma
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000481652
UNII 776S483WWJ
Florida Plant Atlas 3526
Flora of Alabama 216
USDA Plants PITA
Tropicos 24900221
INPN 446381
KEW urn:lsid:ipni.org:names:263357-1
The Plant List kew-2562300
Missouri Botanical Garden 285006
Open Tree Of Life 1075736
Observations.org 146948
NCBI Taxonomy 3352
Nature Serve 2.155267
IUCN Red List 42420
IPNI 263357-1
iNaturalist 59921
GBIF 5285241
Freebase /m/0285xz
FEIS plants/tree/pintae
EPPO PIUTD
EOL 1033636
US Library of Congress sh85077898
USDA GRIN 28556
Wikipedia Pinus_taeda
PaleoBotany 102350

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_000404065.3 Ptaeda2.0 Scaffold TreeGenes Database 2017-01-09 N/A 20.59 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
Climate change could negate U.S. forest ecosystem service benefits gained through reductions in nitrogen and sulfur deposition Phelan JN, Van Houtven G, Clark CM, Buckley J, Cajka J, Hargrave A, Horn K, Thomas RQ, Sabo RD Sci Rep 10-May-2024
PMCID:PMC11087459
doi:10.1038/s41598-024-60652-z
PMID:38730011
Effects of Eucalyptus wood and leaf litter on saproxylic insects in the southeastern United States Ulyshen MD, Horn S, Aubrey D, Hoebeke ER, Coyle DR Sci Rep 09-May-2024
PMCID:PMC11082169
doi:10.1038/s41598-024-61193-1
PMID:38724571
Strategies, Achievements, and Potential Challenges of Plant and Microbial Chassis in the Biosynthesis of Plant Secondary Metabolites Han T, Miao G Molecules 02-May-2024
PMCID:PMC11085123
doi:10.3390/molecules29092106
PMID:38731602
Under Stress: Searching for Genes Involved in the Response of Abies pinsapo Boiss to Climate Change Blanca-Reyes I, Lechuga V, Llebrés MT, Carreira JA, Ávila C, Cánovas FM, Castro-Rodríguez V Int J Mol Sci 28-Apr-2024
PMCID:PMC11084517
doi:10.3390/ijms25094820
PMID:38732040
The complete chloroplast genome of Keteleeria evelyniana Mast var. pendula Hsüeh (Pinaceae), a species with extremely small populations in China Yang GS, Qiu Y, Yang ZA Mitochondrial DNA B Resour 26-Apr-2024
PMCID:PMC11057466
doi:10.1080/23802359.2024.2345780
PMID:38686317
Male mating season range expansion results from an increase in scale of daily movements for a polygynous–promiscuous bird Lott H, Ulrey EE, Kilgo JC, Collier BA, Chamberlain MJ, Byrne ME Ecol Evol 25-Apr-2024
PMCID:PMC11046083
doi:10.1002/ece3.11302
PMID:38681182
What drives wild pig (Sus scrofa) movement in bottomland and upland forests? Evans TS, Ellison N, Boudreau MR, Strickland BK, Street GM, Iglay RB Mov Ecol 25-Apr-2024
PMCID:PMC11044336
doi:10.1186/s40462-024-00472-y
PMID:38664784
Impacts of Invasive Plants on Native Vegetation Communities in Wetland and Stream Mitigation DeBerry DA, Hunter DM Biology (Basel) 18-Apr-2024
PMCID:PMC11048567
doi:10.3390/biology13040275
PMID:38666887
Functional Characterization of PmDXR, a Critical Rate-Limiting Enzyme, for Turpentine Biosynthesis in Masson Pine (Pinus massoniana Lamb.) Li R, Zhu L, Chen P, Chen Y, Hao Q, Zhu P, Ji K Int J Mol Sci 17-Apr-2024
PMCID:PMC11050515
doi:10.3390/ijms25084415
PMID:38673998
