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Asparagus adscendens

Asparagus adscendens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644014a0a12b0776758782
Scientific name Asparagus adscendens
Authority Roxb.
First published in Fl. Ind. ed. 1832 , 2: 153 (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Asparagopsis adscendens Kunth Enum. Pl. 5: 102 (1850)
Asparagus satawur J.A.Murr. Drugs Pl. Sind : 24 (1881)
Protasparagus adscendens (Roxb.) Kamble J. Econ. Taxon. Bot. 15: 707 (1991 publ. 1992)

Common names Top

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Language Common/alternative name
Bengali শতমূলী
Chinese 升天冬
Chinese 昇天冬

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
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Pakistan
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000631214
UNII LLI0845BR7
Tropicos 18407014
KEW urn:lsid:ipni.org:names:530993-1
The Plant List kew-274923
Open Tree Of Life 494665
NCBI Taxonomy 722773
IPNI 530993-1
iNaturalist 862178
GBIF 2768799
EOL 987591
USDA GRIN 407189
PFAF Asparagus adscendens

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
Vegetation–edaphic correlation and importance value index in himalayan ‘ecotone’ temperate conifer forest using the multivariate technique Ali F, Zeb M, Amin M, Rajpar MN, Hidayat S, Khan WR Saudi J Biol Sci 24-Mar-2024
PMCID:PMC11000104
doi:10.1016/j.sjbs.2024.103983
PMID:38590389
Potential Immunoregulatory Mechanism of Plant Saponins: A Review Shen L, Luo H, Fan L, Tian X, Tang A, Wu X, Dong K, Su Z Molecules 23-Dec-2023
PMCID:PMC10780299
doi:10.3390/molecules29010113
PMID:38202696
Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU Can J Infect Dis Med Microbiol 28-Oct-2023
PMCID:PMC10625492
doi:10.1155/2023/1860084
PMID:37927532
A combined approach of DNA metabarcoding collectively enhances the detection efficiency of medicinal plants in single and polyherbal formulations Travadi T, Shah AP, Pandit R, Sharma S, Joshi C, Joshi M Front Plant Sci 15-May-2023
PMCID:PMC10225634
doi:10.3389/fpls.2023.1169984
PMID:37255553
Shatavarin-IV saponin adjuvant elicits IgG and IgG2b responses against Staphylococcus aureus bacterin in a murine model Palanisamy A, Sharma R, Singh PP, Sharma U, Patil RD, Mal G, Singh B Heliyon 11-Apr-2023
PMCID:PMC10133762
doi:10.1016/j.heliyon.2023.e15339
PMID:37123899
Adaptogenic property of Asparagus racemosus: Future trends and prospects Singh N, Garg M, Prajapati P, Singh PK, Chopra R, Kumari A, Mittal A Heliyon 01-Apr-2023
PMCID:PMC10121633
doi:10.1016/j.heliyon.2023.e14932
PMID:37095959
Biogenic Synthesis of Copper-Based Nanomaterials Using Plant Extracts and Their Applications: Current and Future Directions Vincent J, Lau KS, Evyan YC, Chin SX, Sillanpää M, Chia CH Nanomaterials (Basel) 23-Sep-2022
PMCID:PMC9565561
doi:10.3390/nano12193312
PMID:36234439
Neuropharmacological Effects of Terpenoids on Preclinical Animal Models of Psychiatric Disorders: A Review Mony TJ, Elahi F, Choi JW, Park SJ Antioxidants (Basel) 18-Sep-2022
PMCID:PMC9495487
doi:10.3390/antiox11091834
PMID:36139909
Phytochemical Classification of Medicinal Plants Used in the Treatment of Kidney Disease Based on Traditional Persian Medicine Rabizadeh F, Mirian MS, Doosti R, Kiani-Anbouhi R, Eftekhari E Evid Based Complement Alternat Med 31-Jul-2022
PMCID:PMC9357710
doi:10.1155/2022/8022599
PMID:35958915
A Critical Review of the Antimicrobial and Antibiofilm Activities of Green-Synthesized Plant-Based Metallic Nanoparticles Luzala MM, Muanga CK, Kyana J, Safari JB, Zola EN, Mbusa GV, Nuapia YB, Liesse JM, Nkanga CI, Krause RW, Balčiūnaitienė A, Memvanga PB Nanomaterials (Basel) 27-May-2022
PMCID:PMC9182092
doi:10.3390/nano12111841
PMID:35683697
Chemistry, Biosynthesis and Pharmacology of Sarsasapogenin: A Potential Natural Steroid Molecule for New Drug Design, Development and Therapy Mustafa NH, Sekar M, Fuloria S, Begum MY, Gan SH, Rani NN, Ravi S, Chidambaram K, Subramaniyan V, Sathasivam KV, Jeyabalan S, Uthirapathy S, Ponnusankar S, Lum PT, Bhalla V, Fuloria NK Molecules 21-Mar-2022
PMCID:PMC8955086
doi:10.3390/molecules27062032
PMID:35335393
Green Synthesis and Characterization of Copper Nanoparticles Using Fortunella margarita Leaves Amjad R, Mubeen B, Ali SS, Imam SS, Alshehri S, Ghoneim MM, Alzarea SI, Rasool R, Ullah I, Nadeem MS, Kazmi I Polymers (Basel) 13-Dec-2021
PMCID:PMC8705435
doi:10.3390/polym13244364
PMID:34960915
Occurrence and Health Risk Assessment of Aflatoxins through Intake of Eastern Herbal Medicines Collected from Four Districts of Southern Punjab—Pakistan Javed A, Naeem I, Benkerroum N, Riaz M, Akhtar S, Ismail A, Sajid M, Tayyab Khan M, Ismail Z Int J Environ Res Public Health 10-Sep-2021
PMCID:PMC8466447
doi:10.3390/ijerph18189531
PMID:34574455
Mixed phytochemicals mediated synthesis of copper nanoparticles for anticancer and larvicidal applications Rajagopal G, Nivetha A, Sundar M, Panneerselvam T, Murugesan S, Parasuraman P, Kumar S, Ilango S, Kunjiappan S Heliyon 22-Jun-2021
PMCID:PMC8246643
doi:10.1016/j.heliyon.2021.e07360
PMID:34235284
Status and consolidated list of threatened medicinal plants of India Gowthami R, Sharma N, Pandey R, Agrawal A Genet Resour Crop Evol 25-May-2021
PMCID:PMC8148398
doi:10.1007/s10722-021-01199-0
PMID:34054223

