(Q72493261)

English

Morusinol

chemical compound

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Statements

type of chemical entity

0 references

3,8C-substituted flavone

0 references

438.167853172 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₂₅H₂₆O₇

0 references

canonical SMILES

CC1(C=CC2=C(O1)C=C(C3=C2OC(=C(C3=O)CCC(C)(C)O)C4=C(C=C(C=C4)O)O)O)C

0 references

Morus australis

3 references

[Components of Root Bark of Morus australis.].

Kuwanon A, B, C and oxydihydromorusin, four new flavones from the root bark of the cultivated mulberry tree (Morus alba L.).

Cytotoxic flavonoids with isoprenoid groups from Morus mongolica

Morus mongolica

3 references

Cytotoxic flavonoids with isoprenoid groups from Morus mongolica

Kuwanon A, B, C and oxydihydromorusin, four new flavones from the root bark of the cultivated mulberry tree (Morus alba L.).

[Components of Root Bark of Morus australis.].

3 references

Inhibition and structural reliability of prenylated flavones from the stem bark of Morus lhou on β-secretase (BACE-1).

Tyrosinase inhibitory polyphenols from roots of Morus lhou.

Isolation of cholinesterase-inhibiting flavonoids from Morus lhou

8 references

Isolation of cholinesterase-inhibiting flavonoids from Morus lhou

Inhibition and structural reliability of prenylated flavones from the stem bark of Morus lhou on β-secretase (BACE-1).

Tyrosinase inhibitory polyphenols from roots of Morus lhou.

Evaluation of anti-inflammatory activity of prenylated substances isolated from Morus alba and Morus nigra

Antiviral flavonoids from the root bark of Morus alba L.

Kuwanon A, B, C and oxydihydromorusin, four new flavones from the root bark of the cultivated mulberry tree (Morus alba L.).

Cytotoxic flavonoids with isoprenoid groups from Morus mongolica

[Components of Root Bark of Morus australis.].

3 references

Cytotoxic flavonoids with isoprenoid groups from Morus mongolica

Kuwanon A, B, C and oxydihydromorusin, four new flavones from the root bark of the cultivated mulberry tree (Morus alba L.).

[Components of Root Bark of Morus australis.].

Identifiers

InChI=1S/C25H26O7/c1-24(2,30)9-7-16-21(29)20-18(28)12-19-15(8-10-25(3,4)32-19)23(20)31-22(16)14-6-5-13(26)11-17(14)27/h5-6,8,10-12,26-28,30H,7,9H2,1-4H3

0 references

AFOKZNPZDXHDHD-UHFFFAOYSA-N

0 references

CAS Registry Number

1 reference

AFOKZNPZDXHDHD-UHFFFAOYSA-N

CAS Common Chemistry

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=62949-93-3

1 reference

matched by identifier from

AFOKZNPZDXHDHD-UHFFFAOYSA-N

mapping relation type

2 references

ChEBI release 2022-06-13

matched by identifier from

International Chemical Identifier

InChI=1S/C25H26O7/c1-24(2,30)9-7-16-21(29)20-18(28)12-19-15(8-10-25(3,4)32-19)23(20)31-22(16)14-6-5-13(26)11-17(14)27/h5-6,8,10-12,26-28,30H,7,9H2,1-4H3

UniChem compound ID

1 reference

DSSTox substance ID

1 reference

matched by identifier from

AFOKZNPZDXHDHD-UHFFFAOYSA-N

DSSTOX compound identifier

0 references

Human Metabolome Database ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

AFOKZNPZDXHDHD-UHFFFAOYSA-N

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

AFOKZNPZDXHDHD-UHFFFAOYSA-N

1 reference

matched by identifier from

AFOKZNPZDXHDHD-UHFFFAOYSA-N

Probes And Drugs ID

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

30 June 2018

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Multilingual sites(0 entries)

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