Genome-wide characterization of post-transcriptional processes related to wood formation in Dalbergia odorifera Jiao N, Xu J, Wang Y, Li D, Chen F, Chen Y, Chen J BMC Genomics 16-Apr-2024
PMCID:PMC11022335
doi:10.1186/s12864-024-10300-7
PMID:38627613
Large-scale analysis of the ARF and Aux/IAA gene families in 406 horticultural and other plants Feng S, Li N, Chen H, Liu Z, Li C, Zhou R, Zhang Y, Cao R, Ma X, Song X Mol Hortic 09-Apr-2024
PMCID:PMC11003162
doi:10.1186/s43897-024-00090-7
PMID:38589963
Decrypting Molecular Mechanisms Involved in Counteracting Copper and Nickel Toxicity in Jack Pine (Pinus banksiana) Based on Transcriptomic Analysis Moy A, Nkongolo K Plants (Basel) 08-Apr-2024
PMCID:PMC11013723
doi:10.3390/plants13071042
PMID:38611570
Globe-LFMC 2.0, an enhanced and updated dataset for live fuel moisture content research Yebra M, Scortechini G, Adeline K, Aktepe N, Almoustafa T, Bar-Massada A, Beget ME, Boer M, Bradstock R, Brown T, Castro FX, Chen R, Chuvieco E, Danson M, Değirmenci CÜ, Delgado-Dávila R, Dennison P, Di Bella C, Domenech O, Féret JB, Forsyth G, Gabriel E, Gagkas Z, Gharbi F, Granda E, Griebel A, He B, Jolly M, Kotzur I, Kraaij T, Kristina A, Kütküt P, Limousin JM, Martín MP, Monteiro AT, Morais M, Moreira B, Mouillot F, Msweli S, Nolan RH, Pellizzaro G, Qi Y, Quan X, Resco de Dios V, Roberts D, Tavşanoğlu Ç, Taylor AF, Taylor J, Tüfekcioğlu İ, Ventura A, Younes Cardenas N Sci Data 04-Apr-2024
PMCID:PMC10995118
doi:10.1038/s41597-024-03159-6
PMID:38575621
Complete organelle genomes of Korean fir, Abies koreana and phylogenomics of the gymnosperm genus Abies using nuclear and cytoplasmic DNA sequence data Park S, Kwak M, Park S Sci Rep 01-Apr-2024
PMCID:PMC10985005
doi:10.1038/s41598-024-58253-x
PMID:38561351
Biosynthesis Progress of High-Energy-Density Liquid Fuels Derived from Terpenes Liu J, Lin M, Han P, Yao G, Jiang H Microorganisms 30-Mar-2024
PMCID:PMC11052473
doi:10.3390/microorganisms12040706
PMID:38674649

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[(E)-3-[4-acetyloxy-3-(2-acetyloxy-5-formyl-3-methoxyphenyl)-5-methoxyphenyl]prop-2-enyl] acetate 101932969 Click to see CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC(=O)C)C2=C(C(=CC(=C2)C=O)OC)OC(=O)C 456.40 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[4-Acetyloxy-3-(2-acetyloxy-5-formyl-3-methoxyphenyl)-5-methoxyphenyl]prop-2-enyl acetate 163026426 Click to see CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC(=O)C)C2=C(C(=CC(=C2)C=O)OC)OC(=O)C 456.40 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
[(E)-3-[4-[2-acetyloxy-5-[(E)-3-acetyloxyprop-1-enyl]-3-methoxyphenoxy]-3-methoxyphenyl]prop-2-enyl] acetate 101932978 Click to see CC(=O)OCC=CC1=CC(=C(C=C1)OC2=CC(=CC(=C2OC(=O)C)OC)C=CCOC(=O)C)OC 484.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[4-[2-Acetyloxy-5-(3-acetyloxyprop-1-enyl)-3-methoxyphenoxy]-3-methoxyphenyl]prop-2-enyl acetate 162915010 Click to see CC(=O)OCC=CC1=CC(=C(C=C1)OC2=CC(=CC(=C2OC(=O)C)OC)C=CCOC(=O)C)OC 484.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
> Benzenoids / Phenols / Methoxyphenols
