Liquidambar orientalis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Liquidambar orientalis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Liquidambar orientalis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643ff48f41aa3850634452
Scientific name Liquidambar orientalis
Authority Mill.
First published in Gard. Dict. ed. 8 : n.º 2 (1768)

Description Top

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Synonyms Top

Scientific name Authority First published in
Liquidambar imberbis Aiton Hort. Kew. 3: 365 (1789)

Common names Top

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Language Common/alternative name
English oriental sweetgum
Arabic عنبر دماع شرقي
Arabic الميعة
Czech ambroň východní
Persian شیرینژد خاوری
Finnish idänambrapuu
Hebrew ליקווידמבר מזרחי
Norwegian Bokmål orientalsk ambratre
Polish ambrowiec wschodni
Swedish ambraträd
Turkish sığla
Turkish anadolu sığla ağacı
Vietnamese sâu đông
Chinese 苏合香
Chinese 合香
Chinese 蘇合香樹

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000364076
UNII 759QNU787E
USDA Plants LIOR2
Tropicos 50066391
Flora of Italy 9883
KEW urn:lsid:ipni.org:names:430714-1
The Plant List kew-2348980
Missouri Botanical Garden 291500
PaleoBotany 17807
Open Tree Of Life 519500
NCBI Taxonomy 63360
IUCN Red List 62556
IPNI 430714-1
iNaturalist 356068
GBIF 3152825
Freebase /m/02r59sv
EPPO LIQOR
EOL 483571
USDA GRIN 22378
Wikipedia Liquidambar_orientalis
CMAUP NPO10256

