(Q43959386)

inferred from SMILES

chemical structure

Parviflorin.svg
558 × 366; 58 KB

0 references

mass

594.449554324 dalton

1 reference

inferred from isomeric SMILES

stereoisomer of

(2S)-4-[(2R,11R)-2,11-dihydroxy-11-[(2S,5S)-5-[(2S,5S)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

2 references

(2R)-4-[(2S,11R)-2,11-dihydroxy-11-[(2R,5R)-5-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

2 references

(2S)-4-[(2R,11S)-2,11-dihydroxy-11-[(2S,5S)-5-[(2S,5S)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

2 references

2 references

(2R)-4-[(2R,11R)-2,11-dihydroxy-11-[(2R,5R)-5-[(2R,5R)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

2 references

3-{2,11-Dihydroxy-11-[5''-(1-hydroxy-undecyl)-octahydro-[2,2'']bifuranyl-5-yl]-undecyl}-5-methyl-5H-furan-2-one(Rollimembrin)

1 reference

1 reference

(2R)-4-[(2S,11S)-2,11-dihydroxy-11-[(2S,5S)-5-[(2S,5S)-5-[(1R)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

1 reference

(R)-3-[(2R,11R)-11-[[(2R,2'R,5R,5'R)-5'-[(R)-1-Hydroxyundecyl]octahydro-2,2'-bifuran]-5-yl]-2,11-dihydroxyundecyl]-5beta-methylfuran-2(5H)-one

1 reference

(2R)-4-[(2S,11R)-2,11-dihydroxy-11-[(2R,5S)-5-[(2R,5S)-5-[(1S)-1-hydroxyundecyl]oxolan-2-yl]oxolan-2-yl]undecyl]-2-methyl-2H-furan-5-one

1 reference

1 reference

C₃₅H₆₂O₇

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canonical SMILES

CCCCCCCCCCC(C1CCC(O1)C2CCC(O2)C(CCCCCCCCC(CC3=CC(OC3=O)C)O)O)O

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isomeric SMILES

CCCCCCCCCC[C@H]([C@H]1CC[C@@H](O1)[C@H]2CC[C@@H](O2)[C@@H](CCCCCCCC[C@H](CC3=C[C@@H](OC3=O)C)O)O)O

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found in taxon

Annona squamosa

2 references

Natural acetogenins from annonaceae, synthesis and mechanisms of action

Annonaceous Acetogenins from the Seeds of Annona squamosa. Adjacent Bis-tetrahydrofuranic Acetogenins.

Vanda parviflora

1 reference

Parviflorin a phenanthropyran from Vanda parviflora

Vanda testacea

1 reference

Parviflorin a phenanthropyran from Vanda parviflora

Annona bullata

1 reference

Bullacin: A New Cytotoxic Annonaceous Acetogenin from Annona bullata

Annona glabra

1 reference

Acetogenins from Annona glabra seeds

Annona glauca

1 reference

Leishmanicidal and Trypanocidal activities of Acetogenins isolated fromAnnona glauca

Asimina parviflora

1 reference

Parvifloracin and parviflorin: cytotoxic bistetrahydrofuran acetogenins with 35 carbons from Asimina parviflora (Annonaceae)

described by source

Parvifloracin and parviflorin: cytotoxic bistetrahydrofuran acetogenins with 35 carbons from Asimina parviflora (Annonaceae)

0 references

Identifiers

InChI

InChI=1S/C35H62O7/c1-3-4-5-6-7-8-12-15-18-29(37)31-20-22-33(41-31)34-23-21-32(42-34)30(38)19-16-13-10-9-11-14-17-28(36)25-27-24-26(2)40-35(27)39/h24,26,28-34,36-38H,3-23,25H2,1-2H3/t26-,28+,29+,30+,31+,32+,33+,34+/m0/s1

0 references

InChIKey

YVZIPERWMPDEIZ-GHRGOOLJSA-N

0 references

2 references

28 November 2017

YVZIPERWMPDEIZ-GHRGOOLJSA-N

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=152378-19-3

0 references

1 reference

matched by identifier from

InChIKey

YVZIPERWMPDEIZ-GHRGOOLJSA-N

ChEBI ID

176190

mapping relation type

exact match

2 references

matched by identifier from

ChEBI release 2022-06-13

International Chemical Identifier

InChI

InChI=1S/C35H62O7/c1-3-4-5-6-7-8-12-15-18-29(37)31-20-22-33(41-31)34-23-21-32(42-34)30(38)19-16-13-10-9-11-14-17-28(36)25-27-24-26(2)40-35(27)39/h24,26,28-34,36-38H,3-23,25H2,1-2H3/t26-,28+,29+,30+,31+,32+,33+,34+/m0/s1

0 references

1 reference

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1 reference

inferred by common MeSH mappings on source and on Wikidata