Coniferyl Alcohol 1549095 Click to see COC1=C(C=CC(=C1)C=CCO)O 180.20 unknown https://doi.org/10.1006/BBRC.1999.1097
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
[(2R,3S)-4-acetyloxy-2,3-bis[(4-acetyloxy-3-methoxyphenyl)methyl]butyl] acetate 101932966 Click to see CC(=O)OCC(CC1=CC(=C(C=C1)OC(=O)C)OC)C(CC2=CC(=C(C=C2)OC(=O)C)OC)COC(=O)C 530.60 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[4-Acetyloxy-2,3-bis[(4-acetyloxy-3-methoxyphenyl)methyl]butyl] acetate 14521048 Click to see CC(=O)OCC(CC1=CC(=C(C=C1)OC(=O)C)OC)C(CC2=CC(=C(C=C2)OC(=O)C)OC)COC(=O)C 530.60 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Dodecyltetradecanoic acid 14703945 Click to see CCCCCCCCCCCCC(CCCCCCCCCCCC)C(=O)O 396.70 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl thioesters / Acyl CoAs / 3-oxo-acyl CoAs
3-oxo-5,6-dehydrosuberyl-CoA 139031573 Click to see CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSC(=O)CC(=O)CC=CCC(=O)O)O 935.70 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,4bS,7R,10aR)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 12311181 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(97)01045-5
(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 10017708 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid 15618 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
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(97)01045-5
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
delta8(14)-Pimaric acid 10116 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
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(97)01045-5
Pimaric acid 220338 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1006/ABBI.1999.1467
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1006/ABBI.1999.1467
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(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-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
gamma-Glutamylmethionine sulfoximine 139584790 Click to see CS(=N)(=O)CCC(C(=O)O)NC(=O)CCC(C(=O)O)N 309.34 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(E)-3-[(3S,4R)-4-acetyloxy-5-[2-acetyloxy-5-[(2S,3R)-4-acetyloxy-3-[(4-acetyloxy-3-methoxyphenyl)methyl]-2-(acetyloxymethyl)butyl]-3-methoxyphenyl]-3-methoxycyclohexa-1,5-dien-1-yl]prop-2-enyl] acetate 163189788 Click to see CC(=O)OCC=CC1=CC(C(C(=C1)C2=C(C(=CC(=C2)CC(COC(=O)C)C(CC3=CC(=C(C=C3)OC(=O)C)OC)COC(=O)C)OC)OC(=O)C)OC(=O)C)OC 794.80 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[4-Acetyloxy-5-[2-acetyloxy-5-[4-acetyloxy-3-[(4-acetyloxy-3-methoxyphenyl)methyl]-2-(acetyloxymethyl)butyl]-3-methoxyphenyl]-3-methoxycyclohexa-1,5-dien-1-yl]prop-2-enyl acetate 162928390 Click to see CC(=O)OCC=CC1=CC(C(C(=C1)C2=C(C(=CC(=C2)CC(COC(=O)C)C(CC3=CC(=C(C=C3)OC(=O)C)OC)COC(=O)C)OC)OC(=O)C)OC(=O)C)OC 794.80 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(E)-3-[4-[(1R)-2-acetyloxy-1-[(1R,3R,4R,6S,7S)-7-acetyloxy-3-[(3R,4R)-4-acetyloxy-3-methoxycyclohexa-1,5-dien-1-yl]-4-(acetyloxymethyl)-6-methoxy-3,4,6,7-tetrahydro-1H-isochromen-1-yl]ethoxy]-3-methoxyphenyl]prop-2-enyl] acetate 163187142 Click to see