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
First Record of Comparative Plastid Genome Analysis and Phylogenetic Relationships among Corylopsis Siebold & Zucc. (Hamamelidaceae) Kim TH, Ha YH, Setoguchi H, Choi K, Kim SC, Kim HJ Genes (Basel) 20-Mar-2024
PMCID:PMC10970243
doi:10.3390/genes15030380
PMID:38540439
Effects of grafting on chemical constituents, toxicological properties, antithrombotic activity, and myocardial infarction protection of styrax secreted from the trunk of Liquidambar orientalis Mill Huang S, Cai J, Ma L, Zhang Q, Sun Y, Zhang Q, Qin L PLoS One 05-Jan-2024
PMCID:PMC10769069
doi:10.1371/journal.pone.0289894
PMID:38181063
Holarctic Species in the Pluteus podospileus Clade: Description of Six New Species and Reassessment of Old Names Ševčíková H, Malysheva EF, Antonín V, Borovička J, Dovana F, Ferisin G, Eyssartier G, Grootmyers D, Heilmann-Clausen J, Kalichman J, Kaygusuz O, Lebeuf R, Muñoz González G, Minnis AM, Russell SD, Saar I, Nielsen IB, Frøslev TG, Justo A J Fungi (Basel) 31-Aug-2023
PMCID:PMC10532425
doi:10.3390/jof9090898
PMID:37755006
Modern drug discovery using ethnobotany: A large-scale cross-cultural analysis of traditional medicine reveals common therapeutic uses Domingo-Fernández D, Gadiya Y, Mubeen S, Bollerman TJ, Healy MD, Chanana S, Sadovsky RG, Healey D, Colluru V iScience 25-Aug-2023
PMCID:PMC10494464
doi:10.1016/j.isci.2023.107729
PMID:37701812
Targeting SARS-CoV-2 Non-Structural Proteins Tam D, Lorenzo-Leal AC, Hernández LR, Bach H Int J Mol Sci 20-Aug-2023
PMCID:PMC10455537
doi:10.3390/ijms241613002
PMID:37629182
Recent Progress and Trends in the Development of Electrospun and 3D Printed Polymeric-Based Materials to Overcome Antimicrobial Resistance (AMR) Caracciolo PC, Abraham GA, Battaglia ES, Bongiovanni Abel S Pharmaceutics 16-Jul-2023
PMCID:PMC10385409
doi:10.3390/pharmaceutics15071964
PMID:37514150
Editorial: Efficacy and mechanism of herbal medicines and their functional compounds in preventing and treating cardiovascular diseases and cardiovascular disease risk factors Meng T, Zhang Y, Wang J, Leo CH, Li Z, Zhang J, Gao K, He Q Front Pharmacol 03-Jul-2023
PMCID:PMC10352117
doi:10.3389/fphar.2023.1236821
PMID:37469872
Editorial: The brain barriers in diseases of the nervous system Joukal M, Vulchanova L, Dubový P Front Cell Neurosci 17-May-2023
PMCID:PMC10230063
doi:10.3389/fncel.2023.1215651
PMID:37265582
Gastrodia elata BI.:A Comprehensive Review of Its Traditional Use, Botany, Phytochemistry, Pharmacology, and Pharmacokinetics Wu YN, Wen SH, Zhang W, Yu SS, Yang K, Liu D, Zhao CB, Sun J Evid Based Complement Alternat Med 18-Apr-2023
PMCID:PMC10129437
doi:10.1155/2023/5606021
PMID:37114145
Evidence synthesis of Chinese medicine for monkeypox: Suggestions from other contagious pox-like viral diseases Rong HG, Zhang XW, Han M, Sun X, Wu XD, Lai XZ, Shen C, Yu WJ, Fang H, Fei YT, Liu JP Front Pharmacol 13-Mar-2023
PMCID:PMC10040637
doi:10.3389/fphar.2023.1121580
PMID:36992826
Editorial: Pharmacokinetics of herbal medicines and herb-drug interactions Jia WW, Lu C, Lin G, Ge GB Front Pharmacol 13-Dec-2022
PMCID:PMC9793084
doi:10.3389/fphar.2022.1107777
PMID:36582519
Efficacy and safety of Shexiang Baoxin Pill for stable coronary artery disease: A systematic review and meta-analysis of 42 randomized controlled trials Wei J, Ma T, Zhou C, Hao P, Li B, Wang X, Yu R, Zhu M, Wang Y Front Pharmacol 14-Nov-2022
PMCID:PMC9701736
doi:10.3389/fphar.2022.1002713
PMID:36452225
Storax Attenuates Cardiac Fibrosis following Acute Myocardial Infarction in Rats via Suppression of AT1R–Ankrd1–P53 Signaling Pathway Xu Z, Lu D, Yuan J, Wang L, Wang J, Lei Z, Liu S, Wu J, Wang J, Huang L Int J Mol Sci 29-Oct-2022
PMCID:PMC9657855
doi:10.3390/ijms232113161
PMID:36361958
Evaluation of the effects of three natural products and a hemostatic agent on wound healing: an experimental study ÇELİK YILMAZ A, AYGİN D Turk J Med Sci 30-Aug-2022
PMCID:PMC10388004
doi:10.55730/1300-0144.5558
PMID:36945964
The Importance of Antioxidant Biomaterials in Human Health and Technological Innovation: A Review Pedro AC, Paniz OG, Fernandes ID, Bortolini DG, Rubio FT, Haminiuk CW, Maciel GM, Magalhães WL Antioxidants (Basel) 24-Aug-2022
PMCID:PMC9495759
doi:10.3390/antiox11091644
PMID:36139717

