kalopanaxsaponin b (Q27137710)

Hederacoside C (English)

RYHDIBJJJRNDSX-SYAWYWTDSA-N

7 October 2016

stereoisomer of

2 references

RYHDIBJJJRNDSX-MQZKKVPJSA-N

2 references

RYHDIBJJJRNDSX-ADAPURKRSA-N

2 references

2 references

RYHDIBJJJRNDSX-SFRFVMPLSA-N

1 reference

RYHDIBJJJRNDSX-RCEFTJEHSA-N

1 reference

RYHDIBJJJRNDSX-KYLCFNLGSA-N

1 reference

chemical formula

C₅₉H₉₆O₂₆

1 reference

Hederacoside C (English)

20 November 2016

canonical SMILES

CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)O)O)O)CO)O)O)O

1 reference

Hederacoside C (English)

20 November 2016

isomeric SMILES

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)O)OC[C@@H]3[C@H]([C@@H]([C@H]([C@@H](O3)OC(=O)[C@@]45CC[C@@]6(C(=CC[C@H]7[C@]6(CC[C@@H]8[C@@]7(CC[C@@H]([C@@]8(C)CO)O[C@H]9[C@@H]([C@H]([C@H](CO9)O)O)O[C@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)C)O)O)O)C)C)[C@@H]4CC(CC5)(C)C)C)O)O)O)CO)O)O)O

1 reference

Kalopanax saponin B fromHedera caucasigena

Hederacoside C (English)

20 November 2016

2 references

Triterpene glycosides ofHedera caucasigena

Hedera pastuchovii

1 reference

Triterpene glycosides ofHedera Pastuchovii

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

A potent anti-diabetic agent from Kalopanax pictus

Metabolism of kalopanaxsaponin B and H by human intestinal bacteria and antidiabetic activity of their metabolites

Antifungal activity of modified hederagenin glycosides from the leaves of Kalopanax pictum var. chinense

Anti-inflammatory triterpenoid saponins 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.

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

Akebia trifoliata

1 reference

Triterpenes and triterpene saponins from the stems of Akebia trifoliata.

Anemone coronaria

1 reference

Triterpene glycosides from the tubers of Anemone coronaria

Clematis chinensis

1 reference

Triterpene saponins from Clematis chinensis and their potential anti-inflammatory activity.

Clematis orientalis

1 reference

Triterpene glycosides from Clematis orientalis

Clematis stans

1 reference

Studies on the constituents of Clematis species. VI. The constituents of Clematis stans Sieb. et Zucc

Clematis tibetana

1 reference

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

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 helix

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

Molecular complexation of α-hederin with hederasaponin C

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

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

In vitro antispasmodic compounds of the dry extract obtained from Hedera helix

Triterpenoid Saponins from the Leaves of Hedera helix

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

Hedera colchica

3 references

Triterpenoid saponins from berries of Hedera colchica

Arjunolic Acid Derivative Glycoside from the Stems of Hedera colchica

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

Hedera nepalensis

1 reference

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

Hedera taurica

1 reference

Molecular complexation of α-hederin with hederasaponin C

Oreopanax guatemalensis

1 reference

Triterpenoid saponins from Oreopanax guatemalensis.

Pulsatilla dahurica

1 reference

Chemical constituents of Pulsatilla dahurica

Pulsatilla cernua

1 reference

Triterpenoidal saponins of Pulsatilla koreana roots

Stauntonia chinensis

1 reference

Triterpenoid glycosides from Stauntonia chinensis

Hedera hibernica

4 references

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

In vitro antispasmodic compounds of the dry extract obtained from Hedera helix

Triterpenoid Saponins from the Leaves of Hedera helix

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

Pulsatilla chinensis

1 reference

Triterpene Glycosides from Pulsatilla chinensis

Acer pictum

5 references

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

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

Antifungal activity of modified hederagenin glycosides from the leaves of Kalopanax pictum var. chinense

A potent anti-diabetic agent from Kalopanax pictus

Metabolism of kalopanaxsaponin B and H by human intestinal bacteria and antidiabetic activity of their metabolites