CC(=O)OCC=CC1=CC(=C(C=C1)OC(COC(=O)C)C2C3=CC(C(C=C3C(C(O2)C4=CC(C(C=C4)OC(=O)C)OC)COC(=O)C)OC)OC(=O)C)OC 768.80 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[(E)-3-[4-[(1S)-2-acetyloxy-1-[(1R,3R,4S,6S,7S)-7-acetyloxy-3-[(3R,4R)-4-acetyloxy-3-methoxycyclohexa-1,5-dien-1-yl]-4-(acetyloxymethyl)-6-methoxy-3,4,6,7-tetrahydro-1H-isochromen-1-yl]ethoxy]-3-methoxyphenyl]prop-2-enyl] acetate 163189507 Click to see CC(=O)OCC=CC1=CC(=C(C=C1)OC(COC(=O)C)C2C3=CC(C(C=C3C(C(O2)C4=CC(C(C=C4)OC(=O)C)OC)COC(=O)C)OC)OC(=O)C)OC 768.80 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[(E)-3-[4-acetyloxy-3-[(1R,2S)-1,3-diacetyloxy-1-(4-acetyloxy-3-methoxyphenyl)propan-2-yl]-5-methoxyphenyl]prop-2-enyl] acetate 163195406 Click to see CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC(=O)C)C(COC(=O)C)C(C2=CC(=C(C=C2)OC(=O)C)OC)OC(=O)C 586.60 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[4-[2-acetyloxy-1-[7-acetyloxy-3-(4-acetyloxy-3-methoxycyclohexa-1,5-dien-1-yl)-4-(acetyloxymethyl)-6-methoxy-3,4,6,7-tetrahydro-1H-isochromen-1-yl]ethoxy]-3-methoxyphenyl]prop-2-enyl acetate 162907244 Click to see CC(=O)OCC=CC1=CC(=C(C=C1)OC(COC(=O)C)C2C3=CC(C(C=C3C(C(O2)C4=CC(C(C=C4)OC(=O)C)OC)COC(=O)C)OC)OC(=O)C)OC 768.80 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[4-Acetyloxy-3-[1,3-diacetyloxy-1-(4-acetyloxy-3-methoxyphenyl)propan-2-yl]-5-methoxyphenyl]prop-2-enyl acetate 163037959 Click to see CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC(=O)C)C(COC(=O)C)C(C2=CC(=C(C=C2)OC(=O)C)OC)OC(=O)C 586.60 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[2-(4-Acetyloxy-3-methoxyphenyl)-5-formyl-7-methoxy-1-benzofuran-3-yl]methyl acetate 101932972 Click to see CC(=O)OCC1=C(OC2=C1C=C(C=C2OC)C=O)C3=CC(=C(C=C3)OC(=O)C)OC 412.40 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[4-(5-Formyl-7-methoxy-3-methyl-1-benzofuran-2-yl)-2-methoxyphenyl] acetate 101932970 Click to see CC1=C(OC2=C1C=C(C=C2OC)C=O)C3=CC(=C(C=C3)OC(=O)C)OC 354.40 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[4-(5-Formyl-7-methoxy-3-methyl-1-benzofuran-2-yl)phenyl] acetate 101932971 Click to see CC1=C(OC2=C1C=C(C=C2OC)C=O)C3=CC=C(C=C3)OC(=O)C 324.30 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1006/BBRC.1999.1097
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 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/10.1021/JF60228A061
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
(8S,8aR,12aS)-2-(2,4-dihydroxyphenyl)-8-[2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-3-(3-methylbut-2-enyl)-4-oxochromen-8-yl]-5-hydroxy-9,9,11-trimethyl-3-(3-methylbut-2-enyl)-8,8a,10,12a-tetrahydroisochromeno[3,4-h]chromen-4-one 163043921 Click to see CC1=CC2C(C(OC3=C2C4=C(C(=C3)O)C(=O)C(=C(O4)C5=C(C=C(C=C5)O)O)CC=C(C)C)C6=C(C=C(C7=C6OC(=C(C7=O)CC=C(C)C)C8=C(C=C(C=C8)O)O)O)O)C(C1)(C)C 840.90 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
> Phenylpropanoids and polyketides / Stilbenes
