rosmanol (Q27277536)

inferred from SMILES

chemical structure

Rosmanol.svg
512 × 404; 22 KB

0 references

mass

346.178±0 dalton

1 reference

(1R,8S,9S,10R)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one

Rosmanol (English)

14 October 2016

2 references

inferred from InChIKey

(1R,8R,9S,10S)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one

inferred from InChI

1 reference

(1R,8R,9S,10R)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one

inferred from InChIKey

1 reference

inferred from InChI

chemical formula

C₂₀H₂₆O₅

1 reference

Rosmanol (English)

14 October 2016

CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O

1 reference

Rosmanol (English)

14 October 2016

CC(C)C1=C(C(=C2C(=C1)[C@@H]([C@@H]3[C@@H]4[C@@]2(CCCC4(C)C)C(=O)O3)O)O)O

1 reference

Abietane diterpenes with antibiotic activity from the flowers of Salviacanariensis. Reaction of galdosol with diazomethane

Rosmanol (English)

14 October 2016

5 references

Diterpenes from the flowers of Salvia canariensis

A revised structure for the diterpene rosmanol

Diterpenes from the roots of Salvia canariensis

Semisynthesis of rosmanol and its derivatives. Easy access to abietatriene diterpenes isolated from the genus Salvia with biological activities

Salvia mellifera

3 references

C-16 hydroxylated abietane diterpenes from Salvia Mellifera

Diterpenes from Salvia mellifera and their biogenetic significance

Diterpenes from Salvia mellifera

Salvia columbariae

1 reference

Diterpenes from the aerial part of Salvia columbariae

Salvia munzii

1 reference

Abietane diterpenes from Salvia munzii

Isodon grandifolius

1 reference

Terpenoids from Isodon grandifolia var. Atuntzensis

Salvia aurea

1 reference

Chemical composition of essential oils from some Salvia species

Lamiaceae

1 reference

Rosmanol potently inhibits lipopolysaccharide-induced iNOS and COX-2 expression through downregulating MAPK, NF-kappaB, STAT3 and C/EBP signaling pathways

Hypericum canariense

1 reference

Rosmanol controls explants browing of Hypericum canariensis L. during the in vitro estabilishment of shoots

Hyptis dilatata

1 reference

Tricyclic diterpenes from hyptys dilatata

Lepechinia urbanii

1 reference

Abietane diterpenes from Salvia napifolia

Salvia apiana

1 reference

Apiananes: C23 terpenoids with a new type of skeleton from Salvia apiana

Salvia officinalis

10 references

Apianane terpenoids from Salvia officinalis

A quinone methide from Salvia officinalis

Antioxidant Constituents in Sage (Salvia officinalis)

Structure activity relationship of phenolic diterpenes from Salvia officinalis as activators of the nuclear factor E2-related factor 2 pathway

Antioxidant Constituents in Sage (Salvia officinalis)

Apianane terpenoids from Salvia officinalis

A quinone methide from Salvia officinalis

Rearranged abietane-type diterpenes from Salvia dichroantha

Diterpenoid quinones from rosemary (Rosmarinus officinalis L.).

Antiprotozoal Diterpenes from Perovskia abrotanoides.

Salvia rubescens

1 reference

Abietane diterpenoids from Salvia rubescens ssp. truxillensis

Salvia tomentosa

2 references

Rearranged abietane-type diterpenes from Salvia dichroantha

Rearranged abietane-type diterpenes from Salvia dichroantha

Lepechinia salviae

1 reference

Antioxidant capacity of abietanes from Sphacele salviae

Salvia abrotanoides

1 reference

Cytotoxicity of abietane diterpenoids from Perovskia abrotanoides and of their semisynthetic analogues

Salvia

2 references

Diterpenoid quinones from rosemary (Rosmarinus officinalis L.).

Antiprotozoal Diterpenes from Perovskia abrotanoides.

Rosmarinus officinalis

8 references

High-performance liquid chromatographic determination of carnosic acid and carnosol in Rosmarinus officinalis and Salvia officinalis

Combined Use of Supercritical Fluid Extraction, Micellar Electrokinetic Chromatography, and Reverse Phase High Performance Liquid Chromatography for the Analysis of Antioxidants from Rosemary (RosmarinusofficinalisL.)

A New Diterpene Lactone, Rosmadial, from Rosemary (Rosmarinus officinalisL.)

Studies on medicinal plants in Paraguay; studies on "Romero"; Part 1

New Antimicrobial Substances againstStreptomyces scabiesfrom Rosemary (Rosmarinus officinalisL.)

Inhibitory effect of carnosic acid on HIV-1 protease in cell-free assays [corrected]

Inhibition of lipid peroxidation and superoxide generation by diterpenoids from Rosmarinus officinalis

Antioxidative constituents ofRosmarinus officinalis andSalvia officinalis

Lepechinia urbani

1 reference

Abietane diterpenes from Salvia napifolia

Identifiers

InChI

InChI=1S/C20H26O5/c1-9(2)10-8-11-12(15(23)13(10)21)20-7-5-6-19(3,4)17(20)16(14(11)22)25-18(20)24/h8-9,14,16-17,21-23H,5-7H2,1-4H3/t14-,16+,17-,20-/m0/s1

1 reference

LCAZOMIGFDQMNC-FORWCCJISA-N

Rosmanol (English)

14 October 2016

1 reference

Global Substance Registration System

Rosmanol (English)

14 October 2016

1 reference

UNII

F25TV383OC

rosmanol (English)

14 October 2016

1 reference

English

title

(6beta,7alpha)-7,11,12-Trihydroxy-6,20-epoxyabieta-8(14),9(11),12-trien-20-one (English)

14 October 2016

1 reference

Rosmanol (English)

14 October 2016

1 reference

matched by identifier from

ROSMANOL (English)

14 October 2016

2 references

inferred from InChIKey

InChIKey

LCAZOMIGFDQMNC-FORWCCJISA-N

1 reference

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

UNII

F25TV383OC