(Q25105925)

English

α-hederin

chemical compound

alpha-hederin
kizutasaponin K6
akebiasaponin PD
tauroside E
glycoside L-E1
koronaroside A
hederoside C
prosapogenin CP3b
helixin
akeboside Stc
sapindoside A
3-O-alpha-L-rhamnopyranosyl-(1->2)-alpha-L-arabinopyranosyl hederagenin
alpha-Hederin
Helixin
Kalopanaxsaponin A
Kizuta saponin K6
Koronaroside A

In more languages

Statements

type of chemical entity

0 references

KEOITPILCOILGM-HYJPIGBRSA-N

1 reference

based on heuristic

inferred from SMILES

chemical structure

Alpha-hederin.svg
1,095 × 735; 77 KB

0 references

750.455±0 dalton

1 reference

language of work or name

alpha-Hederin (English)

7 October 2016

stereoisomer of

KEOITPILCOILGM-FDTCCIBYSA-N

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

KEOITPILCOILGM-IPOPOHETSA-N

1 reference

based on heuristic

inferred from InChI

KEOITPILCOILGM-DPHDLXGLSA-N

1 reference

based on heuristic

inferred from InChI

KEOITPILCOILGM-ATMJNGMXSA-N

1 reference

based on heuristic

inferred from InChI

KEOITPILCOILGM-WBRCRIAPSA-N

1 reference

based on heuristic

inferred from InChI

KEOITPILCOILGM-NUJXUPTKSA-N

1 reference

based on heuristic

inferred from InChI

KEOITPILCOILGM-FCWYPSSHSA-N

1 reference

based on heuristic

inferred from InChI

chemical formula

C₄₁H₆₆O₁₂

1 reference

language of work or name

alpha-Hederin (English)

19 November 2016

canonical SMILES

CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)O)O

1 reference

language of work or name

alpha-Hederin (English)

19 November 2016

isomeric SMILES

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@H](CO[C@H]2O[C@H]3CC[C@]4([C@H]([C@]3(C)CO)CC[C@@]5([C@@H]4CC=C6[C@]5(CC[C@@]7([C@H]6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)O)O

1 reference

language of work or name

alpha-Hederin (English)

19 November 2016

Eleutherococcus sieboldianus

2 references

Saponins from leaves of Acanthopanax sieboldianus

Triterpene glycosides from leaves ofAcanthopanax sieboldianus introduced to Ukraine and Crimea

Kalopanax septemlobus

7 references

Anti-inflammatory triterpenoid saponins from the stem bark of Kalopanax pictus

Saponins from leaves of Kalopanax pictum var. maximowiczii, a Korean medicinal plant

A potent anti-diabetic agent from Kalopanax pictus

Anti-inflammatory triterpenoid saponins from the stem bark of Kalopanax pictus

Essential moiety for antimutagenic and cytotoxic activity of hederagenin monodesmosides and bisdesmosides isolated from the stem bark of Kalopanax pictus.

Saponins from leaves of Kalopanax septemlobus (Thunb.) Koidz.: Structures of Kalopanax-saponins La, Lb and Lc.

Saponins from roots of Kalopanax septemlobus (THUNB.)KOIDZ., Ciqiu: Structures of kalopanax-saponins C, D, E and F.

1 reference

Kalopanaxsaponin A ameliorates experimental colitis in mice by inhibiting IRAK-1 activation in the NF-κB and MAPK pathways

Clematis tangutica

1 reference

Triterpenoid saponins from Clematis tangutica.

Clematis tibetana

2 references

Studies on the constituents of Clematis species. VIII. Triterpenoid saponins from the aerial part of Clematis tibetana KUNTZ.

Studies on the constituents of Clematis species. VIII. Triterpenoid saponins from the aerial part of Clematis tibetana KUNTZ.