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown https://doi.org/10.1016/0031-9422(82)83046-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown https://doi.org/10.1016/0031-9422(82)83046-X
Methyl pentacosanoate 41431 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC 396.70 unknown https://doi.org/10.1016/0031-9422(82)83046-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Tetracosyl tetracosanoate 3083668 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCCCCCCCC 705.30 unknown https://doi.org/10.1016/0031-9422(82)83046-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Hexadec-8-enoic acid 119631 Click to see CCCCCCCC=CCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1016/0031-9422(82)83046-X
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/0031-9422(82)83046-X
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1016/0031-9422(82)83046-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1016/S0031-9422(82)85045-0
Spirost-5-en-3-ol 234096 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1016/S0031-9422(82)85045-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 162930704 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)C)O)O)O)O)O)C)C)C)OC1 869.00 unknown https://doi.org/10.1016/S0031-9422(00)80399-4
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 162928668 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)C)O)O)O)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown https://doi.org/10.1016/S0031-9422(00)80399-4
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 162884199 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)C)O)O)O)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1063.20 unknown https://doi.org/10.1016/S0031-9422(00)80399-4
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol 162954339 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)C)O)O)O)O)O)O)C)C)C)OC1 722.90 unknown https://doi.org/10.1016/S0031-9422(00)80399-4
2-[[4,5-Dihydroxy-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 162930703 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)C)O)O)O)O)O)C)C)C)OC1 869.00 unknown https://doi.org/10.1016/S0031-9422(00)80399-4
2-[[4,5-Dihydroxy-6-[[6-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 162928667 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)C)O)O)O)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown https://doi.org/10.1016/S0031-9422(00)80399-4
2-[[4,5-Dihydroxy-6-[[6-methoxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 162884198 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)C)O)O)O)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1063.20 unknown https://doi.org/10.1016/S0031-9422(00)80399-4
2-[4-Hydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 158680 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1 887.10 unknown https://doi.org/10.1016/0031-9422(82)83046-X
2-Methyl-6-[[3,4,5-trihydroxy-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxyoxan-2-yl]methoxy]oxane-3,4,5-triol 75026393 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)C)O)O)O)O)O)O)C)C)C)OC1 722.90 unknown https://doi.org/10.1016/S0031-9422(00)80399-4
Asparanin A 21575007 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 unknown https://doi.org/10.1016/0031-9422(82)83046-X
Asparanin B 441896 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1 887.10 unknown https://doi.org/10.1016/0031-9422(82)83046-X
Schidigerasaponin D5 3272925 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)OC1 740.90 unknown https://doi.org/10.1016/0031-9422(82)83046-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-dihydroxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 102061530 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(CO5)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)C(C)C 706.90 unknown https://doi.org/10.1016/0031-9422(90)87114-A
[(2S,3R,4S,5R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-dihydroxyoxan-3-yl] tetracosanoate 102061529 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OC1C(C(COC1OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)C=CC(CC)C(C)C)C)C)O)O 895.40 unknown https://doi.org/10.1016/0031-9422(90)87114-A
[2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-dihydroxyoxan-3-yl] tetracosanoate 163045666 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OC1C(C(COC1OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)C=CC(CC)C(C)C)C)C)O)O 895.40 unknown https://doi.org/10.1016/0031-9422(90)87114-A
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(82)85045-0
2-[2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-dihydroxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 78134680 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(CO5)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)C(C)C 706.90 unknown https://doi.org/10.1016/0031-9422(90)87114-A
Beta-Sitosterol 222284 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(82)85045-0
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(82)83046-X
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(82)83046-X

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