Alnus firma

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID6440389e85783811353451
Scientific name	Alnus firma
Authority	Siebold & Zucc.
First published in	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 230 (1846)

Description Top

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Alnus firma is a type of tree belonging to the genus Alnus and is native to Japan. It is commonly found in various regions of Japan and is known for its distinctive features and characteristics. This species of Alnus is highly valued for its wood, which is used in various industries. It is also known for its ability to thrive in different environmental conditions, making it a popular choice for landscaping and reforestation projects. Overall, Alnus firma is an important and well-known species in Japan, with many practical and aesthetic uses.

Synonyms Top

Scientific name	Authority	First published in
Alnaster firmus	(Siebold & Zucc.) Murai	Bull. Gov. Forest Exp. Sta. 154: 64 (1963)
Alnus firma subsp. hirtella	(Franch. & Sav.) C.K.Schneid.	Pl. Wilson. 2: 506. 1916 (1916)
Alnaster firmus var. hirtellus	(Franch. & Sav.) Murai	Bull. Gov. Forest Exp. Sta. 154: 64. 1963
Alnus yasha var. macrocarpa	Callier	Repert. Spec. Nov. Regni Veg. 10: 227 (1911)
Alnus yasha var. microcarpa	Callier	Repert. Spec. Nov. Regni Veg. 10: 227 (1911)
Alnus firma f. hirtella	(Franch. & Sav.) H.Ohba	Fl. Japan 2a: 28 (2006)
Alnus firma var. hirtella	Franch. & Sav.	Enum. Pl. Jap. 2: 502 (1878)
Alnus firma var. yasha	(Matsum.) H.J.P.Winkl.	Pflanzenr. IV, 61: 104. 1904
Alnus hirtella	Koidz.	Bot. Mag. (Tokyo) 27: 144 (1913)
Duschekia firma	(Siebold & Zucc.) Pouzar	Preslia 36: 339 (1964)
Alnus yasha	Matsum.	J. Coll. Sci. Imp. Univ. Tokyo 16(5): 4 (1902)

Common names Top

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Language	Common/alternative name
Icelandic	buskölur
Japanese	夜叉五倍子
Japanese	ヤシャブシ
Polish	olsza twarda
Russian	Ольха твёрдая
Chinese	硬枝桤木
Chinese	夜叉五倍子

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-temperate click to expand
- Eastern Asia
  - Japan
  - Korea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000944965
Tropicos	3600514
KEW	urn:lsid:ipni.org:names:294920-1
The Plant List	kew-6338
Open Tree Of Life	117347
NCBI Taxonomy	109059
IUCN Red List	194589
IPNI	294920-1
iNaturalist	437253
GBIF	2876489
EPPO	ALUFI
EOL	1145878
USDA GRIN	2443
Wikipedia	Alnus_firma
CMAUP	NPO4971

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

Plant-Associated Bacillus thuringiensis and Bacillus cereus: Inside Agents for Biocontrol and Genetic Recombination in Phytomicrobiome

Sorokan A, Gabdrakhmanova V, Kuramshina Z, Khairullin R, Maksimov I

Plants (Basel)

30-Nov-2023

PMCID:	PMC10707757
doi:	10.3390/plants12234037
PMID:	38068672

Metal-Catalyzed Enantioconvergent Transformations

Yus M, Nájera C, Foubelo F, Sansano JM

Chem Rev

04-Oct-2023

PMCID:	PMC10603790
doi:	10.1021/acs.chemrev.3c00059
PMID:	37793021

Microbe-Plant Interactions Targeting Metal Stress: New Dimensions for Bioremediation Applications

Saharan BS, Chaudhary T, Mandal BS, Kumar D, Kumar R, Sadh PK, Duhan JS

J Xenobiot

01-Jun-2023

PMCID:	PMC10304886
doi:	10.3390/jox13020019
PMID:	37367495

A review of the effects of environmental hazards on humans, their remediation for sustainable development, and risk assessment

Gunjyal N, Rani S, Asgari Lajayer B, Senapathi V, Astatkie T

Environ Monit Assess

01-Jun-2023

PMCID:	PMC10234584
doi:	10.1007/s10661-023-11353-z
PMID:	37264257

Radical oxygen species: an important breakthrough point for botanical drugs to regulate oxidative stress and treat the disorder of glycolipid metabolism

Luo M, Zheng Y, Tang S, Gu L, Zhu Y, Ying R, Liu Y, Ma J, Guo R, Gao P, Zhang C

Front Pharmacol

12-May-2023

PMCID:	PMC10213330
doi:	10.3389/fphar.2023.1166178
PMID:	37251336

Phytoremediation as an Effective Remedy for Removing Trace Elements from Ecosystems

Mocek-Płóciniak A, Mencel J, Zakrzewski W, Roszkowski S

Plants (Basel)

14-Apr-2023

PMCID:	PMC10141480
doi:	10.3390/plants12081653
PMID:	37111876

Antiviral and ROS scavenging potential of Carica papaya Linn and Psidium guajava leaves extract against HIV-1 infection

