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Crossosoma bigelovii

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401413f2dae250928662
Scientific name Crossosoma bigelovii
Authority S.Watson
First published in Proc. Amer. Acad. Arts 11: 122 (1876)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English ragged rockflower
Arabic متصالبة بيغلوفية

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Crossosoma bigelovii var. glaucum (Small) Kearney & Peebles Fl. Pl. Ferns Ariz. : 388 (1942)
Crossosoma bigelovii var. bigelovii

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
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Northwest
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000626483
USDA Plants CRBI2
Tropicos 9000002
KEW urn:lsid:ipni.org:names:316540-1
The Plant List kew-2743154
Open Tree Of Life 207317
NCBI Taxonomy 105808
Nature Serve 2.134829
IPNI 316540-1
iNaturalist 76482
GBIF 5362091
Freebase /m/05zx3h4
EOL 585111
Calflora (Californian flora) 2432
Wikipedia Crossosoma_bigelovii
CMAUP NPO27978

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
Phenolic Phytochemicals for Prevention and Treatment of Colorectal Cancer: A Critical Evaluation of In Vivo Studies De S, Paul S, Manna A, Majumder C, Pal K, Casarcia N, Mondal A, Banerjee S, Nelson VK, Ghosh S, Hazra J, Bhattacharjee A, Mandal SC, Pal M, Bishayee A Cancers (Basel) 03-Feb-2023
PMCID:PMC9913554
doi:10.3390/cancers15030993
PMID:36765950
Dalmanol biosyntheses require coupling of two separate polyketide gene clusters Zhou ZZ, Zhu HJ, Lin LP, Zhang X, Ge HM, Jiao RH, Tan RX Chem Sci 27-Nov-2018
PMCID:PMC6335865
doi:10.1039/c8sc03697g
PMID:30746075
Between semelparity and iteroparity: Empirical evidence for a continuum of modes of parity Hughes PW Ecol Evol 07-Sep-2017
PMCID:PMC5648687
doi:10.1002/ece3.3341
PMID:29075446
Concise Synthesis of 5-Methoxy-6-hydroxy-2-methylchromone-7-O- and 5-Hydroxy-2-methylchromone-7-O-rutinosides, Investigation of their Cytotoxic Activities against Several Human Tumor Cell Lines Wu B, Zhang W, Li Z, Gu L, Wang X, Wang PG J Org Chem 02-Mar-2011
PMCID:PMC3441829
doi:10.1021/jo102325s
PMID:21366286
High Throughput Extraction of Plant, Marine and Fungal Specimens for Preservation of Biologically Active Molecules McCloud TG Molecules 24-Jun-2010
PMCID:PMC6257593
doi:10.3390/molecules15074526
PMID:20657375
Development of HIF-1 inhibitors for cancer therapy Onnis B, Rapisarda A, Melillo G J Cell Mol Med 08-Aug-2009
PMCID:PMC2832082
doi:10.1111/j.1582-4934.2009.00876.x
PMID:19674190
Cytotoxic and HIF-1alpha inhibitory compounds from Crossosoma bigelovii. Klausmeyer P, Zhou Q, Scudiero DA, Uranchimeg B, Melillo G, Cardellina JH, Shoemaker RH, Chang CJ, McCloud TG J Nat Prod 22-May-2009
doi:10.1021/NP8006342
PMID:19405508

Phytochemical Profile Top

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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
> Alkaloids and derivatives / Yohimbine alkaloids
Ajmalicine 441975 Click to see 352.40 unknown https://doi.org/10.1021/NP8006342
Lamuran 251561 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1021/NP8006342
methyl (1R,15R,16S,20R)-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,18-pentaene-19-carboxylate 7067845 Click to see 352.40 unknown https://doi.org/10.1021/NP8006342
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
2,3-Bis((4-hydroxy-3-methoxyphenyl)methyl)butane-1,4-diol 586372 Click to see 362.40 unknown https://doi.org/10.1021/NP8006342
Secoisolariciresinol 65373 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 362.40 unknown https://doi.org/10.1021/NP8006342
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Matairesinol 119205 Click to see 358.40 unknown https://doi.org/10.1021/NP8006342
3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 345761 Click to see 358.40 unknown https://doi.org/10.1021/NP8006342
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
Strophanthidin 6185 Click to see 404.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(3S,5S,8R,9S,10S,13R,14S,17R)-5,14-dihydroxy-3-[(2S,3R,4R,6R)-3-methoxy-6-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 44139361 Click to see 710.80 unknown https://doi.org/10.1021/NP8006342
5,14-dihydroxy-3-[3-methoxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 56656798 Click to see CC1CC(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)OC)OC7C(C(C(C(O7)CO)O)O)O 710.80 unknown https://doi.org/10.1021/NP8006342
Convallatoxin 441852 Click to see 550.60 unknown via CMAUP database
k-Strophanthoside 20055295 Click to see 872.90 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
5-Hydroxy-6-methoxy-2-methyl-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 56657654 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C)O)OC)O)O)O)O)O)O 530.50 unknown https://doi.org/10.1021/NP8006342
5-Hydroxy-6-Methoxy-2-Methylchromone-7-O-Rutinoside 44139362 Click to see 530.50 unknown https://doi.org/10.1021/NP8006342
5,6-dihydroxy-2-methyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 44139363 Click to see 516.40 unknown https://doi.org/10.1021/NP8006342
5,6-Dihydroxy-2-methyl-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 56663796 Click to see 516.40 unknown https://doi.org/10.1021/NP8006342
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Eugenin 10189 Click to see 206.19 unknown https://doi.org/10.1021/NP8006342
Noreugenin 5375252 Click to see 192.17 unknown https://doi.org/10.1021/NP8006342
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5R)-5-[(E)-tetradec-5-enyl]oxolan-2-one 102157588 Click to see 280.40 unknown https://doi.org/10.1021/NP8006342
(5R)-5-tetradec-5-enyloxolan-2-one 162974355 Click to see 280.40 unknown https://doi.org/10.1021/NP8006342
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidine carboxylic acids and derivatives / Pyrrolidine carboxylic acids
(3R,4S)-4-hydroxy-1,1-dimethylpyrrolidin-1-ium-3-carboxylic acid 1801303 Click to see 160.19 unknown via CMAUP database

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