PlantaeDB Logo
Login Sign-up

Polypodium virginianum

Polypodium virginianum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID6440773edd719177230254
Scientific name Polypodium virginianum
Authority L.
First published in Sp. Pl. : 1085 (1753)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Polypodium vulgare var. acuminatum Gilbert Fern Bull. 10: 13 (1902)
Polypodium vulgare var. virginianum (L.) Eaton Man. Bot. 373 1818
Polypodium virginianum f. brachypteron Fernald Rhodora 24: 141 (1922)
Polypodium vulgare f. brachypteron Ridlon Amer. Fern J. 11: 122 (1922)
Polypodium vinlandicum Á.Löve & D.Löve Taxon 26: 324 (1977)
Polypodium virginianum f. acuminatum Fernald Rhodora 24: 141 (1922)
Polypodium virginianum f. alato-multifidum Fernald Rhodora 24: 142 (1922)
Polypodium virginianum f. bipinnatifidum Fernald Rhodora 24: 141 (1922)
Polypodium virginianum f. biserratum (Millsp.) M.Broun Index No. Amer. Ferns : 142 (1938)
Polypodium virginianum f. cambricoides F.W.Gray Amer. Fern J. 14: 5, pl. 2 (1924)
Polypodium virginianum f. deltoideum Fernald Rhodora 24: 141 (1922)
Polypodium virginianum f. elongatum Fernald Rhodora 24: 141 (1922)
Polypodium virginianum f. subsimplex Fernald Rhodora 24: 141 (1922)
Polypodium vulgare f. biserratum Millsp. Fl. W. Virginia : 479 (1892)
Polypodium vulgare f. deltoideum Gilbert Fern Bull. 14: 37 (1906)
Polypodium vulgare f. elongatum Jewell Maine Woods (Phillips, ME) 30(31): 1. 1908
Polypodium vulgare f. hastatum Gilbert Fern Bull. 14: 37 (1906)
Polypodium vulgare f. marginale Gilbert Fern Bull. 14: 35 (1906)
Polypodium vulgare f. rotundatum Ridlon Amer. Fern J. 11: 48, pl. 1 (1921)
Polypodium vulgare f. projectum Fernald Rhodora 24: 140 (1922)
Polypodium vulgare var. alato-multifidum Gilbert Fern Bull. 14: 105 (1906)
Polypodium vulgare var. churchiae Gilbert Fern Bull. 14: 39 (1906)
Polypodium vulgare var. deceptum Maxon Proc. U. S. Natl. Mus. 23: 628 (1901)
Polypodium vulgare var. bifido-multifidum Gilbert Fern Bull. 14: 39 (1906)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English rock polypody
Arabic سرخس فرجينياني
Chinese 假友水龙骨
Chinese 北美多足蕨
Chinese 东北多足蕨

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
pour boiling water over milled sphagnum moss, sow seeds, enclose in plastic bag

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • Labrador
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Minnesota
      • Missouri
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Georgia
      • Kentucky
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Subarctic America
      • Alaska
      • Greenland
      • Northwest Territorie
    • Western Canada
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001109259
UNII 0KP7RRB9SA
Flora of Alabama 163
Canadensys 8241
USDA Plants POVI7
Tropicos 26602421
INPN 761878
KEW urn:lsid:ipni.org:names:207762-2
The Plant List tro-26602421
Missouri Botanical Garden 285769
Open Tree Of Life 860113
NCBI Taxonomy 872808
Nature Serve 2.140260
IPNI 207762-2
iNaturalist 54411
GBIF 5274950
Freebase /m/09gg0x_
WisFlora 4598
EPPO PLVVI
EOL 597741
USDA GRIN 403331
Wikipedia Polypodium_virginianum