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
> Benzenoids / Benzene and substituted derivatives
1-Phenylethanol 7409 Click to see CC(C1=CC=CC=C1)O 122.16 unknown via CMAUP database
1,3-Diethylbenzene 8864 Click to see CCC1=CC(=CC=C1)CC 134.22 unknown via CMAUP database
3-Phenyl-1-propanol 31234 Click to see C1=CC=C(C=C1)CCCO 136.19 unknown via CMAUP database
Benzaldehyde, oxime, (Z)- 5324470 Click to see C1=CC=C(C=C1)C=NO 121.14 unknown via CMAUP database
Trimethylbenzene 10686 Click to see CC1=C(C(=CC=C1)C)C 120.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Aminobenzoic acids and derivatives / Aminobenzoic acids
2-((Carboxymethyl)amino)-4-chlorobenzoic acid 11107141 Click to see C1=CC(=C(C=C1Cl)NCC(=O)O)C(=O)O 229.62 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Styrene 7501 Click to see C=CC1=CC=CC=C1 104.15 unknown via CMAUP database
trans-beta-Methylstyrene 252325 Click to see CC=CC1=CC=CC=C1 118.18 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
1,4a,7-Trimethyl-2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthrene-1-carboxylic acid 20744630 Click to see CC1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 276.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2,3,6-Trideuterio-4-hydroxy-5-methoxybenzaldehyde 11389509 Click to see COC1=C(C=CC(=C1)C=O)O 155.17 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Cinnamyl ricinoleate 129711932 Click to see CCCCCCC(CC=CCCCCCCCC(=O)OCC=CC1=CC=CC=C1)O 414.60 unknown https://doi.org/10.1016/0027-5107(92)90067-C
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,4bS,7S)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylate 25201251 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)[O-])C)C1)C=C 301.40 unknown via CMAUP database
(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/10.1016/0027-5107(92)90067-C
(1R,4aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylate 25203731 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)[O-])C 299.40 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0027-5107(92)90067-C
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalyl propionate 61098 Click to see CCC(=O)OC(C)(CCC=C(C)C)C=C 210.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(-)-Myrtenal 1201529 Click to see CC1(C2CC=C(C1C2)C=O)C 150.22 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol 12314318 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown via CMAUP database
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 12223113 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 23308299 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
[(1R,5R)-6,6-dimethyl-2-bicyclo[3.1.1]hept-2-enyl]methanol 6973635 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown via CMAUP database
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
Myrtenal 61130 Click to see CC1(C2CC=C(C1C2)C=O)C 150.22 unknown via CMAUP database
Verbenene 6427476 Click to see CC1(C2CC1C(=C)C=C2)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown via CMAUP database
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
2-(2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde 98497 Click to see CC1=CCC(C1(C)C)CC=O 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown via CMAUP database
(+)-Longicyclene 16217633 Click to see CC1(CCCC2(C3C1C4C2(C4C3)C)C)C 204.35 unknown via CMAUP database
(+)(-)-(E)-beta-caryophyllene 14757966 Click to see CC1(CC2C1CCC(=C)CCCC2=C)C 204.35 unknown via CMAUP database
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene 5322111 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(Z)-caryophyllene 6429301 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene oxide 2 13240188 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
Longifolene 289151 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Epioleanolic acid 11869658 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Oleanonic acid 12313704 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown via CMAUP database
> Organic acids and derivatives / Carbothioic S-acids
Pentadecanethioic acid 18413781 Click to see CCCCCCCCCCCCCCC(=O)S 258.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3'-Methylacetophenone 11455 Click to see CC1=CC(=CC=C1)C(=O)C 134.17 unknown via CMAUP database
Acetophenone 7410 Click to see CC(=O)C1=CC=CC=C1 120.15 unknown via CMAUP database
Acetophenone-2',3',4',5',6'-d5 11457690 Click to see CC(=O)C1=CC=CC=C1 125.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
2-Propenoic acid, 3-phenyl-, 3-phenyl-2-propenyl ester 31224 Click to see C1=CC=C(C=C1)C=CCOC(=O)C=CC2=CC=CC=C2 264.30 unknown https://doi.org/10.1016/0027-5107(92)90067-C
Cinnamyl cinnamate 1550890 Click to see C1=CC=C(C=C1)C=CCOC(=O)C=CC2=CC=CC=C2 264.30 unknown https://doi.org/10.1016/0027-5107(92)90067-C
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/0027-5107(92)90067-C
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/0027-5107(92)90067-C
cis-Cinnamic acid 5372954 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
1-Dideuterio-3-phenylprop-2-en-1-ol 10534709 Click to see C1=CC=C(C=C1)C=CCO 136.19 unknown via CMAUP database
Cinnamyl alcohol 5315892 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Derricidin 5961410 Click to see CC(=CCOC1=CC(=C(C=C1)C(=O)C=CC2=CC=CC=C2)O)C 308.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-Phenylpropionic acid 107 Click to see C1=CC=C(C=C1)CCC(=O)O 150.17 unknown via CMAUP database

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