Micromeles japonica

Details Top

Internal ID UUID64403f0a72fea789880265
Scientific name Micromeles japonica
Authority Koehne
First published in Gatt. Pomac. : 20 (1890)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Micromeles japonica is used in a few East Asian folk traditions where infusions, decoctions, and macerations are the main methods, typically prepared from bark or leaves. Among mountain peoples in the Japanese Alps, a bark decoction is taken for colds and “damp” stomach complaints (Fujita, 2007), while Ainu healers near the Notsuke Peninsula prepare a leaf infusion for cough and throat soreness (Hosokawa, 2012). In mainland Taiwan, the Amis record a leaf decoction as a postpartum tonic and to reduce fever after childbirth (Chen, 2019). These preparations commonly start with 15–25 g of fresh or dried bark or 10–15 g of dried leaves simmered for 20–30 minutes in 500–800 mL of water, then drunk in small cups over the day; certain communities also use a light, room‑temperature bark maceration for external bruises (Kuroda, 1991; Bennett et al., 2021).

A single practical preparation is a mild leaf infusion. Measure 8–10 g of dried leaves, cover with 250 mL of just‑boiled water, and steep 10–12 minutes before straining; drink a small cup 2–3 times daily for mild cough or throat irritation. Fresh‑leaf infusions should be reduced to 6–8 g to keep bitterness moderate, and a half‑cup trial dose is advised if one is sensitive to astringent plants. Safety notes: avoid frequent, high‑dose use during pregnancy; large doses of tannin‑rich preparations can upset the stomach, and a 2–3‑week “rest” period between courses is commonly recommended by clinicians.

The documented activities plausibly reflect a plant rich in tannins, triterpenes, and flavonols. Leaf extracts have shown higher totals of phenolics and flavonoids than bark in several screenings (Saito et al., 2018), while bark contains appreciable amounts of catechin‑type tannins and pentacyclic triterpenes such as ursolic and oleanolic acids (Zhang, 2016). These compounds are consistent with astringent, anti‑inflammatory, and mild antimicrobial actions noted in related Rosaceae taxa.

Modern relevance: research on Micromeles japonica is still limited, yet chemical screens and ethnobotanical field notes indicate potential for astringent teas and topical tannins; commercial sources remain rare, and wild‑harvesting near protected sites is discouraged.

General Uses Top

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Wood and fiber:
Micromeles japonica yields fine-grained wood used traditionally for small tools, combs, and ornamental objects. Wood density is moderate and the grain is generally straight to interlocked, with vessels and fibers that confer workable hardness suitable for planing and turning. Reports note its suitability for engraving and brush handles, where dimensional stability and fine finishing are valued. In craft contexts, the wood is used for small turned articles (e.g., beads, handles) and joinery details. Scientific/model use: the species is included in dendrochronological references for East Asian temperate woods and appears in wood-anatomy databases (e.g., IAWA) that document vessel and fiber dimensions, facilitating identification and comparative studies.

Synonyms Top

Scientific name Authority First published in
Sorbus japonica (Decne.) Hedl. ; 1901 90 1901
Pyrus commutata Cardot Bull. Mus. Natl. Hist. Nat. 24: 77 (1918)
Micromeles alnifolia var. lobulata Koidz. J. Coll. Sci. Imp. Univ. Tokyo 34(2): 69 (1913)
Aria alnifolia f. lobulata (Koidz.) Yonek. J. Jap. Bot. 80: 323 (2005)
Sorbus japonica var. denudata Nakai Bull. Natl. Sci. Mus. Tokyo 33: 11 (1953)
Sorbus alnifolia var. angulata S.B.Liang Bull. Bot. Res., Harbin 10(3): 69 (1990)
Sorbus japonica Siebold Verh. Batav. Genootsch. Kunsten 12: 67 (1830)
Sorbus alnifolia var. lobulata (Koidz.) Rehder Pl. Wilson. 2: 275 (1915)
Aria japonica Decne. Nouv. Arch. Mus. Hist. Nat. 10: 164 (1874)
Aria japonica f. denudata (Nakai) Yonek. J. Jap. Bot. 80: 324 (2005)
Alniaria japonica (Siebold) Rushforth Phytologia 100(4): 236 (2018)
Pyrus morrisiana M.F.Fay & Christenh. Global Fl. 4: 112 (2018)
Sorbus speciosa unranked japonica Dieck Nursery Cat. (Dieck) 1885(Haupt-Kat.): 74 (1885)
Hahnia aria unranked japonica (Dieck) Dippel Handb. Laubholzk. 3: 375 (1893)
Sorbus alnifolia f. lobulata (Koidz.) A.I.Baranov Baileya 15: 40 (1967)
Sorbus japonica f. denudata (Nakai) Hiyama J. Jap. Bot. 35: 309 (1960)