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
Phylotranscriptomics Illuminates the Placement of Whole Genome Duplications and Gene Retention in Ferns Pelosi JA, Kim EH, Barbazuk WB, Sessa EB Front Plant Sci 14-Jul-2022
PMCID:PMC9330400
doi:10.3389/fpls.2022.882441
PMID:35909764
Genome size evolution of the extant lycophytes and ferns Wang FG, Wang AH, Bai CK, Jin DM, Nie LY, Harris A, Che L, Wang JJ, Li SY, Xu L, Shen H, Gu YF, Shang H, Duan L, Zhang XC, Chen HF, Yan YH Plant Divers 01-Jan-2022
PMCID:PMC9043363
doi:10.1016/j.pld.2021.11.007
PMID:35505989
Floristic Changes in the Understory Vegetation of Mixed Temperate New England Freshwater Island Forests over a Period of 33 Years Holland MM, Winkler M Plants (Basel) 18-Nov-2020
PMCID:PMC7698944
doi:10.3390/plants9111600
PMID:33218069
Origins and Evolution of Cuticle Biosynthetic Machinery in Land Plants Kong L, Liu Y, Zhi P, Wang X, Xu B, Gong Z, Chang C Plant Physiol 15-Sep-2020
PMCID:PMC7723097
doi:10.1104/pp.20.00913
PMID:32934149
Fifteen microsatellite markers for the Appalachian rockcap fern, Polypodium appalachianum (Polypodiaceae), and its relatives Kasireddy V, Mitchell E, Murrell ZE, Gillespie EL Appl Plant Sci 08-Nov-2018
PMCID:PMC6240454
doi:10.1002/aps3.1195
PMID:30473941
A review of the use of pteridophytes for treating human ailments Baskaran XR, Geo Vigila AV, Zhang SZ, Feng SX, Liao WB J Zhejiang Univ Sci B 01-Feb-2018
PMCID:PMC5833325
doi:10.1631/jzus.B1600344
PMID:29405039
Ecdysteroid-containing food supplements from Cyanotis arachnoidea on the European market: evidence for spinach product counterfeiting Hunyadi A, Herke I, Lengyel K, Báthori M, Kele Z, Simon A, Tóth G, Szendrei K Sci Rep 08-Dec-2016
PMCID:PMC5144001
doi:10.1038/srep37322
PMID:27929032
The Epiphytic Fern Elaphoglossum luridum (Fée) Christ. (Dryopteridaceae) from Central and South America: Morphological and Physiological Responses to Water Stress Minardi BD, Voytena AP, Santos M, Randi ÁM ScientificWorldJournal 20-Oct-2014
PMCID:PMC4217239
doi:10.1155/2014/817892
PMID:25386618
Beyond a Climate-Centric View of Plant Distribution: Edaphic Variables Add Value to Distribution Models Beauregard F, de Blois S PLoS One 21-Mar-2014
PMCID:PMC3962442
doi:10.1371/journal.pone.0092642
PMID:24658097
Leaf Area and Water Content Changes after Permanent and Temporary Storage Juneau KJ, Tarasoff CS PLoS One 03-Aug-2012
PMCID:PMC3411807
doi:10.1371/journal.pone.0042604
PMID:22880051
Fern constituents: Cyclopodmenyl acetate, a cycloartanoid having a new 33-carbon skeleton, isolated from Polypodium vulgare. Yoko ARAI, Kenji SHIOJIMA, Hiroyuki AGETA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.37.560
Phytoecdysteroid overproduction in Polypodium vulgare prothalli Natàlia Reixach, Josep Irurre-Santillari, Francisco Camps, Enric Melé, Joaquima Messeguer, Josefina Casas Elsevier BV 23-Jul-2008
doi:10.1016/S0031-9422(97)80008-8
Reproductive and Competitive Interactions Among Gametophytes of the Allotetraploid Fern Dryopteris corleyi and its Two Diploid Parents Jiménez A, Quintanilla LG, Pajarón S, Pangua E Ann Bot 21-Jun-2008
PMCID:PMC2701796
doi:10.1093/aob/mcn099
PMID:18567915
Natural high‐intensity sweeteners K. J. PARKER Wiley 26-Oct-2007
doi:10.1111/J.1467-3010.1976.TB00781.X
Synthesis and Structure Revision of Intensely Sweet Saponin Osladin Hidetoshi Yamada, Mugio Nishizawa American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00107A018