Jadaun P, Shah P, Harshithkumar R, Said MS, Bhoite SP, Bokuri S, Ravindran S, Mishra N, Mukherjee A

BMC Complement Med Ther

18-Mar-2023

PMCID:	PMC10024014
doi:	10.1186/s12906-023-03916-x
PMID:	36934258

Current Scenario and Future Prospects of Endophytic Microbes: Promising Candidates for Abiotic and Biotic Stress Management for Agricultural and Environmental Sustainability

Anand U, Pal T, Yadav N, Singh VK, Tripathi V, Choudhary KK, Shukla AK, Sunita K, Kumar A, Bontempi E, Ma Y, Kolton M, Singh AK

Microb Ecol

14-Mar-2023

PMCID:	PMC10497456
doi:	10.1007/s00248-023-02190-1
PMID:	36917283

Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review

Tshikhudo PP, Ntushelo K, Mudau FN

Microorganisms

10-Feb-2023

PMCID:	PMC9967847
doi:	10.3390/microorganisms11020453
PMID:	36838418

Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review

Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK

Int J Mol Sci

01-Jan-2023

PMCID:	PMC9821772
doi:	10.3390/ijms24010739
PMID:	36614181

Plant Growth-Promoting Bacteria (PGPB) integrated phytotechnology: A sustainable approach for remediation of marginal lands

Poria V, Dębiec-Andrzejewska K, Fiodor A, Lyzohub M, Ajijah N, Singh S, Pranaw K

Front Plant Sci

21-Oct-2022

PMCID:	PMC9634634
doi:	10.3389/fpls.2022.999866
PMID:	36340355

Design, Synthesis and Evaluation of Novel Derivatives of Curcuminoids with Cytotoxicity

Chen CY, Lien JC, Chen CY, Hung CC, Lin HC

Int J Mol Sci

10-Nov-2021

PMCID:	PMC8624111
doi:	10.3390/ijms222212171
PMID:	34830055

HIV-1 Protease and Reverse Transcriptase Inhibitory Activities of Curcuma aeruginosa Roxb. Rhizome Extracts and the Phytochemical Profile Analysis: In Vitro and In Silico Screening

Sillapachaiyaporn C, Rangsinth P, Nilkhet S, Moungkote N, Chuchawankul S

Pharmaceuticals (Basel)

31-Oct-2021

PMCID:	PMC8621417
doi:	10.3390/ph14111115
PMID:	34832897

Creating High-Resolution Microscopic Cross-Section Images of Hardwood Species Using Generative Adversarial Networks

Lopes DJ, Monti GF, Burgreen GW, Moulin JC, dos Santos Bobadilha G, Entsminger ED, Oliveira RF

Front Plant Sci

13-Oct-2021

PMCID:	PMC8548738
doi:	10.3389/fpls.2021.760139
PMID:	34721488

Polyphenols and their potential role to fight viral diseases: An overview

Montenegro-Landívar MF, Tapia-Quirós P, Vecino X, Reig M, Valderrama C, Granados M, Cortina JL, Saurina J

