Vincetoxicum hirundinaria subsp. hirundinaria

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Internal ID UUID644069946befd653374165
Scientific name Vincetoxicum hirundinaria subsp. hirundinaria
First published in Unknown

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Language Common/alternative name
English vincetoxicum hirundinaria hirundinaria
Spanish vincetoxicum hirundinaria hirundinaria
Bulgarian vincetoxicum hirundinaria hirundinaria
French vincetoxicum hirundinaria hirundinaria
Italian vincetoxicum hirundinaria hirundinaria
Russian vincetoxicum hirundinaria hirundinaria

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Distribution (via POWO/KEW) Top

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Database ID/link to page
World Flora Online wfo-0001425934
Tropicos 2610936
INPN 142268
Flora of Italy 4081
KEW urn:lsid:ipni.org:names:77173520-1
NCBI Taxonomy 2591842
GBIF 7312084

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
SPEKTROSKOPISCHE IDENTIFIZIERUNG VON C/6 UND C/7 IN<i>CYNANCHUM VINCETOXICUM</i> H.–W. Fehlhaber, G. Snatzke, L. Tóth, A. Háznagy, Zs. Makay Georg Thieme Verlag KG 15-Jan-2009
doi:10.1055/S-0028-1099825
BEITRAG ZU DEN UNTERSUCHUNGEN DER INHALTSSTOFFE VON<i>CYNANCHUM VINCETOXICUM</i>II<sup>1</sup> A. Háznagy, L. Tóth Georg Thieme Verlag KG 15-Jan-2009
doi:10.1055/S-0028-1099972
Alkaloide aus Vincetoxicum officinale Moench M. Pailer, W. Streicher Springer Science and Business Media LLC 02-Jan-2005
doi:10.1007/BF00919184
New phenatroindolizidine N-oxides alkaloids isolated from Vincetoxicum hirudinaria medic. M. Lavault, P. Richomme, J. Bruneton Elsevier BV 14-Dec-2002
doi:10.1016/0031-6865(94)90052-3
In vitro cytotoxic activity of phenanthroindolizidine alkaloids from Cynanchum vincetoxicum and Tylophora tanakae against drug-sensitive and multidrug-resistant cancer cells. Staerk D, Lykkeberg AK, Christensen J, Budnik BA, Abe F, Jaroszewski JW J Nat Prod 01-Sep-2002
doi:10.1021/NP0106384
PMID:12350151
Acetophenones and new pregnane glycosides from the roots of Vincetoxicum hirundinaria M Lavault, P Richomme, J Bruneton Elsevier BV 25-Jul-2002
doi:10.1016/S0367-326X(99)00023-4
Hancokinol from Vincetoxicum officinale. Nowak R, Kisiel W Fitoterapia 01-Sep-2000
doi:10.1016/S0367-326X(00)00157-X
PMID:11449515
Alkaloids of Cynanchum vincetoxicum: efficacy against MDA-MB-231 mammary carcinoma cells. Tanner U, Wiegrebe W Arch Pharm (Weinheim) 01-Feb-1993
doi:10.1002/ARDP.19933260203
PMID:8457148

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
> Benzenoids / Phenanthrenes and derivatives / Phenanthroindolizidines
(+/-)-Antofine 5316514 Click to see COC1=CC2=C(C=C1)C3=C(CC4CCCN4C3)C5=CC(=C(C=C52)OC)OC 363.40 unknown https://doi.org/10.1021/NP0106384
https://doi.org/10.1002/ARDP.19933260203
https://doi.org/10.1007/BF00919184
(+/-)-Tylophorine 5090648 Click to see COC1=C(C=C2C(=C1)C3=C(CN4CCCC4C3)C5=CC(=C(C=C52)OC)OC)OC 393.50 unknown https://doi.org/10.1002/ARDP.19933260203
(13aR)-2,3-dimethoxy-9,11,12,13,13a,14-hexahydrophenanthro[10,9-f]indolizin-6-ol 9975115 Click to see COC1=C(C=C2C(=C1)C3=C(CN4CCCC4C3)C5=C2C=C(C=C5)O)OC 349.40 unknown https://doi.org/10.1021/NP0106384
(13aR)-2,3,6-trimethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine 639288 Click to see COC1=CC2=C(C=C1)C3=C(CC4CCCN4C3)C5=CC(=C(C=C52)OC)OC 363.40 unknown https://doi.org/10.1016/0031-6865(94)90052-3
https://doi.org/10.1021/NP0106384
https://doi.org/10.1007/BF00919184
https://doi.org/10.1002/ARDP.19933260203
2,3-Dimethoxy-9,11,12,13,13a,14-hexahydrophenanthro[10,9-f]indolizin-6-ol 16656775 Click to see COC1=C(C=C2C(=C1)C3=C(CN4CCCC4C3)C5=C2C=C(C=C5)O)OC 349.40 unknown https://doi.org/10.1002/ARDP.19933260203
https://doi.org/10.1021/NP0106384
Tylophorine 92114 Click to see COC1=C(C=C2C(=C1)C3=C(CN4CCCC4C3)C5=CC(=C(C=C52)OC)OC)OC 393.50 unknown https://doi.org/10.1002/ARDP.19933260203
Tylophorine, (-)- 10883727 Click to see COC1=C(C=C2C(=C1)C3=C(CN4CCCC4C3)C5=CC(=C(C=C52)OC)OC)OC 393.50 unknown https://doi.org/10.1002/ARDP.19933260203
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(1-Hydroxyethyl)phenol 102803 Click to see CC(C1=CC=C(C=C1)O)O 138.16 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1099825
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1099825
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Delta-5-steroids
Hancolupenone 195724 Click to see CC(C)C1CCC2(C1C3(CC=C4C(C3(CC2)C)CCC5C4(CCC(=O)C5(C)C)C)C)C 424.70 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
> 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/S0367-326X(99)00023-4
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/S0367-326X(99)00023-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid 7067333 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1055/S-0028-1099972
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1055/S-0028-1099972
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0367-326X(00)00157-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(4S,5R,8S,13R,19R,22R)-8-[(2R,4R,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2R,4R,5R,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 102071873 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3CCC4(C5CCC6=COC7(C6C(CO7)OC(=O)C5CC=C4C3)C)C)C)O)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC 941.10 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
(4S,5R,8S,13R,19R,22R)-8-[(2R,4R,5R,6R)-5-[(4S,5S,6R)-4-hydroxy-5-[(4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 102143205 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3OC)OC4CCC5(C6CCC7=COC8(C7C(CO8)OC(=O)C6CC=C5C4)C)C)C)C)OC)O 778.90 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2-Hydroxyacetophenone 68490 Click to see C1=CC=C(C=C1)C(=O)CO 136.15 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
Acetovanillone 2214 Click to see CC(=O)C1=CC(=C(C=C1)O)OC 166.17 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
Paeonol 11092 Click to see CC(=O)C1=C(C=C(C=C1)OC)O 166.17 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see COC1=C2C(=C(C(=C1)CC=C)OC)OCO2 222.24 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
Myristicin 4276 Click to see COC1=CC(=CC2=C1OCO2)CC=C 192.21 unknown https://doi.org/10.1016/S0367-326X(99)00023-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Sinapic acid 10743 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1055/S-0028-1099972
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1055/S-0028-1099972
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0367-326X(00)00157-X
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/S0367-326X(00)00157-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0367-326X(00)00157-X
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0367-326X(00)00157-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Vincetoxicoside B 5748601 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0367-326X(00)00157-X

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