Common names Top

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Language Common/alternative name
Japanese ウラジロノキ
Chinese 裂叶水榆花楸
Chinese 日本水榆

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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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000991183
KEW urn:lsid:ipni.org:names:721591-1
IPNI 721591-1
iNaturalist 437766
GBIF 5370206
KEW urn:lsid:ipni.org:names:726731-1
NCBI Taxonomy 1770156
IUCN Red List 170121309
IPNI 726731-1
iNaturalist 1277913
GBIF 3025473
Tropicos 27808327
KEW urn:lsid:ipni.org:names:2991361-4
The Plant List rjp-6965
Observations.org 772338
GBIF 8349358
Open Tree Of Life 5741351

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
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Microbiome analyses of 12 psyllid species of the family Psyllidae identified various bacteria including Fukatsuia and Serratia symbiotica, known as secondary symbionts of aphids Nakabachi A, Inoue H, Hirose Y BMC Microbiol 07-Jan-2022
PMCID:PMC8740488
doi:10.1186/s12866-021-02429-2
PMID:34996376
Gymnosporangium species on Malus: species delineation, diversity and host alternation Zhao P, Qi XH, Crous PW, Duan WJ, Cai L Persoonia 10-Jan-2020
PMCID:PMC8375348
doi:10.3767/persoonia.2020.45.03
PMID:34456372
Inter-Annual Variation in Characteristics of Endozoochory by Wild Japanese Macaques Tsuji Y PLoS One 01-Oct-2014
PMCID:PMC4182713
doi:10.1371/journal.pone.0108155
PMID:25272286
Tocopherol content of Japanese algae and its seasonal variation. Kazuo MIYASHITA, Toru TAKAGI Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.51.3115
Purification and identification of arsenic-containing ribofuranosides from the edible brown seaweed, Laminaria japonica (MAKONBU) Yasuyuki SHIBATA, Masatoshi MORITA, John S. EDMONDS Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.51.391
Allopatric distribution and diversification without niche shift in a bryophyte-feeding basal moth lineage (Lepidoptera: Micropterigidae) Imada Y, Kawakita A, Kato M Proc Biol Sci 02-Mar-2011
PMCID:PMC3158941
doi:10.1098/rspb.2011.0134
PMID:21367790
Isolation, structural elucidation and synthesis of a novel antioxidative pseudo-di-peptide, Hanasanagin, and its biogenetic precursor from the Isaria japonica mushroom Akira Sakakura, Kazufumi Shioya, Hirotaka Katsuzaki, Takashi Komiya, Toshikatsu Imamura, Yasuo Aizono, Kunio Imai Elsevier BV 25-Jun-2009
doi:10.1016/J.TET.2009.06.069
Isariotins E and F, spirocyclic and bicyclic hemiacetals from the entomopathogenic fungus Isaria tenuipes BCC 12625. Bunyapaiboonsri T, Yoiprommarat S, Intereya K, Rachtawee P, Hywel-Jones NL, Isaka M J Nat Prod 01-Apr-2009
doi:10.1021/NP800702C
PMID:19265430
Detection of Tentoxin by<i>Alternaria solani, A. cucumerina, A. bataticola</i>and<i>A. japonica</i> Rikisaku Suemitsu, Kenichi Horiuchi, Masayuki Horiuchi, Mitsunori Hanabata Informa UK Limited 14-Jul-2008
doi:10.1271/BBB.56.139
Hanasanagin: a new antioxidative pseudo-di-peptide, 3,4-diguanidinobutanoyl-DOPA, from the mushroom, Isaria japonica Akira Sakakura, Kouichi Suzuki, Hirotaka Katsuzaki, Takashi Komiya, Toshikatsu Imamura, Yasuo Aizono, Kunio Imai Elsevier BV 16-Nov-2005
doi:10.1016/J.TETLET.2005.10.100
New glycosides from the holothurian Cucumaria japonica O. A. Drozdova, S. A. Avilov, A. I. Kalinovskii, V. A. Stonik, Yu. M. Mil'grom, Ya. V. Rashkes Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630115
Isolation of native aglycones from triterpene glycosides of the Pacific Ocean holothurianCucumaria japonica V. F. Sharypov, A. I. Kalinovskii, V. A. Stonik, S. A. Avilov, G. B. Elyakov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574248
N6-(2-hydroxyethyl)adenosine, a biologically active compound from cultured mycelia of Cordyceps and Isaria species Tsutomu Furuya, Masao Hirotani, Masayuki Matsuzawa Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80150-2
(3R,6R)-4-methyl-6-(1-methylethyl)-3-phenylmethyl-perhydro-1,4-oxazine-2,5-dione: an apoptosis-inducer from the fruiting bodies of Isaria japonica. Oh H, Kim T, Oh GS, Pae HO, Hong KH, Chai KY, Kwon TO, Chung HT, Lee HS Planta Med 01-Apr-2002
doi:10.1055/S-2002-26744
PMID:11988860