Elattostachys apetala

2 references

Triterpenoid saponins from the stem bark of Elattostachys apetala

Triterpenoid saponins from the stem bark of Elattostachys apetala

Hedera colchica

3 references

Acute anti-inflammatory activity of four saponins isolated from ivy: alpha-hederin, hederasaponin-C, hederacolchiside-E and hederacolchiside-F in carrageenan-induced rat paw edema

Triterpenoid saponins from berries of Hedera colchica

Triterpenoid saponins from berries of Hedera colchica

3 references

Triterpene glycosides ofHedera taurica I. Structure of tauroside E from the leaves ofHedera taurica

Triterpene glycosides of Hedera taurica. V. Structure of hederosides C and E1 from Crimean ivy berries

Molecular complexation of α-hederin with hederasaponin C

2 references

Extraction, isolation and characterisation of antitumor principle, alpha-hederin, from the seeds of Nigella sativa

Extraction, isolation and characterisation of antitumor principle, alpha-hederin, from the seeds of Nigella sativa

Polyscias fulva

2 references

A new dammarane-type triterpene glycoside from Polyscias fulva

Constituents isolated from Polyscias fulva

Pulsatilla cernua

1 reference

Triterpenoid saponins from Pulsatilla cernua Spreng. I.

Sapindus delavayi

1 reference

Saponins of pericarps of Chinese Sapindus delavayi (Pyi-shiau-tzu), a source of natural surfactants.

Sapindus mukorossi

2 references

Saponins of pericarps of Sapindus mukurossi Gaertn. and solubilization of monodesmosides by bisdesmosides.

Triterpenoid saponins from the fruits and galls of Sapindus mukorossi

Pulsatilla chinensis

3 references

Triterpene saponins and lignans from the roots of Pulsatilla chinensis and their cytotoxic activity against HL-60 cells.

New bisdesmosidic triterpene saponins from the roots of Pulsatilla chinensis

Triterpene saponins and lignans from the roots of Pulsatilla chinensis and their cytotoxic activity against HL-60 cells.

Akebia trifoliata

1 reference

Antinociceptive and anti-inflammatory effects of the saponin and sapogenins obtained from the stem of Akebia quinata

3 references

Structure-activity relationship of oleanane disaccharides isolated from Akebia quinata versus cytotoxicity against cancer cells and NO inhibition

Triterpene glycosides from the stems of Akebia quinata

A triterpene glycoside and flavonoids from leaves of Akebia quinata

Anemoclema glaucifolium

1 reference

Triterpenoid glycosides from Anemoclema glaucifolium

Anemone coronaria

1 reference

Triterpene glycosides from the tubers of Anemone coronaria

Clematis orientalis

1 reference

Triterpene glycosides from Clematis orientalis

Hedera canariensis

3 references

Triterpene glycosides ofHedera canariensis. I. Structures of glycosides L-A, L-B1, L-B2, L-C, L-D, L-E1 1, L-G1, L-G2, L-G3, L-G4, L-H1, L-H2, AND L-I1 from the leaves ofHedera canariensis

Molecular complexation of α-hederin with hederasaponin C

Triterpene glycosides ofHedera canariensis. V. Structure of glycosides from canary ivy stems

Hedera caucasigena

1 reference

Triterpene glycosides fromHedera caucasignena leaves

Hedera nepalensis

1 reference

Studies on nepalese crude drugs. III. On the saponins of Hedera nepalensis K. Koch.

Lonicera japonica

1 reference

Studies on the saponins of Lonicera japonica THUNB

Medicago polymorpha

3 references

Isolation of a saponin, hederin, and its sapogenin, hederagenin, from bur clover (Medicago hispida)

Two new triterpenoidal glycosides from Medicago polymorpha L

Triterpenoid glycosides from the leaves of two cultivars of Medicago polymorpha L

Pulsatilla dahurica

1 reference

Chemical constituents of Pulsatilla dahurica

Anemone taipaiensis

1 reference

Bioactive oleanane-type saponins from the rhizomes of Anemone taipaiensis

Lonicera macrantha

1 reference

Triterpene glycosides from Lonicera. Isolation and structural determination of seven glycosides from flower buds of Lonicera macranthoides

4 references

A potent anti-diabetic agent from Kalopanax pictus

Anti-inflammatory triterpenoid saponins from the stem bark of Kalopanax pictus

Saponins from leaves of Kalopanax pictum var. maximowiczii, a Korean medicinal plant

Essential moiety for antimutagenic and cytotoxic activity of hederagenin monodesmosides and bisdesmosides isolated from the stem bark of Kalopanax pictus.

