(Q72443757)

inferred from SMILES

265.07389321200003 dalton

1 reference

inferred from InChI

chemical formula

C₁₈H₁₁NO₃

2 references

The constituents and their bioactivities of Houttuynia cordata

20 April 2023

20 April 2023

COC1=C(C2=C3C(=C1)C(=O)NC3=CC4=CC=CC=C42)O

1 reference

20 April 2023

4 references

Aristolactams and a 4,5-dioxoaporphine derivative from Houttuynia cordata

Simultaneous quantification of eight bioactive components of Houttuynia cordata and related Saururaceae medicinal plants by on-line high performance liquid chromatography-diode array detector-electrospray mass spectrometry.

Anti-complementary constituents of Houttuynia cordata and their targets in complement activation cascade

Piper sanctum

5 references

Antifungal Compounds from Piper Species

Lignans, an amide and anti-platelet activities from Piper philippinum

Aristolochia heterophylla

3 references

The constituents of the root and stem of Aristolochia heterophylla Hemsl

The Constituents of the Leaves of Aristolochia heterophylla HEMSL.

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Fissistigma balansae

2 references

Aristolactams and dioxoaporphines from Fissistigma balansae and Fissistigma oldhamii

Aristolactams and dioxoaporphines from Fissistigma balansae and Fissistigma oldhamii

Piper philippinum

3 references

Lignans, an amide and anti-platelet activities from Piper philippinum

Lignans, an amide and anti-platelet activities from Piper philippinum

Aristolochia cucurbitifolia

1 reference

The constituents of the root and stem of Aristolochia cucurbitifolia Hayata and their biological activity

Piper argyrophyllum

1 reference

Neolignans and alkaloids from Piper argyrophylum

Piper longum

5 references

Aristolactams and 4,5-dioxoaporphines from Piper longum

Aristolactams and 4,5-dioxoaporphines from Piper longum

Lignans, an amide and anti-platelet activities from Piper philippinum

Aristolactams and dioxoaporphines from Fissistigma balansae and Fissistigma oldhamii

20 April 2023

4 references

Discovery and synthesis of new immunosuppressive alkaloids from the stem of Fissistigma oldhamii (Hemsl.) Merr

Discovery and synthesis of new immunosuppressive alkaloids from the stem of Fissistigma oldhamii (Hemsl.) Merr

538

retrieved

20 April 2023

Fissistigma bracteolatum

1 reference

Potential Anti-Inflammatory Activities of Bractelactone and other Compounds Isolated fromFissistigma bracteolatum

Goniothalamus tapis

1 reference

Chemical studies on Goniothalamus tapis Miq.

Piper attenuatum

3 references

Aristolactams and 4,5-dioxoaporphines from Piper longum

Lignans, an amide and anti-platelet activities from Piper philippinum

Piper hamiltonii

1 reference

Aristolactams and 4,5-dioxoaporphines from Piper longum

Piper kadsura

1 reference

The chemical constituents of Piper kadsura and their cytotoxic and anti-neuroinflammtaory activities

Piper kwashoense

1 reference

Lignans, an amide and anti-platelet activities from Piper philippinum

Piper lolot

1 reference

Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot.

Piper sarmentosum

1 reference

Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot.

Piper taiwanense

1 reference

Aristolactams and 4,5-dioxoaporphines from Piper longum

Fissistigma retusum

1 reference

Potential Anti-Inflammatory Activities of Bractelactone and other Compounds Isolated fromFissistigma bracteolatum

Fissistigma glaucescens

2 references

Alkaloids from the Leaves ofFissistigma Glaucescens

538

retrieved

20 April 2023

Aristolochia kaempferi

3 references

The Constituents of the Leaves of Aristolochia heterophylla HEMSL.

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Constituents from the stem and root of Aristolochia kaempferi

Piper auritum

3 references

Lignans, an amide and anti-platelet activities from Piper philippinum

Antifungal Compounds from Piper Species

InChI=1S/C16H11NO3/c1-20-12-7-10-13-11(17-16(10)19)6-8-4-2-3-5-9(8)14(13)15(12)18/h2-7,18H,1H3,(H,17,19)

Identifiers

InChI

0 references

InChIKey

KBGNBPGXVKPRQI-UHFFFAOYSA-N

0 references

CAS Registry Number

112501-42-5

1 reference

InChIKey

KBGNBPGXVKPRQI-UHFFFAOYSA-N

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=112501-42-5

0 references

mapping relation type

exact match

1 reference

DSSTOX compound identifier

ChEBI release 2022-06-13

1 reference

0 references

DTXCID4072574

0 references

Human Metabolome Database ID

HMDB0033060

1 reference

inferred from InChIKey

KNApSAcK ID

C00027470

1 reference

Google Knowledge Graph ID

inferred from InChIKey

/g/11qnvml5lz

0 references

Nikkaji ID

J790.693E

0 references