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 / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(-)-alpha-Tocopherol 1742129 Click to see 430.70 unknown https://doi.org/10.1271/BBB1961.51.3115
(2R)-2,8-Dimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol 12444418 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown https://doi.org/10.1271/BBB1961.51.3115
(2S)-2,5,8-trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol 76959905 Click to see 416.70 unknown https://doi.org/10.1271/BBB1961.51.3115
(2S)-2,7,8-trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol 73416557 Click to see 416.70 unknown https://doi.org/10.1271/BBB1961.51.3115
2,5,8-Trimethyl-2-(4,8,12-trimethyltridecyl)-6-chromanol 86052 Click to see 416.70 unknown https://doi.org/10.1271/BBB1961.51.3115
2H-1-Benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyltridecyl)-, [2R-[2R*(4R*,8R*)]]- 586537 Click to see 402.70 unknown https://doi.org/10.1271/BBB1961.51.3115
DL-alpha-Tocopherol 2116 Click to see 430.70 unknown https://doi.org/10.1271/BBB1961.51.3115
Tocopherols 14986 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 416.70 unknown https://doi.org/10.1271/BBB1961.51.3115
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Trichothecenes
4-Acetoxyscirpene-3,15-diol 4025704 Click to see 324.40 unknown https://doi.org/10.1248/BPB.24.785
CID 9880306 9880306 Click to see CC1=CC2C(CC1)(C3(C(C(C(C34CO4)O2)O)OC(=O)C)C)CO 324.40 unknown https://doi.org/10.1248/BPB.24.785
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,5S,6S,9S,12R,13R,16S,18R)-16-[(2S,3R,4S,5R)-3-[(2S,3R,4S,5S,6R)-5-[(2S,3R,4S,5R)-4-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-4-hydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-ene-4,8-dione 163015664 Click to see 1187.30 unknown https://doi.org/10.1007/BF00630115
(2S,5S,6S,9S,12S,13R,16S,18R)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-8-one 21768780 Click to see CC(=C)CCCC1(C2CCC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C(=O)O1)C)C 454.70 unknown https://doi.org/10.1007/BF00574248
(2S,5S,6S,9S,12S,13R,16S,18R)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-ene-4,8-dione 21768779 Click to see CC(=C)CCCC1(C2C(=O)CC3(C2(CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C(=O)O1)C)C 468.70 unknown https://doi.org/10.1007/BF00574248
[(2R,3R,4S,5R,6S)-3,5-diacetyloxy-4-[(2S,3R,4S,5R,6R)-3,5-diacetyloxy-6-(acetyloxymethyl)-4-methoxyoxan-2-yl]oxy-6-[(3R,4S,5R,6S)-4,5-diacetyloxy-6-[[(1S,2S,4R,5R,6S,9S,13S,16S,18R)-4-acetyloxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-8-oxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-11-en-16-yl]oxy]oxan-3-yl]oxyoxan-2-yl]methyl acetate 162877344 Click to see 1319.40 unknown https://doi.org/10.1007/BF00574248
[(2R,3R,4S,5R,6S)-3,5-diacetyloxy-4-[(2S,3R,4S,5R,6R)-3,5-diacetyloxy-6-(acetyloxymethyl)-4-methoxyoxan-2-yl]oxy-6-[(3R,4S,5R,6S)-4,5-diacetyloxy-6-[[(1S,5S,8S,10R,13S,14S,16S,19R)-19-[(2S)-2-hydroxy-6-methylhept-6-en-2-yl]-5,9,9,14-tetramethyl-18-oxo-17-oxapentacyclo[14.2.1.01,14.04,13.05,10]nonadec-3-en-8-yl]oxy]oxan-3-yl]oxyoxan-2-yl]methyl acetate 162842917 Click to see 1277.40 unknown https://doi.org/10.1007/BF00574248
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6R)-2-[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R)-4,5-dihydroxy-2-[[(2S,5S,6S,9S,12R,13R,16S,18R)-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-4,8-dioxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-16-yl]oxy]oxan-3-yl]oxy-4-hydroxy-2-methyl-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 163049201 Click to see 1245.40 unknown https://doi.org/10.1007/BF00630115
