Hemidesmus indicus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Hemidesmus indicus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Internal ID UUID64404bda922e2107336062
Scientific name Hemidesmus indicus
Authority (L.) R.Br. ex Schult.
First published in Syst. Veg., ed. 15 bis [Roemer & Schultes] 6: 126. 1820 [Aug-Dec 1820] , isonym

Description Top

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Synonyms Top

Scientific name Authority First published in
Periploca malabarica Burm. ex Decne. Prodr. 8: 499 (1844)
Hemidesmus pubescens Wight & Arn. Contr. Bot. India : 63 (1834)
Periploca indica L. Sp. Pl. : 211 (1753)

Common names Top

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Language Common/alternative name
English indian sarsaparilla
Arabic عشبة النار الهندية
Bengali অনন্তমূল
dv ނަންނާރި
Hindi अनंतमूल
Kannada ಸೊಗದೆ ಬೇರು
Malayalam നറുനീണ്ടി
Oriya ଅନନ୍ତ
Punjabi ਅਨੰਤਮੂਲ
sa क्षीरिणीसस्यम्
Sinhala ඉරමුසු
Tamil நன்னாரி
Tamil கிருஸ்ணவல்லி
Tamil நறு நெட்டி
Telugu సుగంధిపాల
Urdu اننت مول

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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001104567
UNII G64J165NAI
Tropicos 2609794
KEW urn:lsid:ipni.org:names:60443873-2
The Plant List tro-2609794
Open Tree Of Life 65877
Observations.org 276176
NCBI Taxonomy 63476
IPNI 98256-1
iNaturalist 519938
GBIF 3576885
Freebase /m/0d9pbp
EOL 2900147
Elurikkus 644341
USDA GRIN 402594
Wikipedia Hemidesmus_indicus

