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Piper hostmannianum

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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 UUID644001ce0dedd993562886
Scientific name Piper hostmannianum
Authority C.DC.
First published in Prodr. 16(1): 287 (1869)

Description Top

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Synonyms Top

Scientific name Authority First published in
Piper paracaimanum C.DC. Notizbl. Königl. Bot. Gart. Berlin 6: 490 (1917)
Piper puberulibaccum C.DC. Notizbl. Königl. Bot. Gart. Berlin 6: 487 (1917)
Piper subcrassifolium Yunck. Bol. Soc. Venez. Ci. Nat. 23: 68 (1962)
Piper nemorale C.DC. Verh. Bot. Vereins Prov. Brandenburg 47: 109 (1905)
Piper hostmannianum var. glabrirameum Trel. & Yunck. Piperac. N. South Amer. : 307 (1950)
Artanthe hostmanniana Miq. London J. Bot. 4: 465 (1845)
Artanthe ramiflora Miq. ex C.DC. Prodr. [A. P. de Candolle] 16(1): 288. 1869 [mid Nov 1869]
Piper hostmannianum var. ramiflorum C.DC. Prodr. 16(1): 287–288 1869
Artanthe berbicense Miq. Syst. Piperac. 500
Piper gleasonii var. wonotoboense Yunck. Piperac. N. South Amer. : 364 (1950)

Common names Top

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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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000478999
Tropicos 25000641
INPN 734589
KEW urn:lsid:ipni.org:names:681692-1
The Plant List kew-2558138
Open Tree Of Life 232999
NCBI Taxonomy 511544
IUCN Red List 179304275
IPNI 681692-1
GBIF 7305149
CMAUP NPO14386

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
Applications of Friedel–Crafts reactions in total synthesis of natural products Heravi MM, Zadsirjan V, Saedi P, Momeni T RSC Adv 03-Dec-2018
PMCID:PMC9091380
doi:10.1039/c8ra07325b
PMID:35558228
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773
OVICIDAL EFFECT OF PIPERACEAE SPECIES ON Biomphalaria glabrata, Schistosoma mansoni HOST Rapado LN, Lopes PO, Yamaguchi LF, Nakano E Rev Inst Med Trop Sao Paulo 01-Nov-2013
PMCID:PMC4105091
doi:10.1590/S0036-46652013000600009
PMID:24213196
Dihydrochalcones and benzoic acid derivatives from Piper dennisii. Cabanillas BJ, Le Lamer AC, Castillo D, Arevalo J, Estevez Y, Rojas R, Valadeau C, Bourdy G, Sauvain M, Fabre N Planta Med 01-Jun-2012
doi:10.1055/S-0031-1298459
PMID:22516933
Antimicrobial Activity of Piper gaudichaudianum Kuntze and Its Synergism with Different Antibiotics Puhl MC, Cortez DA, Ueda-Nakamura T, Nakamura CV, Filho BP Molecules 01-Dec-2011
PMCID:PMC6264199
doi:10.3390/molecules16129925
PMID:22134399
Antimalarial activity of a cis-terpenone Mayer DG, Bruce M, Kochurova O, Stewart JK, Zhou Q Malar J 25-Jun-2009
PMCID:PMC2711970
doi:10.1186/1475-2875-8-139
PMID:19555505
Activity-guided isolation of antiplasmodial dihydrochalcones and flavanones from Piper hostmannianum var. berbicense. Portet B, Fabre N, Roumy V, Gornitzka H, Bourdy G, Chevalley S, Sauvain M, Valentin A, Moulis C Phytochemistry 01-May-2007
doi:10.1016/J.PHYTOCHEM.2007.02.006
PMID:17397884
Benzoic acid derivatives from Piper species and their fungitoxic activity against Cladosporium cladosporioides and C. sphaerospermum. Lago JH, Ramos CS, Casanova DC, Morandim Ade A, Bergamo DC, Cavalheiro AJ, Bolzani Vda S, Furlan M, Guimarães EF, Young MC, Kato MJ J Nat Prod 01-Nov-2004
doi:10.1021/NP030530J
PMID:15568762
A chromene an isoprenylated methyl hydroxybenzoate and a C-methyl flavanone from the bark of Piper hostmannianum Pedro P., D. Díaz, Tiberio Arias C., Pedro Joseph-Nathan Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84792-5

