Typhonium flagelliforme - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

Internal ID UUID643feff9b0dbb084889401
Scientific name Typhonium flagelliforme
Authority (Roxb. ex Lodd., G.Lodd. & W.Lodd.) Blume
First published in Rumphia 1: 134 (1837)

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
Arum angulatum Griff. Not. Pl. Asiat. 3: 143 (1851)
Arum cuspidatum Blume Catalogus : 101 (1823)
Arum divaricatum L. Sp. Pl. : 966 (1753)
Arum flagelliferum Griff. Not. Pl. Asiat. 3: 144 (1851)
Arum flagelliforme Roxb. ex Lodd., G.Lodd. & W.Lodd. Bot. Cab. 4: t. 396 (1820)
Arum ptychiurum Zipp. ex Kunth Enum. Pl. 3: 26 (1841)
Typhonium cuspidatum Decne. Nouv. Ann. Mus. Hist. Nat. 3: 367 (1834)
Typhonium cuspidatum var. ptychiurum Blume Rumphia 1: 134. 1837
Typhonium flagelliferum Griff. Not. Pl. Asiat. 3: 144 (1851)
Typhonium flagelliforme var. angustissimum Ridl. J. Straits Branch Roy. Asiat. Soc. 59: 218. 1911
Typhonium hastiferum Miq. Fl. Ned. Ind. 3: 194 (1856)
Typhonium incurvatum Blatt. & McCann J. Bombay Nat. Hist. Soc. 35: 22 (1931)
Typhonium reinwardtianum de Vriese & Miq. Fl. Ned. Ind. 3: 195. 1856 (1856)
Typhonium sylvaticum Voigt Hort. Suburb. Calcutt. : 686 (1845)
Heterostalis flagelliformis Schott Oesterr. Bot. Wochenbl. 7: 261 (1857)
Typhonium reinwardtiana de Vriese & Miq. ex Miq. Fl. Ned. Ind. iii. 195.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Igbo Ọrịa na-acha uhie uhie
Malay keladi tikus
Malay pokok keladi tikus
Chinese 鞭檐犁头尖(水半夏)
Chinese 鞭檐犁头尖半夏
Chinese 疯狗薯
Chinese 鞭檐犁头尖
Chinese 半夏
Chinese 田三七
Chinese 水半夏

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!
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
      • Assam
      • Bangladesh
      • India
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000328908
UNII 001N5XW29X
Tropicos 2104570
KEW urn:lsid:ipni.org:names:89233-1
The Plant List kew-209474
Open Tree Of Life 300833
NCBI Taxonomy 458697
IUCN Red List 194754
IPNI 89233-1
iNaturalist 347760
GBIF 2869538
Freebase /m/0h7ql7c
EOL 1128159
Wikipedia Typhonium_flagelliforme
CMAUP NPO13898

