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Scadoxus multiflorus subsp. multiflorus

Scadoxus multiflorus subsp. multiflorus - 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 UUID644026a27efc1889073822
Scientific name Scadoxus multiflorus subsp. multiflorus
First published in Unknown

Description Top

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Common names Top

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Language Common/alternative name
English blood-flower
English scadoxus multiflorus multiflorus
Spanish scadoxus multiflorus multiflorus
Bulgarian scadoxus multiflorus multiflorus
French scadoxus multiflorus multiflorus
Italian scadoxus multiflorus multiflorus
Russian scadoxus multiflorus multiflorus

Varieties (abbr. var.) 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

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000770511
USDA Plants SCMUM2
Tropicos 1200866
KEW urn:lsid:ipni.org:names:77171667-1
iNaturalist 514382
GBIF 7227603
USDA GRIN 412332

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)!
Title Authors Publication Released IDs
ALKALOIDS FROM HAEMANTHUS MULTIFLORUS MARTYN A. Ali, H. Sayed, O. Abdalla, W. Steglich, E. Dagne Egypts Presidential Specialized Council for Education and Scientific Research 03-Mar-2020
doi:10.21608/BFSA.1987.74054
Alkaloide von <i>Haemanthus multiflorus</i> Hans‐G. Boit, Werner Döpke Wiley 02-Jun-2007
doi:10.1002/CBER.19580910928
Haemultine and the Alkaloids of Haemanthus multiflorus Martyn<sup>1</sup> H. M. FALES, W. C. WILDMAN American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/JO01064A076
Alkaloids of Haemanthus kalbreyeri Shibnath Ghosal, Rajiv Lochan, Ashutosh Yatendra Kumar, Radhey S. Srivastava Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82560-1
Isocarbostyril alkaloids from Haemanthus kalbreyeri Shibnath Ghosal, Shripati Singh, Yatendra Kumar, Radhey S. Srivastava Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80061-5
2-O-acetyl chlidanthine; An alkaloid from Haemanthus multiflorus O.M. Abdallah, A.A. Ali, H. Itokawa Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80322-X