Phytochemical Profile Top

Add a new one!
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
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3S,3aR,5aR,5bR,7aS,11aS,11bR,13aS,13bS)-5a,5b,8,8,11a,13b-hexamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene 162948991 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
[(2S)-2-[(3S,3aR,5aR,5bR,7aS,11aS,11bR,13aS,13bS)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]propyl] acetate 162958194 Click to see CC(COC(=O)C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 470.80 unknown https://doi.org/10.1016/0031-9422(91)83212-4
2-(5a,5b,8,8,11a,13b-Hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl)propan-2-ol 5245211 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
2-(5a,5b,8,8,11a,13b-Hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl)propyl acetate 4481464 Click to see CC(COC(=O)C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 470.80 unknown https://doi.org/10.1016/0031-9422(91)83212-4
2-[(3R,3aS,5aR,5bR,7aR,11aS,11bR,13aS,13bS)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl]propan-2-ol 162881811 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)C)C 428.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
5a,5b,8,8,11a,13b-Hexamethyl-3-propan-2-yl-1,2,4,5,6,7,7a,9,10,11,11b,12,13,13a-tetradecahydrocyclopenta[a]chrysene 12310611 Click to see CC(C)C1=C2CCC3(C(C2(CC1)C)CCC4C3(CCC5C4(CCCC5(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
Hopene b 605866 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(6S,7Ar)-2-[(2E,4E,6E,8E,10E,12E,14E,16E)-17-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-6,11,15-trimethylheptadeca-2,4,6,8,10,12,14,16-octaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 134737870 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CC(CC3(O2)C)O)(C)C)C)C 584.90 unknown https://doi.org/10.1016/0305-1978(85)90030-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,5S,7S,10R,11R,14R,15S,20R)-1,2,11,15,19,19-hexamethyl-7-propan-2-yl-6-oxahexacyclo[12.8.0.02,11.05,7.05,10.015,20]docosane 162895786 Click to see CC(C)C12CCC3C1(O2)CCC4(C3(CCC5C4(CCC6C5(CCCC6(C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0040-4039(00)76262-9
(3R,3aR,5aS,7aS,11aS,11bR,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,7,7a,9,10,11,11b,12,13,13b-tetradecahydrocyclopenta[a]chrysene 13857703 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4C3=CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.37.560
(4aS,8S,8aS)-4,4,8a-trimethyl-7-methylidene-8-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-2,3,4a,5,6,8-hexahydro-1H-naphthalene 11304437 Click to see CC(=CCCC(=CCCC(=CCCC1C(=C)CCC2C1(CCCC2(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
3a,5a,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,5b,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysene 4481463 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
4,4,8,10,14-pentamethyl-17-(6-methylhepta-1,5-dien-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 73194675 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCCC4(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
4,4,8a-trimethyl-7-methylidene-8-(4,8,12-trimethyltrideca-3,7,11-trienyl)-2,3,4a,5,6,8-hexahydro-1H-naphthalene 72791841 Click to see CC(=CCCC(=CCCC(=CCCC1C(=C)CCC2C1(CCCC2(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
Dammara-20,24-diene 15432633 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCCC4(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
Fernene 441679 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.37.560
Serraten 605865 Click to see CC1(CCCC2(C1CCC3(C2CCC4C(=CCC5C4(CCCC5(C)C)C)C3)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(3R,3aR,5aS,5bR,7aR,11aS,11bR)-3a,5a,5b,8,8,11a-hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13-tetradecahydrocyclopenta[a]chrysene 162995590 Click to see CC(C)C1CCC2=C3CCC4C5(CCCC(C5CCC4(C3(CCC12C)C)C)(C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
3a,5a,5b,8,8,11a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13-tetradecahydrocyclopenta[a]chrysene 12310615 Click to see CC(C)C1CCC2=C3CCC4C5(CCCC(C5CCC4(C3(CCC12C)C)C)(C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
Hopene II 12310619 Click to see CC(C)C1CCC2=C3CCC4C5(CCCC(C5CCC4(C3(CCC12C)C)C)(C)C)C 410.70 unknown https://doi.org/10.1248/CPB.37.560
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R,5S)-2,3,5,6-tetrahydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 11016518 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(C(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1016/S0040-4020(01)85247-9
https://doi.org/10.1016/0031-9422(96)00336-6
(2S,3R,5S,9R,10R,13R,14S,17S)-2,3,5,14-tetrahydroxy-10,13-dimethyl-17-[(2R,3R,5S)-2,3,5,6-tetrahydroxy-6-methylheptan-2-yl]-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one 102004055 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CC(C(C)(C)O)O)O)O)O 512.60 unknown https://doi.org/10.1016/S0040-4020(01)85247-9
(2S,3S,5R,9R,10S,13S,14S,17R)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2S,3S,6S)-2,3,7-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 91900472 Click to see CC(CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)CO 480.60 unknown https://doi.org/10.1016/S0040-4020(01)85247-9
https://doi.org/10.1016/S0031-9422(97)80008-8
