(Q10853851)

(2R)-2-hydroxy-3-[(2R,6R)-6-hydroxy-5-[4-methyl-6-(2,6,6-trimethylcyclohexen-1-yl)hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl]-2H-furan-5-one

manoalide (English)

7 October 2016

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(2S)-2-hydroxy-3-[(2R,6R)-6-hydroxy-5-[(E)-4-methyl-6-(2,6,6-trimethylcyclohexen-1-yl)hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl]-2H-furan-5-one

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₅H₃₆O₅

1 reference

manoalide (English)

7 October 2016

CC1=C(C(CCC1)(C)C)CCC(=CCCC2=CCC(OC2O)C3=CC(=O)OC3O)C

1 reference

manoalide (English)

7 October 2016

CC1=C(C(CCC1)(C)C)CC/C(=C/CCC2=CC[C@@H](O[C@H]2O)C3=CC(=O)O[C@H]3O)/C

1 reference

Four New Antibacterial Sesterterpenes from a Marine Sponge of the Genus Luffariella

manoalide (English)

7 October 2016

2 references

Luffasterols A-C, 9,11-secosterols from the Palauan sponge Luffariella sp.

Luffariella variabilis

3 references

Acetylated Sesterterpenes from the Great Barrier Reef SpongeLuffariella variabilis§

Manoalide, an antibiotic sesterterpenoid from the marine sponge (polejaeff)

1 reference

Fasciospongides A, B, and C, New Manoalide Derivatives from the Sponge Fasciospongia sp.

Hyrtios erectus

1 reference

Marine natural products. XXXII. Absolute configurations of C-4 of the manoalide family, biologically active sesterterpenes from the marine sponge Hyrtios erecta

Fasciospongia cavernosa

1 reference

A new cacospongionolide inhibitor of human secretory phospholipase A2 from the Tyrrhenian sponge Fasciospongia cavernosa and absolute configuration of cacospongionolides

Spongiidae

3 references

Four New Antibacterial Sesterterpenes from a Marine Sponge of the Genus Luffariella

Fasciospongides A, B, and C, New Manoalide Derivatives from the Sponge Fasciospongia sp.

Luffasterols A-C, 9,11-secosterols from the Palauan sponge Luffariella sp.

subject has role

non-steroidal anti-inflammatory drug

1 reference

15 March 2018

1 reference

15 March 2018

calcium channel blocker

1 reference

phosphodiesterase inhibitors

15 March 2018

1 reference

InChI=1S/C25H36O5/c1-16(10-12-20-17(2)8-6-14-25(20,3)4)7-5-9-18-11-13-21(29-23(18)27)19-15-22(26)30-24(19)28/h7,11,15,21,23-24,27-28H,5-6,8-10,12-14H2,1-4H3/b16-7+/t21-,23-,24-/m1/s1

15 March 2018

Identifiers

InChI

1 reference

manoalide (English)

7 October 2016

2 references

manoalide (English)

7 October 2016

ChEBI release 2020-09-01

2 references

manoalide (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=75088-80-1

8 April 2021

1 reference

Manoalide (English)

7 October 2016

2 references

English

title

manoalide (English)

7 October 2016

InChIKey

Reaxys registry number

10729444

1 reference

manoalide (English)

7 October 2016

mapping relation type

2 references

English

title

manoalide (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C25H36O5/c1-16(10-12-20-17(2)8-6-14-25(20,3)4)7-5-9-18-11-13-21(29-23(18)27)19-15-22(26)30-24(19)28/h7,11,15,21,23-24,27-28H,5-6,8-10,12-14H2,1-4H3/b16-7+/t21-,23-,24-/m1/s1

1 reference

MANOALIDE (English)

7 October 2016

1 reference

1 reference

InChIKey

1 reference

Global Substance Registration System

14 March 2018

2 references

UNII

E1DK0157K9

English

title

MANOALIDE (English)

7 October 2016

InChIKey

0 references

1 reference

inferred by common MeSH mappings on source and on Wikidata

manoalide (English)

7 October 2016

0 references

0 references

Microsoft Academic ID

0 references

1 reference

UMLS 2023