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GO:1900778 fumiquinazoline A biosynthetic process

Term Information

ID GO:1900778
Name fumiquinazoline A biosynthetic process
Ontology Biological Process
Definition The chemical reactions and pathways resulting in the formation of fumiquinazoline A.
GONUTS GO:1900778 Wiki Page

Synonyms

Synonyms are alternative words or phrases closely related in meaning to the term name, with indication of the relationship between the name and synonym given by the synonym scope. Click on the icon for more details.
Type Synonym
exact fumiquinazoline A biosynthesis
exact fumiquinazoline A synthesis
exact fumiquinazoline A formation
exact fumiquinazoline A anabolism

Cross-Ontology Relations

Relation Other Ontology ID Term
has_output CHEBI CHEBI:64546 fumiquinazoline A

Ancestor Chart

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Child Terms

This table lists all terms that are direct descendants (child terms) of GO:1900778:
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Protein Annotation

Displaying annotations FIRST to LAST of TOTAL Page size: Additional filters: Bookmarkable link
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Co-occurring Terms

These tables show the number of times the term listed in the table has been co-annotated with GO:1900778. The terms are listed in descending order of number of times the term has been co-annotated.
The table on the left is calculated using both electronic and manual-evidenced annotations, while the table on the right is calculated using only manual-evidenced annotations.
Co-occurrence statistics for GO:1900778 based on the entire annotation set Co-occurrence statistics for GO:1900778 based on non-IEA annotations only

Change Log

All changes

Timestamp Action Category Detail
2012-10-29 Deleted RELATION is a GO:0035835 (indole alkaloid biosynthetic process)
2012-10-29 Deleted RELATION is a GO:0018130 (heterocycle biosynthetic process)
2012-10-19 Added RELATION is a GO:1900775 (fumiquinazoline biosynthetic process)
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 biosynthetic process
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 formation
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 synthesis
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 biosynthesis
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 biosynthesis
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione formation
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N biosynthetic process
2012-06-12 Deleted SYNONYM C24H23N5O4 anabolism
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione biosynthesis
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione biosynthetic process
2012-06-12 Deleted SYNONYM C24H23N5O4 synthesis
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione anabolism
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione synthesis
2012-06-12 Deleted SYNONYM C24H23N5O4 formation
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 synthesis
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 biosynthetic process
2012-06-12 Deleted SYNONYM C24H23N5O4 biosynthesis
2012-06-12 Deleted SYNONYM C24H23N5O4 biosynthetic process
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N biosynthesis
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 anabolism
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N formation
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N anabolism
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 formation
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N synthesis
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 anabolism
2012-06-07 Added TERM fumiquinazoline A biosynthetic process
2012-06-07 Added DEFINITION The chemical reactions and pathways resulting in the formation of fumiquinazoline A.
2012-06-07 Added SYNONYM C24H23N5O4 biosynthesis
2012-06-07 Added SYNONYM fumiquinazoline A biosynthesis
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione synthesis
2012-06-07 Added SYNONYM C24H23N5O4 formation
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 anabolism
2012-06-07 Added SYNONYM C24H23N5O4 synthesis
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N anabolism
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N formation
2012-06-07 Added SYNONYM fumiquinazoline A formation
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 biosynthesis
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 synthesis
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N biosynthetic process
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N synthesis
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 biosynthetic process
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N biosynthesis
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 biosynthetic process
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 formation
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 synthesis
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 anabolism
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 formation
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 biosynthesis
2012-06-07 Added SYNONYM fumiquinazoline A anabolism
2012-06-07 Added SYNONYM fumiquinazoline A synthesis
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione anabolism
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione biosynthesis
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione biosynthetic process
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione formation
2012-06-07 Added SYNONYM C24H23N5O4 anabolism
2012-06-07 Added SYNONYM C24H23N5O4 biosynthetic process
2012-06-07 Added RELATION is a GO:1900776 (fumiquinazoline A metabolic process)
2012-06-07 Added RELATION is a GO:0035835 (indole alkaloid biosynthetic process)
2012-06-07 Added RELATION is a GO:0018130 (heterocycle biosynthetic process)

Term

Timestamp Action Category Detail
2012-06-07 Added TERM fumiquinazoline A biosynthetic process

Definition/synonyms

Timestamp Action Category Detail
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 biosynthetic process
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 formation
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 synthesis
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 biosynthesis
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 biosynthesis
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione formation
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N biosynthetic process
2012-06-12 Deleted SYNONYM C24H23N5O4 anabolism
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione biosynthesis
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione biosynthetic process
2012-06-12 Deleted SYNONYM C24H23N5O4 synthesis
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione anabolism
2012-06-12 Deleted SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione synthesis
2012-06-12 Deleted SYNONYM C24H23N5O4 formation
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 synthesis
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 biosynthetic process
2012-06-12 Deleted SYNONYM C24H23N5O4 biosynthesis
2012-06-12 Deleted SYNONYM C24H23N5O4 biosynthetic process
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N biosynthesis
2012-06-12 Deleted SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 anabolism
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N formation
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N anabolism
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 formation
2012-06-12 Deleted SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N synthesis
2012-06-12 Deleted SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 anabolism
2012-06-07 Added DEFINITION The chemical reactions and pathways resulting in the formation of fumiquinazoline A.
2012-06-07 Added SYNONYM C24H23N5O4 biosynthesis
2012-06-07 Added SYNONYM fumiquinazoline A biosynthesis
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione synthesis
2012-06-07 Added SYNONYM C24H23N5O4 formation
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 anabolism
2012-06-07 Added SYNONYM C24H23N5O4 synthesis
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N anabolism
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N formation
2012-06-07 Added SYNONYM fumiquinazoline A formation
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 biosynthesis
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 synthesis
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N biosynthetic process
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N synthesis
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 biosynthetic process
2012-06-07 Added SYNONYM InChIKey=DQQCCKFZJNINST-VCPZKGNQSA-N biosynthesis
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 biosynthetic process
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 formation
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 synthesis
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 anabolism
2012-06-07 Added SYNONYM InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1 formation
2012-06-07 Added SYNONYM [H][C@]12N[C@@H](C)C(=O)N1c1ccccc1[C@@]2(O)C[C@@H]1C(=O)N[C@@H](C)c2nc3ccccc3c(=O)n12 biosynthesis
2012-06-07 Added SYNONYM fumiquinazoline A anabolism
2012-06-07 Added SYNONYM fumiquinazoline A synthesis
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione anabolism
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione biosynthesis
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione biosynthetic process
2012-06-07 Added SYNONYM (1S,4R)-4-{[(2S,9S,9aS)-9-hydroxy-2-methyl-3-oxo-2,3,9,9a-tetrahydro-1H-imidazo[1,2-a]indol-9-yl]methyl}-1-methyl-2H-pyrazino[2,1-b]quinazoline-3,6(1H,4H)-dione formation
2012-06-07 Added SYNONYM C24H23N5O4 anabolism
2012-06-07 Added SYNONYM C24H23N5O4 biosynthetic process

Relationships

Timestamp Action Category Detail
2012-10-29 Deleted RELATION is a GO:0035835 (indole alkaloid biosynthetic process)
2012-10-29 Deleted RELATION is a GO:0018130 (heterocycle biosynthetic process)
2012-10-19 Added RELATION is a GO:1900775 (fumiquinazoline biosynthetic process)
2012-06-07 Added RELATION is a GO:1900776 (fumiquinazoline A metabolic process)
2012-06-07 Added RELATION is a GO:0035835 (indole alkaloid biosynthetic process)
2012-06-07 Added RELATION is a GO:0018130 (heterocycle biosynthetic process)
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