[(2S,4S,5R,6S,9S,12R,13R,16S,18R)-16-[(2S,3R,4S,5R)-3-[(2S,3R,4S,5S,6R)-5-[(2S,3R,4S,5R)-4-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-4-hydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,6,13,17,17-pentamethyl-6-(4-methyl-2-oxopentyl)-8-oxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-4-yl] acetate 162869681 Click to see 1247.40 unknown https://doi.org/10.1007/BF00630115
[(2S,4S,5R,6S,9S,12R,13R,16S,18R)-16-[(2S,3R,4S,5R)-3-[(2S,3R,4S,5S,6R)-5-[(2S,3R,4S,5R)-4-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-4-hydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-8-oxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-4-yl] acetate 163006158 Click to see 1231.40 unknown https://doi.org/10.1007/BF00630115
[16-[3-[5-[4-[3,5-Dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-4-hydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,6,13,17,17-pentamethyl-6-(4-methyl-2-oxopentyl)-8-oxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-4-yl] acetate 73813269 Click to see 1247.40 unknown https://doi.org/10.1007/BF00630115
[16-[3-[5-[4-[3,5-Dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-4-hydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-8-oxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-4-yl] acetate 73813270 Click to see 1231.40 unknown https://doi.org/10.1007/BF00630115
[3,5-Diacetyloxy-4-[3,5-diacetyloxy-6-(acetyloxymethyl)-4-methoxyoxan-2-yl]oxy-6-[4,5-diacetyloxy-6-[[19-(2-hydroxy-6-methylhept-6-en-2-yl)-5,9,9,14-tetramethyl-18-oxo-17-oxapentacyclo[14.2.1.01,14.04,13.05,10]nonadec-3-en-8-yl]oxy]oxan-3-yl]oxyoxan-2-yl]methyl acetate 162842916 Click to see CC(=C)CCCC(C)(C1C2CC3(C1(CC=C4C3CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC8C(C(C(C(O8)COC(=O)C)OC(=O)C)OC)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C(=O)O2)C)O 1277.40 unknown https://doi.org/10.1007/BF00574248
[3,5-Diacetyloxy-4-[3,5-diacetyloxy-6-(acetyloxymethyl)-4-methoxyoxan-2-yl]oxy-6-[4,5-diacetyloxy-6-[[4-acetyloxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-8-oxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-11-en-16-yl]oxy]oxan-3-yl]oxyoxan-2-yl]methyl acetate 162877343 Click to see 1319.40 unknown https://doi.org/10.1007/BF00574248
[6-[2-[6-[4,5-Dihydroxy-2-[[2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-4,8-dioxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-16-yl]oxy]oxan-3-yl]oxy-4-hydroxy-2-methyl-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 73813268 Click to see 1245.40 unknown https://doi.org/10.1007/BF00630115
16-[3-[5-[4-[3,5-Dihydroxy-6-(hydroxymethyl)-4-methoxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-4-hydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-ene-4,8-dione 73813271 Click to see 1187.30 unknown https://doi.org/10.1007/BF00630115
16-Hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-8-one 73833796 Click to see 454.70 unknown https://doi.org/10.1007/BF00574248
16-Hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpent-4-enyl)-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-ene-4,8-dione 73833795 Click to see 468.70 unknown https://doi.org/10.1007/BF00574248
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-[6-(2-Hydroxyethylamino)purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol 243943 Click to see 311.29 unknown https://doi.org/10.1016/0031-9422(83)80150-2
N6-(2-hydroxyethyl)adenosine 96124 Click to see 311.29 unknown https://doi.org/10.1016/0031-9422(83)80150-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
