(Q104888799)

Methyl 3-(3,4-dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoate

inferred from SMILES

1 reference

inferred from SMILES

mass

374.100167536 dalton

1 reference

Rosmarinic Acid Methyl Ester

inferred from SMILES

stereoisomer of

2 references

inferred from InChIKey

(S)-3-(3,4-Dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (E)-3-(3,4-dihydroxyphenyl)acrylate

inferred from InChI

2 references

inferred from InChIKey

inferred from InChI

chemical formula

C₁₉H₁₈O₈

0 references

canonical SMILES

O=C(OC(C(=O)OC)CC1=CC=C(O)C(O)=C1)C=CC2=CC=C(O)C(O)=C2

0 references

isomeric SMILES

COC(=O)[C@@H](Cc1ccc(O)c(O)c1)OC(=O)/C=C/c1ccc(O)c(O)c1

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found in taxon

Isodon coetsa

1 reference

Three angiotensin-converting enzyme inhibitors from Rabdosia coetsa

Salvia bowleyana

1 reference

Salvia miltiorrhiza

2 references

Isolation of inhibitors of adenylate cyclase from dan-shen, the root of Salvia miltiorrhiza

Salvia prionitis

2 references

Prionitisides A and B, two phenolic glycosides from Salvia prionitis

Salvia sonchifolia

1 reference

Glechoma hederacea

2 references

Anti-inflammatory activity of constituents from Glechoma hederacea var. longituba

Anti-inflammatory activity of constituents from Glechoma hederacea var. longituba

Bourreria pulchra

1 reference

Benzochromenes from the roots of Bourreria pulchra

Cordia sebestena

1 reference

Sebestenoids A-D, BACE1 inhibitors from Cordia sebestena

Melissa officinalis

1 reference

A New Antioxidative 1,3-Benzodioxole fromMelissa officinalis

Origanum dictamnus

1 reference

Depsides and other polar constituents from Origanum dictamnus L. and their in vitro antimicrobial activity in clinical strains.

Dimetia scandens

1 reference

Five new phenolic glycosides from Hedyotis scandens

Lindelofia stylosa

1 reference

Phenyl polypropanoids from Lindelofia stylosa.

Rosmarinus officinalis

1 reference

Phytochemical Profiling of Flavonoids, Phenolic Acids, Terpenoids, and Volatile Fraction of a Rosemary (Rosmarinus officinalis L.) Extract.

Agastache rugosa

1 reference

Chemical Constituents from the Aerial Parts of Agastache rugosa and Their Inhibitory Activities on Prostaglandin E2 Production in Lipopolysaccharide-Treated RAW 264.7 Macrophages

Sarcandra glabra

1 reference

Chemical profiling of bioactive constituents in Sarcandra glabra and its preparations using ultra‐high‐pressure liquid chromatography coupled with LTQ Orbitrap mass spectrometry

Perilla frutescens

2 references

Identification and quantitation of phenolic compounds from the seed and pomace of Perilla frutescens using HPLC/PDA and HPLC-ESI/QTOF/MS/MS

Characterisation of phenolic phytochemicals and quality changes related to the harvest times from the leaves of Korean purple perilla (Perilla frutescens)

Salvia officinalis

1 reference

Comparison of Conventional and Ultrasound-assisted Extraction Techniques on Mass Fraction of Phenolic Compounds from Sage (Salvia officinalis L.)

Identifiers

InChI

InChI=1S/C19H18O8/c1-26-19(25)17(10-12-3-6-14(21)16(23)9-12)27-18(24)7-4-11-2-5-13(20)15(22)8-11/h2-9,17,20-23H,10H2,1H3/b7-4+/t17-/m1/s1

0 references

0 references

CAS Registry Number

99353-00-1

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

2 references

26 December 2021

ChEBI ID

175804

mapping relation type

exact match

2 references

ChEBI release 2022-06-13

International Chemical Identifier

InChI

InChI=1S/C19H18O8/c1-26-19(25)17(10-12-3-6-14(21)16(23)9-12)27-18(24)7-4-11-2-5-13(20)15(22)8-11/h2-9,17,20-23H,10H2,1H3/b7-4+/t17-/m1/s1

1 reference

1 reference

Human Metabolome Database ID

HMDB0035446

2 references

inferred from InChIKey