(Q43513516)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Atranones A-G, from the toxigenic mold Stachybotrys chartarum (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

[(1S,4Z,9S,10S,11Z,14R)-9-hydroxy-1,4,11-trimethyl-7,17-dioxo-15-propan-2-yl-6,18-dioxatricyclo[12.4.0.05,9]octadeca-4,11,15-trien-10-yl] acetate

3 November 2019

main subject

Stachybotrys chartarum

2 references

1 reference

1 reference

1 reference

(1S,4E,8R,9R,10E,14R)-8-[(1S)-1-hydroxyethyl]-1,4,11-trimethyl-15-propan-2-yl-6-oxatricyclo[12.3.0.05,9]heptadeca-4,10,15-triene-7,17-dione

1 reference

(3aS,5E,8R,9E,12aR)-8-hydroxy-3a,6,10-trimethyl-1-propan-2-yl-4,7,8,11,12,12a-hexahydrocyclopenta[11]annulen-3-one

1 reference

(1S,4E,8S,9R,11R,12Z)-1,4,9,12-Tetramethyl-5,8,11-[(R)-methanetriyl]-9-hydroxy-16-isopropyl-6,10,19-trioxabicyclo[13.4.0]nonadecane-4,12,15-triene-7,18-dione

1 reference

[(1S,4E,9S,10R,11Z,14R)-9-hydroxy-16-methoxy-1,4,11-trimethyl-7,17-dioxo-15-propan-2-yl-6,18-dioxatricyclo[12.4.0.05,9]octadeca-4,11,15-trien-10-yl] acetate

1 reference

(1E,5R,10S,12Z,14R,16S,17R,20S)-16-hydroxy-8-methoxy-2,5,13,16-tetramethyl-9-propan-2-yl-6,15,19-trioxatetracyclo[12.5.1.05,10.017,20]icosa-1,8,12-triene-7,18-dione

1 reference

(1E,5S,10R,12E,14R,16R,17S,20R)-16-hydroxy-2,5,13,16-tetramethyl-9-propan-2-yl-6,15,19-trioxatetracyclo[12.5.1.05,10.017,20]icosa-1,8,12-triene-7,18-dione

1 reference

[(1S,4Z,9S,10S,11Z,14R)-9-hydroxy-16-methoxy-1,4,11-trimethyl-7,17-dioxo-15-propan-2-yl-6,18-dioxatricyclo[12.4.0.05,9]octadeca-4,11,15-trien-10-yl] acetate

1 reference

[(1R,4E,9S,10S,11Z,14R)-9-hydroxy-1,4,11-trimethyl-7,17-dioxo-15-propan-2-yl-6,18-dioxatricyclo[12.4.0.05,9]octadeca-4,11,15-trien-10-yl] acetate

1 reference

(1R,4E,8R,9S,10E,14R)-8-[(1S)-1-hydroxyethyl]-1,4,11-trimethyl-15-propan-2-yl-6-oxatricyclo[12.3.0.05,9]heptadeca-4,10,15-triene-7,17-dione

1 reference

(1Z,5S,12E,14R,16R,17S,20R)-16-hydroxy-2,5,13,16-tetramethyl-9-propan-2-yl-6,15,19-trioxatetracyclo[12.5.1.05,10.017,20]icosa-1,9,12-triene-7,18-dione

1 reference

(1Z,5S,12Z,14R,16R,17S,20R)-16-hydroxy-2,5,13,16-tetramethyl-9-propan-2-yl-6,15,19-trioxatetracyclo[12.5.1.05,10.017,20]icosa-1,9,12-triene-7,18-dione

1 reference

(1S*,3R*,4R*,6S*,11S*)-3,4-epoxy-6-hydroxydolabella-7E,12-dien-14-one

1 reference

(1S*,6S*,11S*)-6alpha-Hydroxydolabella-3E,7E,12-trien-14-one

1 reference

(1Z,5S,10R,12E,14R,16R,17S,20R)-16-hydroxy-2,5,13,16-tetramethyl-9-propan-2-yl-6,15,19-trioxatetracyclo[12.5.1.05,10.017,20]icosa-1,8,12-triene-7,18-dione