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
2-Hydroxy-4-methoxybenzaldehyde, a more effective antifungal aroma than vanillin and its derivatives against Fusarium graminearum, destroys cell membranes, inhibits DON biosynthesis, and performs a promising antifungal effect on wheat grains Li Q, Wang C, Xiao H, Zhang Y, Xie Y Front Microbiol 26-Feb-2024
PMCID:PMC10925628
doi:10.3389/fmicb.2024.1359947
PMID:38468857
Eleven years of disease free survival in a case of Invasive Ductal Carcinoma (IDC) Rt Breast grade 3, stage 3, treated with add on Ayurveda treatment: A case report Nimbalkar R, Baheti AM, Pawar AT, Tagalpallewar AA, Nimbalkar MR J Ayurveda Integr Med 01-Feb-2024
PMCID:PMC10847158
doi:10.1016/j.jaim.2023.100881
PMID:38306823
Ayurvedic clinical decision-making methods to predict, prevent and manage childhood allergic disorders Karthik KP, Dileep A, Rajagopala S, Arun Kumar M, Dharmarajan P, Vellela J J Ayurveda Integr Med 18-Jan-2024
PMCID:PMC10828817
doi:10.1016/j.jaim.2023.100857
PMID:38237455
Optimization of ultrasound-aided extraction of bioactive ingredients from Vitis vinifera seeds using RSM and ANFIS modeling with machine learning algorithm Kunjiappan S, Ramasamy LK, Kannan S, Pavadai P, Theivendren P, Palanisamy P Sci Rep 12-Jan-2024
PMCID:PMC10786918
doi:10.1038/s41598-023-49839-y
PMID:38216594
Staphylococcus aureus biofilm: Formulation, regulatory, and emerging natural products-derived therapeutics Wu X, Wang H, Xiong J, Yang GX, Hu JF, Zhu Q, Chen Z Biofilm 01-Jan-2024
PMCID:PMC10827693
doi:10.1016/j.bioflm.2023.100175
PMID:38298832
Plant-Derived Epi-Nutraceuticals as Potential Broad-Spectrum Anti-Viral Agents Gabbianelli R, Shahar E, de Simone G, Rucci C, Bordoni L, Feliziani G, Zhao F, Ferrati M, Maggi F, Spinozzi E, Mahajna J Nutrients 08-Nov-2023
PMCID:PMC10675658
doi:10.3390/nu15224719
PMID:38004113
An in vivo and in silico evaluation of the hepatoprotective potential of Gynura procumbens: A promising agent for combating hepatotoxicity Tithi TI, Tahsin MR, Anjum J, Zaman TS, Aktar F, Bahar NB, Tasnim S, Sultana A, Jahan I, Afrin SS, Akter T, Sen P, Koly FJ, Reza MS, Chowdhury JA, Kabir S, Chowdhury AA, Amran MS PLoS One 15-Sep-2023
PMCID:PMC10503776
doi:10.1371/journal.pone.0291125
PMID:37713406
Stimulators of immunogenic cell death for cancer therapy: focusing on natural compounds Amiri M, Molavi O, Sabetkam S, Jafari S, Montazersaheb S Cancer Cell Int 13-Sep-2023
PMCID:PMC10500939
doi:10.1186/s12935-023-03058-7
PMID:37705051
Withania somnifera extracts induced attenuation of HIV-1: a mechanistic approach to restrict viral infection Jadaun P, Harshithkumar R, Gaikwad SY, Seniya C, Borse S, Gawai AA, Chavan-Gautam P, Tillu G, Mukherjee A Virol J 03-Aug-2023
PMCID:PMC10401819
doi:10.1186/s12985-023-02130-y
PMID:37537596
Uttarabasti in bladder neck contracture following transurethral resection of prostate: A case report Pokhrel SM, Sharma A, Singh M J Ayurveda Integr Med 25-Jul-2023
PMCID:PMC10388190
doi:10.1016/j.jaim.2023.100772
PMID:37499589
Biological Activity and Structural Diversity of Steroids Containing Aromatic Rings, Phosphate Groups, or Halogen Atoms Dembitsky VM Molecules 20-Jul-2023
PMCID:PMC10384810
doi:10.3390/molecules28145549
PMID:37513423
An In Silico Molecular Modelling-Based Prediction of Potential Keap1 Inhibitors from Hemidesmus indicus (L.) R.Br. against Oxidative-Stress-Induced Diseases Vellur S, Pavadai P, Babkiewicz E, Ram Kumar Pandian S, Maszczyk P, Kunjiappan S Molecules 03-Jun-2023
PMCID:PMC10254626
doi:10.3390/molecules28114541
PMID:37299017
Efficacy of Jatyadi, Madhughrita and honey tulle in wound management: a three-arm randomized controlled clinical trial Prasannan D, Shindhe PS, Jadar PG, Killedar RS, Priyanka K. J Ayurveda Integr Med 02-Jun-2023
PMCID:PMC10242641
doi:10.1016/j.jaim.2023.100719
PMID:37271064
A Bioactive Compound-Loaded Zinc-Aminoclay Encapsulated, Pickering Emulsion System for Treating Acne-Inducing Microbes Kim SH, Bae IS, Lee HU, Moon JY, Lee YC Int J Mol Sci 02-Jun-2023
PMCID:PMC10253637
doi:10.3390/ijms24119669
PMID:37298619
HPTLC and GC–MS finger-printing of two potential multifunctional siddha tailams: Mathan and maha megarajanga tailam Senthilnathan S, Jayaraman S, Priya Veeraraghavan V, Masood Khan J, Ahmed MZ, Ahmad A, Gnanamani A Saudi J Biol Sci 01-Jun-2023
PMCID:PMC10276281
doi:10.1016/j.sjbs.2023.103700
PMID:37333677

