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Ancistrocladus tanzaniensis

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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 UUID64403c9ecb0de513549091
Scientific name Ancistrocladus tanzaniensis
Authority Cheek & Frim.-Møll.
First published in Kew Bull. 55: 207 (2000)

Description Top

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Synonyms Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000970471
Tropicos 50177236
KEW urn:lsid:ipni.org:names:1013853-1
The Plant List kew-8777
Open Tree Of Life 784339
NCBI Taxonomy 714107
IUCN Red List 158276
IPNI 1013853-1
iNaturalist 946356
GBIF 3659011
EOL 6874719

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
Computational study to discover potent phytochemical inhibitors against drug target, squalene synthase from Leishmania donovani Wadanambi PM, Mannapperuma U Heliyon 31-May-2021
PMCID:PMC8188062
doi:10.1016/j.heliyon.2021.e07178
PMID:34141935
Prevention of SARS-CoV-2 cell entry: insight from in silico interaction of drug-like alkaloids with spike glycoprotein, human ACE2, and TMPRSS2 Gyebi GA, Adegunloye AP, Ibrahim IM, Ogunyemi OM, Afolabi SO, Ogunro OB J Biomol Struct Dyn 22-Oct-2020
PMCID:PMC7594191
doi:10.1080/07391102.2020.1835726
PMID:33089728
Potential inhibitors of coronavirus 3-chymotrypsin-like protease (3CLpro): an in silico screening of alkaloids and terpenoids from African medicinal plants Gyebi GA, Ogunro OB, Adegunloye AP, Ogunyemi OM, Afolabi SO J Biomol Struct Dyn 18-May-2020
PMCID:PMC7256353
doi:10.1080/07391102.2020.1764868
PMID:32367767
Compounds from African Medicinal Plants with Activities Against Selected Parasitic Diseases: Schistosomiasis, Trypanosomiasis and Leishmaniasis Simoben CV, Ntie-Kang F, Akone SH, Sippl W Nat Prod Bioprospect 09-May-2018
PMCID:PMC5971035
doi:10.1007/s13659-018-0165-y
PMID:29744736
Plant-derived compounds in treatment of leishmaniasis Oryan A Iran J Vet Res 01-Jan-2015
PMCID:PMC4789233
PMID:27175144
The potential of anti-malarial compounds derived from African medicinal plants, part I: a pharmacological evaluation of alkaloids and terpenoids Amoa Onguéné P, Ntie-Kang F, Lifongo LL, Ndom JC, Sippl W, Mbaze LM Malar J 13-Dec-2013
PMCID:PMC3878730
doi:10.1186/1475-2875-12-449
PMID:24330395
Ancistrotanzanine C and related 5,1'- and 7,3'-coupled naphthylisoquinoline alkaloids from Ancistrocladus tanzaniensis. Bringmann G, Dreyer M, Faber JH, Dalsgaard PW, Staerk D, Jaroszewski JW, Ndangalasi H, Mbago F, Brun R, Christensen SB J Nat Prod 01-May-2004
doi:10.1021/NP0340549
PMID:15165131
Ancistrotanzanine A, the first 5,3'-coupled naphthylisoquinoline alkaloid, and two further, 5,8'-linked related compounds from the newly described species Ancistrocladus tanzaniensis. Bringmann G, Dreyer M, Faber JH, Dalsgaard PW, Staerk D, Jaroszewski JW, Ndangalasi H, Mbago F, Brun R, Reichert M, Maksimenka K, Christensen SB J Nat Prod 01-Sep-2003
doi:10.1021/NP030077B
PMID:14510589

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
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1R,3R)-5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-6,8-dimethoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinoline 163070817 Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)OC)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 435.60 unknown https://doi.org/10.1021/NP0340549
(1S,3S)-5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-6,8-dimethoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinoline 11224334 Click to see CC1CC2=C(C(=CC(=C2C(N1C)C)OC)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 435.60 unknown https://doi.org/10.1021/NP0340549
(3R)-7-[5-hydroxy-2-(hydroxymethyl)-4-methoxynaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 375947 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)O)O 379.40 unknown https://doi.org/10.1021/NP030077B
1,3-Dimethyl-6,8-dimethoxy-5-(4,5-dimethoxy-7-methyl-1-naphthyl)-3,4-dihydroisoquinoline 21589700 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 419.50 unknown https://doi.org/10.1021/NP030077B
2-(6,8-Dimethoxy-1,3-dimethyl-3,4-dihydroisoquinolin-5-yl)-8-methoxy-3-methylnaphthalen-1-ol 21589699 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O 405.50 unknown https://doi.org/10.1021/NP030077B
https://doi.org/10.1021/NP0340549
2-[(1R,3R)-6,8-dimethoxy-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-7-yl]-8-methoxy-3-methylnaphthalen-1-ol 162848346 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC 421.50 unknown https://doi.org/10.1021/NP0340549
2-[(3R)-6,8-dimethoxy-1,3-dimethyl-3,4-dihydroisoquinolin-7-yl]-8-methoxy-3-methylnaphthalen-1-ol 162900057 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC 405.50 unknown https://doi.org/10.1021/NP0340549
Ancistrocladidine 193880 Click to see CC1CC2=CC(=C(C(=C2C(=N1)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC 405.50 unknown https://doi.org/10.1021/NP0340549
Ancistrocladine 161741 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)O)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 407.50 unknown https://doi.org/10.1021/NP0340549
Ancistrotanzanine A 10319100 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O 405.50 unknown https://doi.org/10.1021/NP030077B
https://doi.org/10.1021/NP0340549
ancistrotanzanine B 10002166 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 419.50 unknown https://doi.org/10.1021/NP030077B
https://doi.org/10.1021/NP0340549
Ancistrotanzanine C 11350305 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)O 407.50 unknown https://doi.org/10.1021/NP0340549
Ancistrotectoriline A 10093654 Click to see CC1CC2=C(C(=CC(=C2C(N1)C)OC)OC)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C 421.50 unknown https://doi.org/10.1021/NP030077B
https://doi.org/10.1021/NP0340549
Ancistrotectorine 179169 Click to see CC1CC2=CC(=C(C(=C2C(N1C)C)OC)C3=C(C4=C(C=CC=C4OC)C=C3C)O)OC 421.50 unknown https://doi.org/10.1021/NP0340549
O-Methylancistrocladinine 11212280 Click to see CC1CC2=C(C(=CC(=C2C(=N1)C)OC)OC)C3=C4C=CC=C(C4=C(C=C3C)OC)OC 419.50 unknown https://doi.org/10.1021/NP0340549

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