1 reference

[(1S,4E,9S,10R,11Z,14R)-9-hydroxy-1,4,11-trimethyl-7,17-dioxo-15-propan-2-yl-6,18-dioxatricyclo[12.4.0.05,9]octadeca-4,11,15-trien-10-yl] acetate

1 reference

(1E,5S,10R,12Z,14S,16R,17S,20R)-16-hydroxy-2,5,13,16-tetramethyl-9-propan-2-yl-6,15,19-trioxatetracyclo[12.5.1.05,10.017,20]icosa-1,8,12-triene-7,18-dione

1 reference

1 reference

1 reference

(1S,4Z,8S,9R,10E,14R)-8-[(1S)-1-hydroxyethyl]-1,4,11-trimethyl-15-propan-2-yl-6-oxatricyclo[12.3.0.05,9]heptadeca-4,10,15-triene-7,17-dione

1 reference

1 reference

(1E,5S,10R,12E,14R,16R,17S,20R)-16-hydroxy-8-methoxy-2,5,13,16-tetramethyl-9-propan-2-yl-6,15,19-trioxatetracyclo[12.5.1.05,10.017,20]icosa-1,8,12-triene-7,18-dione

1 reference

1 reference

1 reference

(1E,5S,10R,12Z,14S,16R,17S,20R)-16-hydroxy-8-methoxy-2,5,13,16-tetramethyl-9-propan-2-yl-6,15,19-trioxatetracyclo[12.5.1.05,10.017,20]icosa-1,8,12-triene-7,18-dione

1 reference

(1S,3R,5R,7S,8E,12R)-7-hydroxy-1,5,9-trimethyl-13-propan-2-yl-4-oxatricyclo[10.3.0.03,5]pentadeca-8,13-dien-15-one

1 reference

1 reference

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

James C Fettinger

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

author name string

E P Mazzola

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Y F Lam

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

B B Jarvis

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

publication date

November 2000

3 references

16 September 2022

16 September 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

55

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

page(s)

663-673

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

An empirical correction for absorption anisotropy.

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Overview of investigations into pulmonary hemorrhage among infants in Cleveland, Ohio

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Acute pulmonary hemorrhage in infants associated with exposure to Stachybotrys atra and other fungi.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Further neolignans from Ocotea aciphylla

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Striatin A, B, and C: novel diterpenoid antibiotics from Cyathus striatus; X-ray crystal structure of striatin A

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Atranones: Novel diterpenoids from the toxigenic mold Stachybotrys atra

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Trichothecenes produced by Stachybotrys atra from Eastern Europe

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Stachybotrys toxins. 1

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Study of toxin production by isolates of Stachybotrys chartarum and Memnoniella echinata isolated during a study of pulmonary hemosiderosis in infants

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Erinacines E, F, and G, stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Antitumour plants. Part 6. Novel modified germacranolides and other constituents of Eremanthus elaeagnus Schultz-bip (compositae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Antitumor plants. 12. Further sesquiterpenoid constituents of Lychnophora affinis Gardn. (Compositae). X-ray structure analysis of lychnophorolide A

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Enzymology and Molecular Biology of Aflatoxin Biosynthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Phthalide Dimers from Ligusticum chuangxiong Hort.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Eremantholide A, a novel tumor-inhibiting compound from Eremanthus elaeagnus (Compositae)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Erinacine E as a kappa opioid receptor agonist and its new analogs from a basidiomycete, Hericium ramosum

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Phase annealing in SHELX-90: direct methods for larger structures

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

Structures and reactivities of new dolabellane diterpenoids from the Caribbean gorgonian Eunicea laciniata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2800%2900231-4

7 January 2021

10.1016/S0031-9422(00)00231-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11130678%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference