(Q27107539)

inferred from SMILES

mass

408.142 dalton

1 reference

(2R)-2-[2-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one

Nodakenin (English)

5 October 2016

2 references

inferred from InChIKey

2 references

inferred from InChIKey

(2S)-2-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₀H₂₄O₉

1 reference

Nodakenin (English)

20 November 2016

CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O

1 reference

Nodakenin (English)

20 November 2016

CC(C)([C@H]1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O

1 reference

Nodakenin (English)

20 November 2016

Hansenia weberbaueriana

2 references

"Chemical studies on the constituents of the Chinese crude drug \"Quiang Huo\"."

Isolation of two new coumarin glycosides from Notopterygium forbesii and evaluation of a Chinese crude drug, qiang-huo, the underground parts of N. incisum and N. forbesii, by high-performance liquid chromatography

Hansenia forbesii

3 references

"Chemical studies on the constituents of the Chinese crude drug \"Quiang Huo\"."

Isolation of two new coumarin glycosides from Notopterygium forbesii and evaluation of a Chinese crude drug, qiang-huo, the underground parts of N. incisum and N. forbesii, by high-performance liquid chromatography

Isolation of two new coumarin glycosides from Notopterygium forbesii and evaluation of a Chinese crude drug, qiang-huo, the underground parts of N. incisum and N. forbesii, by high-performance liquid chromatography

Angelica gigas

5 references

Gigasol and other coumarins from Angelica gigas

Coumarins isolated from Angelica gigas inhibit acetylcholinesterase: structure-activity relationships

Coumarins isolated from Angelica gigas inhibit acetylcholinesterase: structure-activity relationships

Coumarins isolated from Angelica gigas inhibit acetylcholinesterase: structure-activity relationships

The simultaneous determination of coumarins in Angelica gigas root by high performance liquid chromatography-diode array detector coupled with electrospray ionization/mass spectrometry

Angelica dahurica

3 references

Coumarins of the roots of Angelica dahurica

Coumarin glycosides from the roots ofAngelica dahurica

Coumarins of the roots of Angelica dahurica

Angelica pubescens

1 reference

Inhibitory effects of Angelica pubescens f. biserrata on 5-lipoxygenase and cyclooxygenase

celery

2 references

Furanocoumarin glucosides from the seeds of Apium graveolens

Coumarins from Apium graveolens seeds

Kitagawia praeruptora

1 reference

Structures of glycosides of bai-hua quan-hu1

Cicuta virosa

1 reference

Coumarins from Cicuta virosa and their modulating effects on multidrug-resistant (MDR) tumors

Rhodiola rosea

1 reference

Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis

Rhodiola sachalinensis

1 reference

Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis

Angelica capitellata

1 reference

Coumarins IX: Coumarins of Sphenosciadium Capitellatum (A. Gray)

Halosciastrum melanotilingia

1 reference

Effect of Oriental Plant Drugs on Platelet Aggregation II1. Effect of Qian-Hu Coumarins on Human Platelet Aggregation

Angelica decursiva

4 references

Coumarins from "Zi-Hua Qian-Hu" (supplement)

Coumarins from the Roots of Angelica morii HAYATA

Studies on Coumarins of a Chinese Drug “Qian-Hu”; VII1. Structures of New Coumarin-Glycosides of Zi-Huan Quian-Hu and Effect of Coumarin-Glycosides on Human Platelet Aggregation

Studies on coumarins of a chinese drug "Qian-Hu"

Identifiers

InChI

InChI=1S/C20H24O9/c1-20(2,29-19-18(25)17(24)16(23)13(8-21)28-19)14-6-10-5-9-3-4-15(22)27-11(9)7-12(10)26-14/h3-5,7,13-14,16-19,21,23-25H,6,8H2,1-2H3/t13-,14-,16-,17+,18-,19+/m1/s1

1 reference

Nodakenin (English)

20 November 2016

2 references

Nodakenin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

495-31-8

2 references

Global Substance Registration System

UNII

S2KTH28M3N

nodakenin (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=495-31-8

9 April 2021

1 reference

Nodakenin (English)

20 November 2016

1 reference

Nodakenin (English)

20 November 2016

mapping relation type

2 references

English

NODAKENIN (English)

matched by identifier from

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C20H24O9/c1-20(2,29-19-18(25)17(24)16(23)13(8-21)28-19)14-6-10-5-9-3-4-15(22)27-11(9)7-12(10)26-14/h3-5,7,13-14,16-19,21,23-25H,6,8H2,1-2H3/t13-,14-,16-,17+,18-,19+/m1/s1

1 reference

MSBNK-Univ_Toyama-TY000089

NODAKENIN (English)

20 November 2016

1 reference

MassBank accession ID

0 references

MSBNK-Univ_Toyama-TY000202

0 references

MSBNK-Univ_Toyama-TY000203

0 references

SPLASH

splash10-014i-0000900010-4e8ead73a476905a6f44

0 references

splash10-004i-0090100000-c3aede6e89844ea681df

0 references

DSSTox substance ID

DTXSID601318602

1 reference

matched by identifier from

InChIKey

EC number

683-098-3

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.618

27 December 2018

ECHA Substance Infocard ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 495-31-8 (English)

100.208.618

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.618

27 December 2018

[No public or meaningful name is available] (English)

quotation

CAS no.: 495-31-8 (English)

1 reference

Global Substance Registration System

Nodakenin (English)

5 October 2016

2 references

UNII

S2KTH28M3N

English

nodakenin (English)

matched by identifier from

20 November 2016

InChIKey

0 references

1 reference

English

Nodakenin (English)