Stauntonia hexaphylla

1 reference

Bioactive triterpene glycosides from the fruit of Stauntonia hexaphylla and insights into the molecular mechanism of its inflammatory effects

8 references

Triterpene glycosides ofHedera canariensis. I. Structures of glycosides L-A, L-B1, L-B2, L-C, L-D, L-E1 1, L-G1, L-G2, L-G3, L-G4, L-H1, L-H2, AND L-I1 from the leaves ofHedera canariensis

Triterpene glycosides ofHedera canariensis. V. Structure of glycosides from canary ivy stems

Molecular complexation of α-hederin with hederasaponin C

Triterpene glycosides ofHedera helix I. The structures of glycosides L-1, L-2a, L-2b, L-3, L-4a, L-4b, L-6a, L-6b, L-6c, L-7a, and L7-b from the leaves of common ivy

High-performance liquid chromatographic determination of saponins fromHedera helix L. using a light-scattering detector

Alpha-hederin potentiates 5-FU antitumor activity in human colon adenocarcinoma cells

Saponins of the ivy plant, Hedera helix, and their leishmanicidic activity

What parts of fleshy fruits contain secondary compounds toxic to birds and why?

Identifiers

InChI=1S/C41H66O12/c1-21-28(44)30(46)31(47)33(51-21)53-32-29(45)24(43)19-50-34(32)52-27-11-12-37(4)25(38(27,5)20-42)10-13-40(7)26(37)9-8-22-23-18-36(2,3)14-16-41(23,35(48)49)17-15-39(22,40)6/h8,21,23-34,42-47H,9-20H2,1-7H3,(H,48,49)/t21-,23-,24-,25+,26+,27-,28-,29-,30+,31+,32+,33-,34-,37-,38-,39+,40+,41-/m0/s1

1 reference

language of work or name

alpha-Hederin (English)

19 November 2016

KEOITPILCOILGM-LLJOFIFVSA-N

2 references

language of work or name

alpha-Hederin (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

Global Substance Registration System

language of work or name

α-hederin (English)

19 November 2016

KEOITPILCOILGM-LLJOFIFVSA-N

CAS Common Chemistry

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=27013-91-8

1 reference

language of work or name

(3beta)-3-{[2-O-(6-Deoxy-alpha-L-mannopyranosyl)-alpha-L-arabinopyranosyl]oxy}-23-hydroxyolean-12-en-28-oic acid (English)

19 November 2016

1 reference

language of work or name

alpha-Hederin (English)

19 November 2016

Reaxys registry number

76156

1 reference

language of work or name

kalopanaxsaponin A (English)

7 October 2016

mapping relation type

1 reference

language of work or name

ALPHA-HEDERIN (English)

19 November 2016

1 reference

language of work or name

ALPHA-HEDERIN (English)

19 November 2016

UniChem compound ID

1 reference

MassBank accession ID

MSBNK-RIKEN-PR301873

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301874

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301875

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301876

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301877

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301878

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301879

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301880

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301881

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301882

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

MSBNK-RIKEN-PR301883

1 reference

KEOITPILCOILGM-LLJOFIFVSA-N

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

based on heuristic

DSSTox substance ID

0 references

0 references

DSSTOX compound identifier

DTXCID901377966

0 references

DTXCID101338235

0 references

0 references

248-166-5

1 reference

Global Substance Registration System

language of work or name

α-hederin (English)

19 November 2016

ECHA Substance Infocard ID

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

(4α)-3β-[[2-O-(6-deoxy-α-L-mannopyranosyl)-α-L-arabinopyranosyl]oxy]-23-hydroxyolean-12-en-28-oic acid (English)

CAS no.: 27013-91-8 (English)

1 reference

language of work or name

kalopanaxsaponin A (English)

7 October 2016

1 reference

Global Substance Registration System

language of work or name

α-hederin (English)

19 November 2016

Probes And Drugs ID

0 references

1 reference

language of work or name

kalopanaxsaponin A (English)

7 October 2016

Google Knowledge Graph ID

0 references

Sitelinks

Wikipedia(4 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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