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
CRISPR/Cas9: an advanced platform for root and tuber crops improvement Divya K, Thangaraj M, Krishna Radhika N Front Genome Ed 19-Jan-2024
PMCID:PMC10836405
doi:10.3389/fgeed.2023.1242510
PMID:38312197
Enhanced wedelolactone content in in vitro-raised genetically uniform Wedelia chinensis under the influence of CuSO4 Swami RK, Nimker S, Narula A, Farooqi H Front Plant Sci 19-Dec-2023
PMCID:PMC10758438
doi:10.3389/fpls.2023.1281445
PMID:38169740
In vitro cytotoxic effect of stigmasterol derivatives against breast cancer cells Dube NP, Tembu VJ, Nyemba GR, Davison C, Rakodi GH, Kemboi D, de la Mare JA, Siwe-Noundou X, Manicum AL BMC Complement Med Ther 11-Sep-2023
PMCID:PMC10496295
doi:10.1186/s12906-023-04137-y
PMID:37697361
Acute and Subchronic Oral Toxicity Evaluation of Herbal Formulation: Piper crocatum Ruiz and Pav., Typhonium flagelliforme (Lodd.) Blume, and Phyllanthus niruri L. in Sprague–Dawley Rats Murwanti R, Nurrochmad A, Gani AP, Sasmito E, Edwina AE, Chandra MK, Suryawan FH, Wardana AR, Natalia, Budiningsih JL J Toxicol 03-Jan-2023
PMCID:PMC9831695
doi:10.1155/2023/7511397
PMID:36636256
An Alternative In Vitro Propagation Protocol of Cannabis sativa L. (Cannabaceae) Presenting Efficient Rooting, for Commercial Production Ioannidis K, Tomprou I, Mitsis V Plants (Basel) 18-May-2022
PMCID:PMC9146626
doi:10.3390/plants11101333
PMID:35631759
Plant microbe based remediation approaches in dye removal: A review Gayathiri E, Prakash P, Selvam K, Awasthi MK, Gobinath R, Karri RR, Ragunathan MG, Jayanthi J, Mani V, Poudineh MA, Chang SW, Ravindran B Bioengineered 16-Mar-2022
PMCID:PMC9208495
doi:10.1080/21655979.2022.2049100
PMID:35294324
In Vitro Propagation, Genetic Assessment, and Medium-Term Conservation of the Coastal Endangered Species Tetraclinis articulata (Vahl) Masters (Cupressaceae) from Adult Trees Juan-Vicedo J, Serrano-Martínez F, Cano-Castillo M, Casas JL Plants (Basel) 11-Jan-2022
PMCID:PMC8778163
doi:10.3390/plants11020187
PMID:35050075
Ultrafast identification of Pinelliae Rhizoma using colorimetric direct-VPCR Chen R, Ding S, Wei Y, Yu J, Xu R, Luo X, Fan G, Yin H, Bian J 3 Biotech 15-Nov-2021
PMCID:PMC8593080
doi:10.1007/s13205-021-03035-9
PMID:34881156
The Efficient and Easy Micropropagation Protocol of Phyllanthus niruri Suraya AA, Misran A, Hakiman M Plants (Basel) 09-Oct-2021
PMCID:PMC8538876
doi:10.3390/plants10102141
PMID:34685949
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
Medicinal Plants with Anti-Leukemic Effects: A Review Maher T, Ahmad Raus R, Daddiouaissa D, Ahmad F, Adzhar NS, Latif ES, Abdulhafiz F, Mohammed A Molecules 07-May-2021
PMCID:PMC8124366
doi:10.3390/molecules26092741
PMID:34066963
Biotechnological Approaches on Two High CBD and CBG Cannabis sativa L. (Cannabaceae) Varieties: In Vitro Regeneration and Phytochemical Consistency Evaluation of Micropropagated Plants Using Quantitative 1H-NMR Ioannidis K, Dadiotis E, Mitsis V, Melliou E, Magiatis P Molecules 15-Dec-2020
PMCID:PMC7765244
doi:10.3390/molecules25245928
PMID:33333745
In vitro antiproliferation activity of Typhonium flagelliforme leaves ethanol extract and its combination with canine interferons on several tumor-derived cell lines Priosoeryanto BP, Rostantinata R, Harlina E, Nurcholis W, Ridho R, Sutardi LN Vet World 19-May-2020
PMCID:PMC7311872
doi:10.14202/vetworld.2020.931-939
PMID:32636590
Medicinal Plants in the Prevention and Treatment of Colon Cancer Aiello P, Sharghi M, Mansourkhani SM, Ardekan AP, Jouybari L, Daraei N, Peiro K, Mohamadian S, Rezaei M, Heidari M, Peluso I, Ghorat F, Bishayee A, Kooti W Oxid Med Cell Longev 04-Dec-2019
PMCID:PMC7187726
doi:10.1155/2019/2075614
PMID:32377288
Assessment of Phytoremediation Potential of Chara vulgaris to Treat Toxic Pollutants of Textile Effluent Mahajan P, Kaushal J, Upmanyu A, Bhatti J J Toxicol 03-Feb-2019
PMCID:PMC6377995
doi:10.1155/2019/8351272
PMID:30853979

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dodecane 8182 Click to see CCCCCCCCCCCC 170.33 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Eicosane 8222 Click to see CCCCCCCCCCCCCCCCCCCC 282.50 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Pentadecane 12391 Click to see CCCCCCCCCCCCCCC 212.41 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Tridecane 12388 Click to see CCCCCCCCCCCCC 184.36 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl 13-phenyltridecanoate 19792507 Click to see COC(=O)CCCCCCCCCCCCC1=CC=CC=C1 304.50 unknown https://doi.org/10.1055/S-2006-957778
Methyl oleate 5364509 Click to see CCCCCCCCC=CCCCCCCCC(=O)OC 296.50 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
> 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
13-phenyltridecanoic Acid 10541544 Click to see C1=CC=C(C=C1)CCCCCCCCCCCCC(=O)O 290.40 unknown https://doi.org/10.1016/S0378-8741(01)00274-4
https://doi.org/10.1055/S-2006-957778
> 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
Irehdiamine C 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
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
Regholarrhenine F 14543701 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)CO)N(C)C 388.60 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
(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
7-Hydroxyconessine 102093825 Click to see CC1C2CCC3C2(CCC4C3C(C=C5C4(CCC(C5)N(C)C)C)O)CN1C 372.60 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
Conkuressine 12303833 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
Regholarrhenine E 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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
Conarrhimine 12303820 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N)C)CN1 314.50 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
Regholarrhenine D 101529337 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1O 358.60 unknown via CMAUP database
> 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

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

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.