Caltha palustris

1 reference

Two oleanene glycosides from the aerial parts of Caltha polypetala

Stauntonia hexaphylla

1 reference

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

Identifiers

InChI

InChI=1S/C59H96O26/c1-24-34(63)38(67)42(71)49(78-24)83-46-29(20-60)80-48(45(74)41(46)70)77-22-30-37(66)40(69)44(73)51(81-30)85-53(75)59-17-15-54(3,4)19-27(59)26-9-10-32-55(5)13-12-33(56(6,23-61)31(55)11-14-58(32,8)57(26,7)16-18-59)82-52-47(36(65)28(62)21-76-52)84-50-43(72)39(68)35(64)25(2)79-50/h9,24-25,27-52,60-74H,10-23H2,1-8H3/t24-,25-,27-,28-,29+,30+,31+,32+,33-,34-,35-,36-,37+,38+,39+,40-,41+,42+,43+,44+,45+,46+,47+,48+,49-,50-,51-,52-,55-,56-,57+,58+,59-/m0/s1

0 references

2 references

Hederacoside C (English)

20 November 2016

ChEBI release 2020-09-01

2 references

kalopanaxsaponin B (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=14216-03-6

8 April 2021

1 reference

6-Deoxy-alpha-L-mannopyranosyl-(1->4)-beta-D-glucopyranosyl-(1->6)-1-O-[(3beta)-3-{[2-O-(6-deoxy-alpha-L-mannopyranosyl)-alpha-L-arabinopyranosyl]oxy}-23-hydroxy-28-oxoolean-12-en-28-yl]-beta-D-glucop (English)

20 November 2016

2 references

Hederacoside C (English)

20 November 2016

Reaxys registry number

4229541

1 reference

kalopanaxsaponin B (English)

7 October 2016

ChEBI ID

69371

mapping relation type

2 references

KALOPANAXSAPONIN B (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C59H96O26/c1-24-34(63)38(67)42(71)49(78-24)83-46-29(20-60)80-48(45(74)41(46)70)77-22-30-37(66)40(69)44(73)51(81-30)85-53(75)59-17-15-54(3,4)19-27(59)26-9-10-32-55(5)13-12-33(56(6,23-61)31(55)11-14-58(32,8)57(26,7)16-18-59)82-52-47(36(65)28(62)21-76-52)84-50-43(72)39(68)35(64)25(2)79-50/h9,24-25,27-52,60-74H,10-23H2,1-8H3/t24-,25-,27-,28-,29+,30+,31+,32+,33-,34-,35-,36-,37+,38+,39+,40-,41+,42+,43+,44+,45+,46+,47+,48+,49-,50-,51-,52-,55-,56-,57+,58+,59-/m0/s1

1 reference

KALOPANAXSAPONIN B (English)

20 November 2016

1 reference

MassBank accession ID

MSBNK-RIKEN-PR301865

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

MassBank/MassBank-data: release version 2022.06 to wikidata

4 September 2022

1 reference

EC number

238-072-2

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.034.596

29 July 2019

ECHA Substance Infocard ID

Olean-12-en-28-oic acid, 3-[[2-O-(6-deoxy-α-l-mannopyranosyl)-α-l-arabinopyranosyl]oxy]-23-hydroxy-, O-6-deoxy-α-l-mannopyranosyl-(1→4)-O-β-d-glucopyranosyl-(1→6)-β-d-glucopyranosyl ester, (3β,4α)- (English)

quotation

CAS no.: 14216-03-6 (English)

100.034.596

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.034.596

29 July 2019

Olean-12-en-28-oic acid, 3-[[2-O-(6-deoxy-α-l-mannopyranosyl)-α-l-arabinopyranosyl]oxy]-23-hydroxy-, O-6-deoxy-α-l-mannopyranosyl-(1→4)-O-β-d-glucopyranosyl-(1→6)-β-d-glucopyranosyl ester, (3β,4α)- (English)

quotation

CAS no.: 14216-03-6 (English)

UNII

2608B2L1BQ

1 reference