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 / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methyl 3-(2,3-dihydroxy-3-methylbutyl)-4-hydroxybenzoate 11184361 Click to see CC(C)(C(CC1=C(C=CC(=C1)C(=O)OC)O)O)O 254.28 unknown https://doi.org/10.1021/NP030530J
methyl 3-[(2S)-2,3-dihydroxy-3-methylbutyl]-4-hydroxybenzoate 163006673 Click to see CC(C)(C(CC1=C(C=CC(=C1)C(=O)OC)O)O)O 254.28 unknown https://doi.org/10.1021/NP030530J
Methyl 4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)benzoate 13846908 Click to see CC(=C)C(CC1=C(C=CC(=C1)C(=O)OC)O)O 236.26 unknown https://doi.org/10.1021/NP030530J
Methyl 4-hydroxy-3-(3'-methyl-2'-butenyl)benzoate 127925 Click to see CC(=CCC1=C(C=CC(=C1)C(=O)OC)O)C 220.26 unknown https://doi.org/10.1021/NP030530J
methyl 4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]benzoate 92466200 Click to see CC(=C)C(CC1=C(C=CC(=C1)C(=O)OC)O)O 236.26 unknown https://doi.org/10.1021/NP030530J
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z,9R)-9-hydroxyoctadec-12-enoic acid 5312848 Click to see CCCCCC=CCCC(CCCCCCCC(=O)O)O 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)84792-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
11alpha-Hydroxyandrosta-1,4-diene-3,17-dione 111337 Click to see CC12CC(C3C(C1CCC2=O)CCC4=CC(=O)C=CC34C)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
(3S,8S,9S,10R,13S,14S,17S)-10,13-dimethyl-17-[(1S)-1-(methylamino)ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine 102090481 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)C)NC 330.50 unknown via CMAUP database
Kurchessine 442979 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)C)N(C)C 372.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methylenecholesterol 92113 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 18-hydroxysteroids
[(3S,8R,9S,10R,13R,14S,17S)-3-(dimethylamino)-17-[(1S)-1-(dimethylamino)ethyl]-10-methyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-13-yl]methanol 14543701 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)CO)N(C)C 388.60 unknown via CMAUP database
Holadysenterine 16742955 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)CO)N(C(=O)C)O 390.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Hydrocortisone 5754 Click to see CC12CCC(=O)C=C1CCC3C2C(CC4(C3CCC4(C(=O)CO)O)C)O 362.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,13-dimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one 21573748 Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)CN1 327.50 unknown via CMAUP database
Holanamine 76308534 Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)C=N1 325.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
Holadysine 102093813 Click to see CCC1C(=O)CC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C 329.50 unknown via CMAUP database
Holarrhimine 15559632 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)CO)N 332.50 unknown via CMAUP database
Irehdiamine B 15560372 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C)N 330.50 unknown via CMAUP database
Pregn-5-en-18-ol, 20-amino-3-(methylamino)-, (3beta,20S)- 22214001 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)CO)N 346.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
(1R,2S,5S,6S,9R,12S,13R,16S,20S)-16-(dimethylamino)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-20-ol 102093825 Click to see CC1C2CCC3C2(CCC4C3C(C=C5C4(CCC(C5)N(C)C)C)O)CN1C 372.60 unknown via CMAUP database
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one 21573749 Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)CN1C 341.50 unknown via CMAUP database
(1S,2S,5S,6S,9R,12S,13R,16S,17R,18R,20R)-16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosane-18,20-diol 101529338 Click to see CC1C(CCC2(C1(CC(C3C2CCC45C3CCC4C(N(C5)C)C)O)O)C)N(C)C 404.60 unknown via CMAUP database
Con-5-enin-12-ol, 3-(dimethylamino)-, 4-methyl-3-pentenoate (ester), (3beta,12beta)- 11225162 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)OC(=O)CC=C(C)C 468.70 unknown via CMAUP database
Conessine 441082 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C 356.60 unknown via CMAUP database
Holadienine 12310532 Click to see CC1C2CCC3C2(CCC4C3CCC5=CC(=O)C=CC45C)CN1C 325.50 unknown via CMAUP database
Holarrhenine 12310556 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)O 372.60 unknown via CMAUP database
Isoconessimine 11772257 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1C 342.60 unknown via CMAUP database
Kurcholessine 20054951 Click to see CC1C(CCC2(C1(CC(C3C2CCC45C3CCC4C(N(C5)C)C)O)O)C)N(C)C 404.60 unknown via CMAUP database
N,N-Dimethylconanin-5-en-3alpha-amine 12303833 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C 356.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84792-5