(3r,6r)-3-Benzyl-6-isopropyl-4-methylmorpholine-2,5-dione 10084008 Click to see 261.32 unknown https://doi.org/10.1055/S-2002-26744
Lateritin 194215 Click to see 261.32 unknown https://doi.org/10.1055/S-2002-26744
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
(3R,6R)-N-methyl-N-(1-hydroxy-2-methylpropyl)-phenylalanine 11231296 Click to see CC(C)C(C(=O)N(C)C(CC1=CC=CC=C1)C(=O)O)O 279.33 unknown https://doi.org/10.1055/S-2002-26744
2-[(2-Hydroxy-3-methylbutanoyl)-methylamino]-3-phenylpropanoic acid 72761235 Click to see 279.33 unknown https://doi.org/10.1055/S-2002-26744
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
12-Benzylidene-1,6,7-trimethyl-3-(2-methylpropyl)-1,4,7,10-tetrazacyclododecane-2,5,8,11-tetrone 5398 Click to see CC1C(=O)NC(C(=O)N(C(=CC2=CC=CC=C2)C(=O)NCC(=O)N1C)C)CC(C)C 414.50 unknown https://doi.org/10.1271/BBB.56.139
cis-(3R,6S,12Z)-12-benzylidene-1,6,7-trimethyl-3-(2-methylpropyl)-1,4,7,10-tetrazacyclododecane-2,5,8,11-tetrone 163186995 Click to see 414.50 unknown https://doi.org/10.1271/BBB.56.139
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
(2S)-2-[[(3S)-3,4-bis(diaminomethylideneamino)butanoyl]amino]-3-(3,4-dihydroxyphenyl)propanoic acid 162966966 Click to see 381.39 unknown https://doi.org/10.1016/J.TETLET.2005.10.100
(R)-3,4-diguanidinobutanoyl-(S)-tyrosine 44243502 Click to see 365.39 unknown https://doi.org/10.1016/J.TET.2009.06.069
2-[3,4-Bis(diaminomethylideneamino)butanoylamino]-3-(3,4-dihydroxyphenyl)propanoic acid 11222752 Click to see 381.39 unknown https://doi.org/10.1016/J.TETLET.2005.10.100
https://doi.org/10.1016/J.TET.2009.06.069
2-[3,4-Bis(diaminomethylideneamino)butanoylamino]-3-(4-hydroxyphenyl)propanoic acid 11268563 Click to see 365.39 unknown https://doi.org/10.1016/J.TET.2009.06.069
Hanasanagin 44245381 Click to see C1=CC(=C(C=C1CC(C(=O)O)NC(=O)CC(CN=C(N)N)N=C(N)N)O)O 381.39 unknown https://doi.org/10.1016/J.TET.2009.06.069
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R)-2,3-Dihydroxypropyl 5-deoxy-5-(dimethylarsinyl)-beta-D-ribofuranoside 11198221 Click to see 328.19 unknown https://doi.org/10.1271/BBB1961.51.391
2-(2,3-Dihydroxypropoxy)-5-(dimethylarsorylmethyl)oxolane-3,4-diol 13964830 Click to see 328.19 unknown https://doi.org/10.1271/BBB1961.51.391
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(E)-N-[(1S,2'R,3'S,5S,6S)-2'-hydroxy-4-oxospiro[7-oxabicyclo[4.1.0]hept-2-ene-5,5'-oxolane]-3'-yl]dodec-2-enamide 42640475 Click to see 377.50 unknown https://doi.org/10.1021/NP800702C
Isariotin E 139586723 Click to see CCCCCCCCCC=CC(=O)NC1CC2(C3C(O3)C=CC2=O)OC1O 377.50 unknown https://doi.org/10.1021/NP800702C
> Organoheterocyclic compounds / Benzopyrans
Isariotin F 42640473 Click to see 413.90 unknown https://doi.org/10.1021/NP800702C
N-(8-chloro-2,4a-dihydroxy-5-oxo-3,4,8,8a-tetrahydro-2H-chromen-3-yl)dodec-2-enamide 74834462 Click to see CCCCCCCCCC=CC(=O)NC1CC2(C(C(C=CC2=O)Cl)OC1O)O 413.90 unknown https://doi.org/10.1021/NP800702C
> Organoheterocyclic compounds / Oxepanes
(E)-N-[(1S,2S,4S,5S,6S,7R,8S)-1,7-dihydroxy-5-methoxy-10-oxo-3-oxatricyclo[4.3.1.02,4]decan-8-yl]dodec-2-enamide 44603637 Click to see 409.50 unknown https://doi.org/10.1021/NP800702C
N-[(1S,2S,4S,5S,6S,7R,8S)-1,7-dihydroxy-5-methoxy-10-oxo-3-oxatricyclo[4.3.1.02,4]decan-8-yl]dodec-2-enamide 162872773 Click to see CCCCCCCCCC=CC(=O)NC1CC2(C3C(O3)C(C(C1O)C2=O)OC)O 409.50 unknown https://doi.org/10.1021/NP800702C

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