Sci Total Environ

19-Aug-2021

PMCID:	PMC8373592
doi:	10.1016/j.scitotenv.2021.149719
PMID:	34438146

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 / Prenol lipids / Terpene lactones
Moriniafungin D	145721229	Click to see CC1CCC2C1CC3(C4CC2(C3(C(=C4)C(C)C)C(=O)O)C=O)COC5C(C6(C(C(O5)C)OC)OC(C(=O)O6)CCCC(=O)OC)O	648.70	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aR,13bR)-10-hydroxy-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	54585389	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)O)C)C)CO	620.90	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Oleanolic Acid	10494	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
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin	5281647	Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O	422.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Cinnamic Acid Phenethyl Ester	7659	Click to see C1=CC=C(C=C1)CCOC(=O)C=CC2=CC=CC=C2	252.31	unknown	https://doi.org/10.1246/BCSJ.43.2223
Phenethyl cinnamate	5369459	Click to see C1=CC=C(C=C1)CCOC(=O)C=CC2=CC=CC=C2	252.31	unknown	https://doi.org/10.1246/BCSJ.43.2223
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2R,3R,4S,5S,6R)-2-[(3R)-1,7-bis(4-hydroxyphenyl)heptan-3-yl]oxy-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]oxane-3,4,5-triol	21637600	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC(CCCCC3=CC=C(C=C3)O)CCC4=CC=C(C=C4)O)O)O)O)O)(CO)O	594.60	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R)-2-[(3R)-1,7-bis(3,4-dihydroxyphenyl)heptan-3-yl]oxy-3,5-dihydroxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	54585388	Click to see C1C(C(C(C(O1)OC(CCCCC2=CC(=C(C=C2)O)O)CCC3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	626.60	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
(4E)-1,7-Bis(3,4-dihydroxyphenyl)-4-hepten-3-one; 1,7-Bis-(3,4-dihydroxyphenyl)-4-hepten-3-one; Hirsutanone	66954880	Click to see C1=CC(=C(C=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O)O	328.40	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
(E,5R)-5-hydroxy-1,7-diphenylhept-1-en-3-one	38359503	Click to see C1=CC=C(C=C1)CCC(CC(=O)C=CC2=CC=CC=C2)O	280.40	unknown	https://doi.org/10.1246/BCSJ.43.2223
(R)-5-Hydroxy-1,7-diphenyl-3-heptanone	46213118	Click to see C1=CC=C(C=C1)CCC(CC(=O)CCC2=CC=CC=C2)O	282.40	unknown	https://doi.org/10.1246/BCSJ.43.575
1,7-Bis(3,4-dihydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one	14707657	Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC(=C(C=C3)O)O)O)O)O	478.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
1,7-Bis(3,4-dihydroxyphenyl)-5-methoxyheptan-3-one	23902340	Click to see COC(CCC1=CC(=C(C=C1)O)O)CC(=O)CCC2=CC(=C(C=C2)O)O	360.40	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
1,7-Bis(4-hydroxyphenyl)hept-5-en-3-one	162869316	Click to see C1=CC(=CC=C1CCC(=O)CC=CCC2=CC=C(C=C2)O)O	296.40	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol	75168353	Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O	494.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]oxane-3,4,5-triol	74202880	Click to see C1C(C(C(C(O1)OC(CCCCC2=CC(=C(C=C2)O)O)CCC3=CC(=C(C=C3)O)O)O)O)O	464.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
2-[1,7-Bis(4-hydroxyphenyl)heptan-3-yloxy]-6-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]oxane-3,4,5-triol	73818246	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC(CCCCC3=CC=C(C=C3)O)CCC4=CC=C(C=C4)O)O)O)O)O)(CO)O	594.60	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
2-[2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]-3,5-dihydroxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	75168334	Click to see C1C(C(C(C(O1)OC(CCCCC2=CC(=C(C=C2)O)O)CCC3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	626.60	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
5-Hydroxy-1,7-diphenyl-3-heptanone	562075	Click to see C1=CC=C(C=C1)CCC(CC(=O)CCC2=CC=CC=C2)O	282.40	unknown	https://doi.org/10.1246/BCSJ.43.575
5-Hydroxy-1,7-diphenylhept-1-en-3-one	72751360	Click to see C1=CC=C(C=C1)CCC(CC(=O)C=CC2=CC=CC=C2)O	280.40	unknown	https://doi.org/10.1246/BCSJ.43.2223
7-(3,4-Dihydroxyphenyl)-1-(4-hydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one	14707655	Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC=C(C=C3)O)O)O)O	462.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
Alnuside B	11684063	Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC=C(C=C3)O)O)O)O	462.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
Hirsutanone	637394	Click to see C1=CC(=C(C=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O)O	328.40	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
Muricarpone A	11667643	Click to see COC(CCC1=CC(=C(C=C1)O)O)CC(=O)CCC2=CC(=C(C=C2)O)O	360.40	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
Oregonin	14707658	Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)O)O)CC(=O)CCC3=CC(=C(C=C3)O)O)O)O)O	478.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
Platyphyllenone	23786382	Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC=C(C=C2)O)O	296.40	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
Rubranoside A	10097263	Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O	494.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
Rubranoside B	24011643	Click to see C1C(C(C(C(O1)OC(CCCCC2=CC(=C(C=C2)O)O)CCC3=CC(=C(C=C3)O)O)O)O)O	464.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(5S)-1,7-bis(4-hydroxyphenyl)-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-3-one	54583463	Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O	476.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
(5S)-5-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1,7-bis(4-hydroxyphenyl)heptan-3-one	54582487	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC(CCC3=CC=C(C=C3)O)CC(=O)CCC4=CC=C(C=C4)O)O)O)O)O)(CO)O	608.60	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
(S)-1,7-Bis(4-hydroxyphenyl)-5-hydroxyheptan-3-one	13347313	Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)O)O	314.40	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
1,7-Bis(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-3-one	14833391	Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O	476.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
5-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1,7-bis(4-hydroxyphenyl)heptan-3-one	76152897	Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC(CCC3=CC=C(C=C3)O)CC(=O)CCC4=CC=C(C=C4)O)O)O)O)O)(CO)O	608.60	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
5-Hydroxy-1,7-bis(4-hydroxyphenyl)heptan-3-one	13347312	Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)O)O	314.40	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
Platyphylloside	9826264	Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O	476.50	unknown	https://doi.org/10.1016/J.BMCL.2011.03.074
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7-Hydroxy-5-methoxy-2-phenylchroman-4-one	4053302	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1246/BCSJ.43.2223
Alpinetin	154279	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1246/BCSJ.43.2223
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7-methoxy-2-phenylchroman-4-one	73201	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1246/BCSJ.43.2223
5-Hydroxy-7-methoxyflavanone	4101463	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1246/BCSJ.43.2223
> Phenylpropanoids and polyketides / Stilbenes
Stilbene	11502	Click to see C1=CC=C(C=C1)C=CC2=CC=CC=C2	180.24	unknown	https://doi.org/10.1246/BCSJ.43.2223
trans-Stilbene	638088	Click to see C1=CC=C(C=C1)C=CC2=CC=CC=C2	180.24	unknown	https://doi.org/10.1246/BCSJ.43.2223

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Alnus firma

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