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,5,6-tetrahydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 73744749 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(C(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1016/S0031-9422(97)80008-8
https://doi.org/10.1016/S0040-4020(01)85247-9
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,7-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 119238 Click to see CC(CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)CO 480.60 unknown https://doi.org/10.1016/S0040-4020(01)85247-9
https://doi.org/10.1016/S0031-9422(97)80008-8
2,3,5,14-Tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one 271604 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://doi.org/10.1016/S0040-4039(00)70794-5
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1016/0031-9422(96)00336-6
https://doi.org/10.1016/0031-9422(90)85339-H
https://doi.org/10.1016/S0021-9673(01)89391-2
24-Hydroxyecdysone 129699851 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CC(C(C)(C)O)O)O 480.60 unknown https://doi.org/10.1016/S0040-4020(01)85247-9
https://doi.org/10.1016/S0031-9422(97)80008-8
24-Hydroxyecdysone 102004056 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CC(C(C)(C)O)O)O 480.60 unknown https://doi.org/10.1016/S0040-4020(01)85247-9
25S-Inokosterone 12358616 Click to see CC(CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)CO 480.60 unknown https://doi.org/10.1016/S0031-9422(97)80008-8
2beta,3beta,5beta,14,20,22R,25-Heptahydroxycholest-7-en-6-one 441833 Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 496.60 unknown https://doi.org/10.1016/S0021-9673(01)89391-2
https://doi.org/10.1016/S0031-9422(97)80008-8
https://doi.org/10.1016/0021-9673(93)83461-Z
Inokosterone 441828 Click to see CC(CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)CO 480.60 unknown https://doi.org/10.1016/S0031-9422(97)80008-8
https://doi.org/10.1016/0031-9422(96)00336-6
Pterosterone 441836 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O 480.60 unknown https://doi.org/10.1016/0031-9422(96)00336-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
Ecdysone 19212 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O 464.60 unknown https://doi.org/10.1016/S0031-9422(97)80008-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
[(3S,8R,9S,13R)-9-ethyl-4,4,13,14-tetramethyl-17-(6-methylheptan-2-yl)-2,3,5,6,7,8,10,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 5316234 Click to see CCC12CCC3(C(CCC3(C1CCC4C2CCC(C4(C)C)OC(=O)C)C)C(C)CCCC(C)C)C 486.80 unknown https://doi.org/10.1248/CPB.37.560
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1S,3R,6S,7S,8R,11R,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 162993292 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1OC(=O)C)C)C(C)CCCC(C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
[(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R)-5,5-dimethyl-6-methylideneoctan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 21629931 Click to see CCC(=C)C(C)(C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 510.80 unknown https://doi.org/10.1248/CPB.37.560
[15-(5,5-Dimethyl-6-methylideneoctan-2-yl)-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14312796 Click to see CCC(=C)C(C)(C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 510.80 unknown https://doi.org/10.1248/CPB.37.560
https://doi.org/10.1016/0031-9422(91)83212-4
[7,12,16-Trimethyl-15-(6-methylheptan-2-yl)-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14312805 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1OC(=O)C)C)C(C)CCCC(C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
Cycloartenol acetate 13023741 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.37.560
Cyclolaudenol acetate 6427354 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 482.80 unknown https://doi.org/10.1248/CPB.37.560
Cyclopenta[a]cyclopropa[e]phenanthren-7-one, perhydro-1-(1,5-dimethylhexyl)-3a,6,6,12a-tetramethyl 628597 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)83212-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(3S,5S,9S,10R,13S,14S)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-[(1S)-1-[(5R,6R)-5-methyl-6-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]ethyl]-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 118701246 Click to see CC1CCC(OC1OC2C(C(C(C(O2)C)O)O)O)C(C)C3CCC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C 887.10 unknown https://doi.org/10.1111/J.1467-3010.1976.TB00781.X
https://doi.org/10.1016/0040-4039(92)88086-K
https://doi.org/10.1016/0163-7258(80)90011-X
CID 147894 147894 Click to see CC1CCC(OC1OC2C(C(C(C(O2)C)O)O)O)C(C)C3CCC4C3(CCC5C4=CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C 885.00 unknown https://doi.org/10.1021/JO00107A018
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1248/CPB.37.560
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
Atpenin A5 54676868 Click to see CC(CC(C)C(=O)C1=C(C(=C(NC1=O)OC)OC)O)C(CCl)Cl 366.20 unknown https://doi.org/10.1016/S0031-9422(97)80008-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 138454316 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(00)98486-3
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(00)98486-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)98486-3
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(00)98486-3

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.