(Q27134531)

CHEBI:66028 (English)

5-Hydroxy-2-[(R)-1-hydroxyethyl]naphtho[2,3-b]furan-4,9-dione

7 October 2016

stereoisomer of

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₄H₁₀O₅

1 reference

CHEBI:66028 (English)

7 October 2016

canonical SMILES

CC(C1=CC2=C(O1)C(=O)C3=C(C2=O)C(=CC=C3)O)O

1 reference

CHEBI:66028 (English)

7 October 2016

isomeric SMILES

C[C@@H](C1=CC2=C(O1)C(=O)C3=C(C2=O)C(=CC=C3)O)O

1 reference

CHEBI:66028 (English)

Handroanthus impetiginosum

7 October 2016

found in taxon

6 references

Stereoselective synthesis and cytotoxicity of a cancer chemopreventive naphthoquinone from Tabebuia avellanedae

Synthesis and evaluation of bioactive naphthoquinones from the Brazilian medicinal plant, Tabebuia avellanedae

Studies on the structure and stereochemistry of cytotoxic furanonaphthoquinones from Tabebuia impetiginosa: 5- and 8-hydroxy-2-(1-hydroxyethyl)naphtho[2,3-b]furan-4,9-diones

Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique

Production of anti-tumour-promoting furanonaphthoquinones in Tabebuia avellanedae cell cultures

Micellar electrokinetic chromatography (MEKC) separation of furanonaphthoquinones from Tabebuia impetiginosa

Handroanthus incanus

1 reference

Bioactive dihydroxyfuranonaphthoquinones from the bark of Tabebuia incana A.H. Gentry (Bignoniaceae) and HPLC analysis of commercial pau d'arco and certified T.incana bark infusions

Tabebuia ochracea

1 reference

Chemical Investigation and in vitro Antimalarial Activity of Tabebuia ochracea ssp. neochrysantha

Handroanthus impetiginosus

6 references

Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique

Synthesis and evaluation of bioactive naphthoquinones from the Brazilian medicinal plant, Tabebuia avellanedae

Production of anti-tumour-promoting furanonaphthoquinones in Tabebuia avellanedae cell cultures

Micellar electrokinetic chromatography (MEKC) separation of furanonaphthoquinones from Tabebuia impetiginosa

Stereoselective synthesis and cytotoxicity of a cancer chemopreventive naphthoquinone from Tabebuia avellanedae

Studies on the structure and stereochemistry of cytotoxic furanonaphthoquinones from Tabebuia impetiginosa: 5- and 8-hydroxy-2-(1-hydroxyethyl)naphtho[2,3-b]furan-4,9-diones

Identifiers

InChI

InChI=1S/C14H10O5/c1-6(15)10-5-8-12(17)11-7(3-2-4-9(11)16)13(18)14(8)19-10/h2-6,15-16H,1H3/t6-/m0/s1

1 reference

CHEBI:66028 (English)

XJGFVZBTNKODFQ-LURJTMIESA-N

7 October 2016

InChIKey

2 references

CHEBI:66028 (English)

7 October 2016

ChEBI release 2020-09-01

2 references

5-hydroxy-2-(1'-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione (English)

XJGFVZBTNKODFQ-LURJTMIESA-N

7 October 2016

InChIKey

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=123297-90-5

1 reference

5-Hydroxy-2-[(1S)-1-hydroxyethyl]naphtho[2,3-b]furan-4,9-dione (English)

7 October 2016

2 references

CHEBI:66028 (English)

matched by identifier from

7 October 2016

InChIKey

XJGFVZBTNKODFQ-LURJTMIESA-N

Reaxys registry number

5381025

1 reference

5-hydroxy-2-(1'-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione (English)

7 October 2016

ChEBI ID

66028

mapping relation type

2 references

5-hydroxy-2-(1'-hydroxyethyl)naphtho[2,3-b]furan-4,9-dione (English)

matched by identifier from

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C14H10O5/c1-6(15)10-5-8-12(17)11-7(3-2-4-9(11)16)13(18)14(8)19-10/h2-6,15-16H,1H3/t6-/m0/s1

1 reference