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
(-)-Montanine 11087935 Click to see COC1C=C2C(CC1O)N3CC2C4=CC5=C(C=C4C3)OCO5 301.34 unknown https://doi.org/10.1021/JO01064A076
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1S,11R,13S,15S,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 49799009 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/0031-9422(89)80061-5
https://doi.org/10.1016/S0031-9422(00)82560-1
(1S,11S,13S,15S,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 154496716 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1002/CBER.19580910928
(1S,13S,15S,18S)-15-Methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 5282090 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1016/0031-9422(89)80061-5
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1016/0031-9422(89)80061-5
Haemanthamine 441593 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1016/0031-9422(89)80061-5
Haemanthidine 544807 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1002/CBER.19580910928
https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1016/0031-9422(89)80061-5
Hemanthidine 3002914 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown https://doi.org/10.1016/0031-9422(89)80061-5
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(9-Hydroxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-yl) acetate 14413745 Click to see CC(=O)OC1CC2C3(CCN(CC4=C3C(=C(C=C4)O)O2)C)C=C1 315.40 unknown https://doi.org/10.1016/0031-9422(89)80322-X
[(1R,12S,14R)-9-hydroxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-yl] acetate 14413746 Click to see CC(=O)OC1CC2C3(CCN(CC4=C3C(=C(C=C4)O)O2)C)C=C1 315.40 unknown https://doi.org/10.1016/0031-9422(89)80322-X
Epigalanthamin 3449 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.1016/0031-9422(89)80322-X
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.1016/0031-9422(89)80322-X
https://doi.org/10.21608/BFSA.1987.74054
Sanguinine 443722 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)O)O 273.33 unknown https://doi.org/10.21608/BFSA.1987.74054
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1016/0031-9422(89)80061-5
https://doi.org/10.1016/0031-9422(89)80322-X
https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.21608/BFSA.1987.74054
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
(2R,3R,4S,4aR)-2,3,4,7-tetrahydroxy-3,4,4a,5-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 51351537 Click to see C1OC2=C(O1)C(=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O)O 307.25 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
1,2,3,4,7-pentahydroxy-2,3,4,4a,5,11b-hexahydro-1H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 609635 Click to see C1OC2=C(O1)C(=C3C(=C2)C4C(C(C(C(C4O)O)O)O)NC3=O)O 325.27 unknown https://doi.org/10.1016/0031-9422(89)80061-5
2,3,4-trihydroxy-3,4,4a,5-tetrahydro-2H-[1,3]dioxolo[4,5-j]phenanthridin-6-one 434381 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O 291.26 unknown https://doi.org/10.1016/0031-9422(89)80061-5
Kalbreclasine 441595 Click to see C1OC2=C(O1)C(=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 469.40 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
Lycoricidin-A 619061 Click to see C1OC2=C(O1)C(=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O)O 307.25 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1016/0031-9422(89)80061-5
Pancratistatin 441597 Click to see C1OC2=C(O1)C(=C3C(=C2)C4C(C(C(C(C4O)O)O)O)NC3=O)O 325.27 unknown https://doi.org/10.1016/0031-9422(89)80061-5
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
6-Hydroxy-7,8-dimethoxy-2-(2-oxopropyl)-2,3,3a,9b-tetrahydrofuro[3,2-c]isochromen-5-one 71436822 Click to see CC(=O)CC1CC2C(O1)C3=CC(=C(C(=C3C(=O)O2)O)OC)OC 322.31 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1016/0031-9422(89)80061-5
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
N-[1-(5-hydroxy-6-methyloxan-2-yl)-2-oxopyrimidin-4-yl]-3-methylbut-2-enamide 163061909 Click to see CC1C(CCC(O1)N2C=CC(=NC2=O)NC(=O)C=C(C)C)O 307.34 unknown https://doi.org/10.1021/JO01064A076
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1R,13S,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 15559601 Click to see C1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 271.31 unknown https://doi.org/10.1016/0031-9422(89)80322-X
(1S,13S,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,15-tetraen-18-ol 163085333 Click to see C1C=CCC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5 271.31 unknown https://doi.org/10.1002/CBER.19580910928
https://doi.org/10.1021/JO01064A076
(1S,13S,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 163006622 Click to see C1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 271.31 unknown https://doi.org/10.1021/JO01064A076
https://doi.org/10.1002/CBER.19580910928
11-Hydroxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-1(18),2,4(8),10,13,15(19),16-heptaen-9-one 135410291 Click to see C1OC2=C(O1)C(=O)C3=C(N4C=CC5=C4C(=CC=C5)C3=C2)O 279.25 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1016/0031-9422(89)80061-5
2,3-Didehydrocrinan-11-ol 623203 Click to see C1C=CCC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5 271.31 unknown https://doi.org/10.1002/CBER.19580910928
https://doi.org/10.1021/JO01064A076
Hemultine 614954 Click to see C1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 271.31 unknown https://doi.org/10.1002/CBER.19580910928
https://doi.org/10.1021/JO01064A076
https://doi.org/10.1016/0031-9422(89)80322-X
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1016/0031-9422(89)80322-X
Lycoricidine 73065 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O 291.26 unknown https://doi.org/10.1016/0031-9422(89)80061-5
Narciclasine 72376 Click to see C1OC2=C(O1)C(=C3C(=C2)C4=CC(C(C(C4NC3=O)O)O)O)O 307.25 unknown https://doi.org/10.1016/S0031-9422(00)82560-1
https://doi.org/10.1016/0031-9422(89)80061-5
Pratorimine 181937 Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O 265.26 unknown https://doi.org/10.1016/S0031-9422(00)82560-1

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