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 / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxysalicylic acid 75231 Click to see COC1=CC(=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/0041-0101(94)90314-X
https://doi.org/10.1016/S0041-0101(98)00076-2
> Benzenoids / Phenols / Benzenediols / Catechols
Epinephrine 5816 Click to see CNCC(C1=CC(=C(C=C1)O)O)O 183.20 unknown https://doi.org/10.1016/S0031-9422(96)00393-7
> Benzenoids / Phenols / Methoxyphenols
2-Hydroxy-4-methoxybenzaldehyde 69600 Click to see COC1=CC(=C(C=C1)C=O)O 152.15 unknown https://doi.org/10.1016/S0031-9422(00)97582-4
Isovanillin 12127 Click to see COC1=C(C=C(C=C1)C=O)O 152.15 unknown https://doi.org/10.1016/S0031-9422(00)97582-4
> Lignans, neolignans and related compounds / Coumarinolignans
2-(3-Hydroxy-5-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 15931469 Click to see COC1=CC(=CC(=C1)O)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO 386.40 unknown https://doi.org/10.1002/CHIN.199237311
5-Hydroxy-3-(hydroxymethyl)-2-(3,4,5-trimethoxyphenyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 15931468 Click to see COC1=CC(=CC(=C1OC)OC)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)O)CO 416.40 unknown https://doi.org/10.1002/CHIN.199237311
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/S0031-9422(00)97582-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupanone 129730785 Click to see CC(C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(=O)CCC5(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97582-4
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)97582-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3S,4R,6R)-6-[[(3S,8R,9S,10R,13R,14S,17S)-14-hydroxy-17-[(1S)-1-hydroxyethyl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-2-methyloxane-3,4-diol 101594607 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CC=C3C2)O)C(C)O)C)C)O)O 464.60 unknown https://doi.org/10.1016/0031-9422(91)84141-E
(2R,3S,4S,6R)-6-[[(3S,8R,9S,10R,13R,14S,17S)-14-hydroxy-17-[(1S)-1-hydroxyethyl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-3-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-2-methyloxan-4-ol 102014181 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3CCC4(C5CCC6(C(CCC6(C5CC=C4C3)O)C(C)O)C)C)C)OC)O 608.80 unknown https://doi.org/10.1016/S0031-9422(99)00611-1
https://doi.org/10.1016/0031-9422(85)80047-9
(2R,3S,4S,6S)-6-[(2R,3S,4S,6S)-4-hydroxy-6-[(2R,3S,4S,6R)-4-hydroxy-6-[[(3S,8R,9S,10R,13R,14S,17S)-14-hydroxy-17-[(1S)-1-hydroxyethyl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-2-methyloxan-3-yl]oxy-2-methyloxan-3-yl]oxy-2-methyloxane-3,4-diol 101664026 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C6CCC7(C(CCC7(C6CC=C5C4)O)C(C)O)C)C)C)C)O)O 724.90 unknown https://doi.org/10.1016/S0031-9422(00)86891-0
(2S,3R,4S,5R)-2-[(2R,3S,4S,6S)-6-[(3R,4R,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,6R)-4-hydroxy-6-[[(3S,8R,9S,10R,13R,14S,17S)-14-hydroxy-17-[(1S)-1-hydroxyethyl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-2-methyloxan-3-yl]oxyoxan-3-yl]oxy-4-hydroxy-2-methyloxan-3-yl]oxyoxane-3,4,5-triol 102446079 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CC=C3C2)O)C(C)O)C)C)O)OC6C(C(C(CO6)OC7CC(C(C(O7)C)OC8C(C(C(CO8)O)O)O)O)O)O 859.00 unknown https://doi.org/10.1016/S0031-9422(96)00393-7
(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,6R)-6-[[(3S,8R,10R,13R,14S,17S)-14-hydroxy-17-[(1S)-1-hydroxyethyl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-6-methyloxane-3,5-diol 163186609 Click to see CC1C(C(C(C(O1)OC2C(OC(CC2OC)OC3CCC4(C5CCC6(C(CCC6(C5CC=C4C3)O)C(C)O)C)C)C)O)OC)O 638.80 unknown https://doi.org/10.1016/S0031-9422(99)00611-1
(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,6R)-6-[[(3S,8R,9S,10R,13R,14S,17S)-14-hydroxy-17-[(1S)-1-hydroxyethyl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-6-methyloxane-3,5-diol 102014180 Click to see CC1C(C(C(C(O1)OC2C(OC(CC2OC)OC3CCC4(C5CCC6(C(CCC6(C5CC=C4C3)O)C(C)O)C)C)C)O)OC)O 638.80 unknown https://doi.org/10.1016/0031-9422(85)80047-9
https://doi.org/10.1016/S0031-9422(99)00611-1
(3S,8S,9R,10R,12R,13R,14R,17S)-17-[(1S)-1-hydroxyethyl]-3-[(2R,4R,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-6-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthrene-8,12,14,17-tetrol 102446077 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3CCC4(C5CC(C6(C(CCC6(C5(CC=C4C3)O)O)(C(C)O)O)C)O)C)C)O)OC7C(C(C(C(O7)CO)O)O)O 818.90 unknown https://doi.org/10.1016/S0031-9422(96)00393-7
[(1S)-1-[(3S,8R,9S,10R,13R,14S,17S)-3-[(2R,4R,5R,6R)-5-[(2S,4S,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]ethyl] acetate 101664025 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3CCC4(C5CCC6(C(CCC6(C5CC=C4C3)O)C(C)OC(=O)C)C)C)C)O)O 650.80 unknown https://doi.org/10.1016/S0031-9422(00)86891-0
6-[[14-Hydroxy-17-(1-hydroxyethyl)-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-3-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-2-methyloxan-4-ol 162979292 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3CCC4(C5CCC6(C(CCC6(C5CC=C4C3)O)C(C)O)C)C)C)OC)O 608.80 unknown https://doi.org/10.1016/S0031-9422(99)00611-1
https://doi.org/10.1016/0031-9422(85)80047-9
> 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)97582-4
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)97582-4
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Penicipyran D 139590417 Click to see CC1=C(C=C2C=C(OC(=O)C2=C1O)CC(CC(C)O)O)O 294.30 unknown https://doi.org/10.1016/0031-9422(85)80047-9
https://doi.org/10.1016/S0031-9422(99)00611-1

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