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Internal ID UUID68f8f9de2df2b296438362
Scientific name Polytrichum ohioense
Authority Renauld & Cardot
First published in Rev. Bryol. 12: 11. 1885.

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Synonyms Top

Scientific name Authority First published in
Polytrichum formosum subsp. ohioense (Renauld & Cardot) Giacom. Ist. Bot. Reale Univ. Reale Lab. Crittog. Pavia, Atti 4: 288 1947
Polytrichum yezoense Horik. J. Jap. Bot. 15: 365. 1939.
Polytrichastrum ohioense (Renauld & Cardot) G.L.Sm. Mem. New York Bot. Gard. 21(3): 35. 1971.
Polytrichum ohioense f. macrocapsulum Pilous Preslia 41: 137. 1969.

Common names Top

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Language Common/alternative name
English ohio polytrichum moss
Chinese 多形拟金发藓
Chinese 多形金发藓
Chinese 多形金髮蘚

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
Tropicos 35169092
The Plant List tro-35169092
Open Tree Of Life 985314
NCBI Taxonomy 752062
Nature Serve 2.125059
iNaturalist 282181
GBIF 2682939
EOL 927811
Elurikkus 281326
World Flora Online wfo-0001170203
USDA Plants POOH
Tropicos 35141701
Open Tree Of Life 3856233
iNaturalist 167289
GBIF 4280093
Freebase /m/0g5r50g

Genomes (via NCBI) Top

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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_050002035.1 ASM5000203v1 Scaffold BGI Research 2025-04-29 193 742.88 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Ohioensin-A: a novel benzonaphthoxanthenone from Polytrichum ohioense Guo Qiang Zheng, Ching Jer Chang, Thomas J. Stout, Jon Clardy, John M. Cassady American Chemical Society (ACS) 18-Mar-2005
doi:10.1021/JA00196A085
Ohioensins: novel benzonaphthoxanthenones from Polytrichum ohioense Guo Qiang Zheng, Ching Jer Chang, Thomas J. Stout, Jon Clardy, David K. Ho, John M. Cassady American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00054A019

Phytochemical Profile Top

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Name PubChem ID Canonical SMILES MW Found in Proof
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans
4,9,11-Trihydroxy-22-oxahexacyclo[10.10.2.02,7.08,24.015,23.016,21]tetracosa-2(7),3,5,8(24),9,11,16,18,20-nonaen-13-one 3533256 Click to see 372.40 unknown https://doi.org/10.1021/JA00196A085
https://doi.org/10.1021/JO00054A019
5,6,11-Trihydroxy-9-methoxy-22-oxahexacyclo[10.10.2.02,7.08,24.015,23.016,21]tetracosa-2(7),3,5,8,10,12(24),16,18,20-nonaen-13-one 85081169 Click to see COC1=C2C3=C(C(=O)CC4C3C(C5=C2C(=C(C=C5)O)O)OC6=CC=CC=C46)C(=C1)O 402.40 unknown https://doi.org/10.1021/JO00054A019
6,11-Dihydroxy-5,9-dimethoxy-22-oxahexacyclo[10.10.2.02,7.08,24.015,23.016,21]tetracosa-2(7),3,5,8,10,12(24),16,18,20-nonaen-13-one 85141316 Click to see 416.40 unknown https://doi.org/10.1021/JO00054A019
6,11-Dihydroxy-9-methoxy-22-oxahexacyclo[10.10.2.02,7.08,24.015,23.016,21]tetracosa-2(7),3,5,8,10,12(24),16,18,20-nonaen-13-one 73081572 Click to see COC1=C2C3=C(C(=O)CC4C3C(C5=C2C(=CC=C5)O)OC6=CC=CC=C46)C(=C1)O 386.40 unknown https://doi.org/10.1021/JO00054A019
6,9,11-Trihydroxy-22-oxahexacyclo[10.10.2.02,7.08,24.015,23.016,21]tetracosa-2(7),3,5,8(24),9,11,16,18,20-nonaen-13-one 85080634 Click to see C1C2C3C(C4=C(C(=CC=C4)O)C5=C3C(=C(C=C5O)O)C1=O)OC6=CC=CC=C26 372.40 unknown https://doi.org/10.1021/JO00054A019
Ohioensin A 442531 Click to see 372.40 unknown https://doi.org/10.1021/JA00196A085
https://doi.org/10.1021/JO00054A019
Ohioensin B 9976521 Click to see 372.40 unknown https://doi.org/10.1021/JO00054A019
Ohioensin C 11740841 Click to see 386.40 unknown https://doi.org/10.1021/JO00054A019
Ohioensin D 9978441 Click to see 402.40 unknown https://doi.org/10.1021/JO00054A019
Ohioensin E 10432048 Click to see 416.40 unknown https://doi.org/10.1021/JO00054A019

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