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/10.1016/S0031-9422(00)84792-5
24-ethylcholesta-5,23E-dien-3beta-ol 5283668 Click to see CCC(=CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
(1R,2S,5S,6S,9R,12S,13R,16S)-6,13-dimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine 12303820 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N)C)CN1 314.50 unknown via CMAUP database
(1R,2S,5S,6S,9R,12S,13R,16S)-7-hydroxy-N,N,6,13-tetramethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine 101529337 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1O 358.60 unknown via CMAUP database
Conessimine 12303831 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1 342.60 unknown via CMAUP database
Conimin 101686 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1 328.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Methyl 2,2-dimethylchromene-6-carboxylate 5316881 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C(=O)OC)C 218.25 unknown https://doi.org/10.1021/NP030530J
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Paravallarine 442980 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)C(=O)O1 343.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolines
Conckurchine 76330309 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N)C)C=N1 312.50 unknown via CMAUP database
Conessidine 22214027 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)C=N1 326.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
methyl 2,4-dihydroxy-6-methoxy-3-methyl-5-[(1R,6R)-4-(4-methylpent-3-enyl)-6-phenylcyclohex-3-ene-1-carbonyl]benzoate 16681189 Click to see CC1=C(C(=C(C(=C1O)C(=O)OC)OC)C(=O)C2CC=C(CC2C3=CC=CC=C3)CCC=C(C)C)O 478.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
Methyl 2,4-dihydroxy-6-methoxy-3-methyl-5-[4-(4-methylpent-3-enyl)-6-phenylcyclohex-3-ene-1-carbonyl]benzoate 73307028 Click to see CC1=C(C(=C(C(=C1O)C(=O)OC)OC)C(=O)C2CC=C(CC2C3=CC=CC=C3)CCC=C(C)C)O 478.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R)-5,7-dihydroxy-6-[(1R,6R)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]-2-phenyl-2,3-dihydrochromen-4-one 162933592 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C3=C(C=C2O)OC(CC3=O)C4=CC=CC=C4)O 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
(2S)-5,7-dihydroxy-6-[(1R,6R)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]-2-phenyl-2,3-dihydrochromen-4-one 14781323 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C3=C(C=C2O)OC(CC3=O)C4=CC=CC=C4)O 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
Linderatone 14781322 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C3=C(C=C2O)OC(CC3=O)C4=CC=CC=C4)O 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-6-methyl-2-phenyl-4-benzopyrone 114429 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/S0031-9422(00)84792-5
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-(3,6-dihydroxy-1-methoxy-6-methyl-9-propan-2-yl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-4-yl)-3-phenylpropan-1-one 73307027 Click to see CC(C)C1CCC(C2C1C3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)(C)O 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
1-(5-Hydroxy-3-methoxy-9-methyl-12-propan-2-yl-8-oxatricyclo[7.3.1.02,7]trideca-2,4,6-trien-6-yl)-3-phenylpropan-1-one 73307029 Click to see CC(C)C1CCC2(CC1C3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
1-[(1R,9R,12S)-5-hydroxy-3-methoxy-9-methyl-12-propan-2-yl-8-oxatricyclo[7.3.1.02,7]trideca-2,4,6-trien-6-yl]-3-phenylpropan-1-one 163022421 Click to see CC(C)C1CCC2(CC1C3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)C 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
1-[(5aR,6S,9S,9aS)-3,6-dihydroxy-1-methoxy-6-methyl-9-propan-2-yl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-4-yl]-3-phenylpropan-1-one 16681188 Click to see CC(C)C1CCC(C2C1C3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)(C)O 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
1-[2,6-Dihydroxy-4-methoxy-3-(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)phenyl]-3-phenylpropan-1-one 14237695 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C=C(C(=C2O)C(=O)CCC3=CC=CC=C3)O)OC 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
2',6'-Dihydroxy-4'-methoxydihydrochalcone 169676 Click to see COC1=CC(=C(C(=C1)O)C(=O)CCC2=CC=CC=C2)O 272.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
https://doi.org/10.1055/S-0031-1298459
Adunctin E 42607690 Click to see CC(C)C1CCC(C2C1C3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)(C)O 424.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006
Methyllinderatin 42607684 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C=C(C(=C2O)C(=O)CCC3=CC=CC=C3)O)OC 408.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.02.006

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