caprylyl glucoside (Q7077127)

octyl beta-L-talopyranoside

29836-26-8 (English)

19 October 2016

2 references

inferred from InChIKey

octyl alpha-L-altropyranoside

1 reference

octyl alpha-D-glucopyranoside

1 reference

octyl beta-D-galactopyranoside

1 reference

chemical formula

C₁₄H₂₈O₆

1 reference

29836-26-8 (English)

20 November 2016

CCCCCCCCOC1C(C(C(C(O1)CO)O)O)O

1 reference

29836-26-8 (English)

20 November 2016

CCCCCCCCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O

1 reference

29836-26-8 (English)

20 November 2016

Rhodiola sachalinensis

4 references

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

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

Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis

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

Rhodiola rosea

3 references

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis

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

Eucalyptus globulus

1 reference

Eucalyptone G, a new phloroglucinol derivative and other constituents from Eucalyptus globulus Labill

Identifiers

InChI

InChI=1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14-/m1/s1

1 reference

29836-26-8 (English)

20 November 2016

2 references

29836-26-8 (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

29836-26-8

2 references

caprylyl glucoside (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=29836-26-8

9 April 2021

1 reference

Octyl beta-D-glucopyranoside (English)

20 November 2016

2 references

29836-26-8 (English)

20 November 2016

ChEBI ID

41128

mapping relation type

exact match

2 references

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14-/m1/s1

1 reference

CHEMBL446037 (English)

20 November 2016

2 references

inferred from InChIKey

splash10-000j-9500000000-01ea4d2e9f4221372a2d

1 reference

0 references

DSSTox substance ID

DTXSID6042234

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

DTXCID4022234

0 references

EC number

249-887-8

1 reference

caprylyl glucoside (English)

ECHA Substance Infocard ID

20 November 2016

100.045.337

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.045.337

27 December 2018

AICS Chemical ID (BEING DELETED)

1-O-octyl-β-D-glucopyranoside (English)

quotation

CAS no.: 29836-26-8 (English)

1 reference

28 December 2019

CAPRYLYL GLUCOSIDE (English)

quotation

CAS no.: 29836-26-8 (English)

0 references

1 reference

Medical Subject Headings

14 March 2018

1 reference

caprylyl glucoside (English)

20 November 2016

2 references

caprylyl glucoside (English)

20 November 2016