(Q104400030)

English

Angelol G

chemical compound

In more languages

Statements

type of chemical entity

0 references

[2,3-dihydroxy-1-(7-methoxy-2-oxochromen-6-yl)-3-methylbutyl] (Z)-2-methylbut-2-enoate

1 reference

based on heuristic

inferred from SMILES

[2,3-Dihydroxy-1-(7-methoxy-2-oxochromen-6-yl)-3-methylbutyl] 2-methylbut-2-enoate

1 reference

based on heuristic

inferred from SMILES

376.152203108 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

[(1S,2S)-2,3-dihydroxy-1-(7-methoxy-2-oxochromen-6-yl)-3-methylbutyl] (E)-2-methylbut-2-enoate

1 reference

based on heuristic

inferred from InChIKey

1 reference

based on heuristic

inferred from InChIKey

1 reference

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

[(1S,2S)-2,3-dihydroxy-1-(7-methoxy-2-oxochromen-6-yl)-3-methylbutyl] (Z)-2-methylbut-2-enoate

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₀H₂₄O₇

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canonical SMILES

O=C1OC=2C=C(OC)C(=CC2C=C1)C(OC(=O)C(=CC)C)C(O)C(O)(C)C

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isomeric SMILES

C/C=C(/C)C(=O)O[C@H](c1cc2ccc(=O)oc2cc1OC)[C@@H](O)C(C)(C)O

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Campylotropis hirtella

1 reference

Coumarins from campylotropis hirtella (FRANCH.) SCHINDL. and their inhibitory activity on prostate specific antigen secreted from LNCaP cells

Angelica pubescens

2 references

Angelol-type coumarins from Angelica pubescence F. biserrata and their inhibitory effect on platelet aggregation

Anti-inflammatory and analgesic activities from roots of Angelica pubescens

Identifiers

InChI=1S/C20H24O7/c1-6-11(2)19(23)27-17(18(22)20(3,4)24)13-9-12-7-8-16(21)26-14(12)10-15(13)25-5/h6-10,17-18,22,24H,1-5H3/b11-6-/t17-,18-/m1/s1

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BAHUBXAYVOCLNA-FNYRBRLGSA-N

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2 references

17 September 2022

based on heuristic

inferred from InChIKey

matched by identifier from

BAHUBXAYVOCLNA-FNYRBRLGSA-N

UniChem compound ID

1 reference

Sitelinks

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