[(2R)-2-(4-acetyloxy-3-methoxyphenyl)-3-(4-acetyloxyphenyl)propyl] acetate 162860711 Click to see CC(=O)OCC(CC1=CC=C(C=C1)OC(=O)C)C2=CC(=C(C=C2)OC(=O)C)OC 400.40 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[(2S)-2,3-bis(4-acetyloxy-3-methoxyphenyl)propyl] acetate 162916381 Click to see CC(=O)OCC(CC1=CC(=C(C=C1)OC(=O)C)OC)C2=CC(=C(C=C2)OC(=O)C)OC 430.40 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[(E)-3-[4-acetyloxy-3-[(2S)-1-acetyloxy-3-(4-acetyloxy-3-methoxyphenyl)propan-2-yl]-5-methoxyphenyl]prop-2-enyl] acetate 163188893 Click to see CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC(=O)C)C(CC2=CC(=C(C=C2)OC(=O)C)OC)COC(=O)C 528.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[(E)-3-[4-acetyloxy-3-[(Z)-1-(4-acetyloxy-3-methoxyphenyl)prop-1-en-2-yl]-5-methoxyphenyl]prop-2-enyl] acetate 101932975 Click to see CC(=CC1=CC(=C(C=C1)OC(=O)C)OC)C2=C(C(=CC(=C2)C=CCOC(=O)C)OC)OC(=O)C 468.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[(E)-3-[5-acetyloxy-2-[3-(4-acetyloxy-3-methoxyphenyl)prop-1-en-2-yl]-4-methoxyphenyl]prop-2-enyl] acetate 100935405 Click to see CC(=O)OCC=CC1=CC(=C(C=C1C(=C)CC2=CC(=C(C=C2)OC(=O)C)OC)OC)OC(=O)C 468.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
[2-(4-Acetyloxy-3-methoxyphenyl)-3-(4-acetyloxyphenyl)propyl] acetate 101932964 Click to see CC(=O)OCC(CC1=CC=C(C=C1)OC(=O)C)C2=CC(=C(C=C2)OC(=O)C)OC 400.40 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
2,3-Bis(4-acetyloxy-3-methoxyphenyl)propyl acetate 101932963 Click to see CC(=O)OCC(CC1=CC(=C(C=C1)OC(=O)C)OC)C2=CC(=C(C=C2)OC(=O)C)OC 430.40 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[4-Acetyloxy-3-[1-(4-acetyloxy-3-methoxyphenyl)prop-1-en-2-yl]-5-methoxyphenyl]prop-2-enyl acetate 162946721 Click to see CC(=CC1=CC(=C(C=C1)OC(=O)C)OC)C2=C(C(=CC(=C2)C=CCOC(=O)C)OC)OC(=O)C 468.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[4-Acetyloxy-3-[1-acetyloxy-3-(4-acetyloxy-3-methoxyphenyl)propan-2-yl]-5-methoxyphenyl]prop-2-enyl acetate 162975071 Click to see CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC(=O)C)C(CC2=CC(=C(C=C2)OC(=O)C)OC)COC(=O)C 528.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[5-Acetyloxy-2-[1-(4-acetyloxy-3-methoxyphenyl)prop-1-en-2-yl]-4-methoxyphenyl]prop-2-enyl acetate 163034376 Click to see CC(=CC1=CC(=C(C=C1)OC(=O)C)OC)C2=CC(=C(C=C2C=CCOC(=O)C)OC(=O)C)OC 468.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[5-Acetyloxy-2-[3-(4-acetyloxy-3-methoxyphenyl)prop-1-en-2-yl]-4-methoxyphenyl]prop-2-enyl acetate 163045628 Click to see CC(=O)OCC=CC1=CC(=C(C=C1C(=C)CC2=CC(=C(C=C2)OC(=O)C)OC)OC)OC(=O)C 468.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-[5-Acetyloxy-2-[3-acetyloxy-1-(4-acetyloxy-3-methoxyphenyl)prop-1-en-2-yl]-4-methoxyphenyl]prop-2-enyl acetate 162853900 Click to see CC(=O)OCC=CC1=CC(=C(C=C1C(=CC2=CC(=C(C=C2)OC(=O)C)OC)COC(=O)C)OC)OC(=O)C 526.50 unknown https://doi.org/10.1016/S0031-9422(98)00572-X
3-Methoxy-5-(2-phenylethenyl)phenol 182229 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
Stilbene 11502 Click to see C1=CC=C(C=C1)C=CC2=CC=CC=C2 180.24 unknown https://doi.org/10.1016/S0031-9422(97)01045-5
trans-Stilbene 638088 Click to see C1=CC=C(C=C1)C=CC2=CC=CC=C2 180.24 unknown https://doi.org/10.1016/S0031-9422(97)01045-5

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