(Q15410885)

Chaetoglobosin A (English)

21 September 2016

chemical formula

C₃₂H₃₆N₂O₅

1 reference

Chaetoglobosin A (English)

21 September 2016

canonical SMILES

CC1CC=CC2C3C(O3)(C(C4C2(C(=O)C=CC(=O)C(C(=C1)C)O)C(=O)NC4CC5=CNC6=CC=CC=C65)C)C

1 reference

Chaetoglobosin A (English)

21 September 2016

isomeric SMILES

C[C@H]\1C/C=C/[C@H]2[C@H]3[C@](O3)([C@H]([C@@H]4[C@@]2(C(=O)/C=C/C(=O)[C@@H](/C(=C1)/C)O)C(=O)N[C@H]4CC5=CNC6=CC=CC=C65)C)C

1 reference

Chaetoglobosins Q, R, and T, three further new metabolites from Chaetomium globosum.

Chaetoglobosin A (English)

21 September 2016

6 references

Chaetoglobosins Q, R, and T, three further new metabolites from Chaetomium globosum.

Bioactive metabolites produced by Chaetomium globosum, an endophytic fungus isolated from Ginkgo biloba

Chaetoglobosins, cytotoxic 10-(indol-3-yl)-[13]cytochalasans from Chaetomium spp. I. Production, isolation and some cytological effects of chaetoglobosins A-J

Chaetoglobosins, cytotoxic 10-(indol-3-yl)-(13)cytochalasans from Chaetomium spp. IV. 13C-Nuclear magnetic resonance spectra and their application to a biosynthetic study.

Biosynthesis of the Cytochalasans. Biosynthetic studies on chaetoglobosin A and 19-O-acetylchaetoglobosin A

Calonectria kyotensis

1 reference

Chaetoglobosin O and Other Phytotoxic Metabolites from Cylindrocladium floridanum, a Causal Fungus of Alfalfa Black Rot Disease.

Penicillium

1 reference

Penochalasins, a novel class of cytotoxic cytochalasans from a Penicillium species separated from a marine alga: structure determination and solution conformation

Chaetomium

2 references

Isolation and characterization of bioactive metabolites from marine-derived filamentous fungi collected from tropical and sub-tropical coral reefs

A screening method for antimitotic and antifungal substances using conidia of Pyricularia oryzae, modification and application to tropical marine fungi

Chaetomium subaffine

2 references

Useful approach to find the plausible biosynthetic precursors of secondary metabolites using P-450 inhibitors: postulated intermediates of chaetoglobosin A

Biosynthetic study of chaetoglobosin A: origins of the oxygen and hydrogen atoms, and indirect evidence for biological Diels–Alder reaction

Penicillium aurantiogriseum

1 reference

Penicillium aurantiogriseum Dierckx produces chaetoglobosin A toxic to embryonic chickens

Identifiers

InChI

InChI=1S/C32H36N2O5/c1-17-8-7-10-22-29-31(4,39-29)19(3)27-24(15-20-16-33-23-11-6-5-9-21(20)23)34-30(38)32(22,27)26(36)13-12-25(35)28(37)18(2)14-17/h5-7,9-14,16-17,19,22,24,27-29,33,37H,8,15H2,1-4H3,(H,34,38)/b10-7+,13-12+,18-14+/t17-,19-,22-,24-,27-,28+,29-,31+,32+/m0/s1

1 reference

Chaetoglobosin A (English)

OUMWCYMRLMEZJH-VOXRAUTJSA-N

21 September 2016

InChIKey

1 reference

OUMWCYMRLMEZJH-VOXRAUTJSA-N

Chaetoglobosin A (English)

21 September 2016

1 reference

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=50335-03-0

1 reference

(13)Cytochalasa-13,17,21-triene-1,20,23-trione, 6,7-epoxy-19-hydroxy-10-(1H-indol-3-yl)-16,18-dimethyl-, (7S,13E,16S,17E,19R,21E)- (English)

21 September 2016

1 reference

Chaetoglobosin A (English)

21 September 2016

ChEBI ID

68798

mapping relation type

exact match

1 reference

ChEBI release 2022-06-13

1 reference

splash10-001i-0911000000-96aac4e9016ab9304d0f

CHAETOGLOBOSIN A (English)

21 September 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

splash10-001i-0942010000-2952d30236af81993a56

0 references

DSSTox substance ID

DTXSID20891790

0 references

DSSTOX compound identifier

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download