(Q27277644)

Nucleocidin (English)

14 October 2016

chemical formula

C₁₀H₁₃FN₆O₆S

1 reference

Nucleocidin (English)

14 October 2016

canonical SMILES

C1=NC2=C(C(=N1)N)N=CN2C3C(C(C(O3)(COS(=O)(=O)N)F)O)O

1 reference

Nucleocidin (English)

14 October 2016

isomeric SMILES

C1=NC2=C(C(=N1)N)N=CN2[C@H]3[C@@H]([C@@H]([C@](O3)(COS(=O)(=O)N)F)O)O

1 reference

Biosynthesis of the Fluorinated Natural Product Nucleocidin in Streptomyces calvus Is Dependent on the bldA-Specified Leu-tRNA(UUA) Molecule

Nucleocidin (English)

14 October 2016

7 references

The gene cluster for fluorometabolite biosynthesis in Streptomyces cattleya: a thioesterase confers resistance to fluoroacetyl-coenzyme A.

A cryptic polyene biosynthetic gene cluster in Streptomyces calvus is expressed upon complementation with a functional bldA gene

Natural occurrence of organofluorine and other constituents from Streptomyces sp. TC1.

Biosynthesis of the Fluorinated Natural Product Nucleocidin in Streptomyces calvus Is Dependent on the bldA-Specified Leu-tRNA(UUA) Molecule

Incorporation of [2H1]-(1R,2R)- and [2H1]-(1S,2R)-glycerols into the antibiotic nucleocidin in Streptomyces calvus.

Genome mining reveals the origin of a bald phenotype and a cryptic nucleocidin gene cluster in Streptomyces asterosporus DSM 41452

Streptomyces

1 reference

The structure of nucleocidin. 3. (A new structure)

Streptomyces asterosporus

6 references

Genome mining reveals the origin of a bald phenotype and a cryptic nucleocidin gene cluster in Streptomyces asterosporus DSM 41452

The gene cluster for fluorometabolite biosynthesis in Streptomyces cattleya: a thioesterase confers resistance to fluoroacetyl-coenzyme A.

A cryptic polyene biosynthetic gene cluster in Streptomyces calvus is expressed upon complementation with a functional bldA gene

Natural occurrence of organofluorine and other constituents from Streptomyces sp. TC1.

Biosynthesis of the Fluorinated Natural Product Nucleocidin in Streptomyces calvus Is Dependent on the bldA-Specified Leu-tRNA(UUA) Molecule

Incorporation of [2H1]-(1R,2R)- and [2H1]-(1S,2R)-glycerols into the antibiotic nucleocidin in Streptomyces calvus.

Commons category

Nucleocidin

0 references

Identifiers

InChI

InChI=1S/C10H13FN6O6S/c11-10(1-22-24(13,20)21)6(19)5(18)9(23-10)17-3-16-4-7(12)14-2-15-8(4)17/h2-3,5-6,9,18-19H,1H2,(H2,12,14,15)(H2,13,20,21)/t5-,6+,9-,10-/m1/s1

1 reference

Nucleocidin (English)

14 October 2016

1 reference

Global Substance Registration System

Nucleocidin (English)

14 October 2016

1 reference

UNII

F5097NG7JT

nucleocidin (English)

14 October 2016

1 reference

[(2S,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-2-fluoro-3,4-dihydroxytetrahydro-2-furanyl]methyl sulfamate (English)

14 October 2016

1 reference

Nucleocidin (English)

14 October 2016

ChEBI ID

166872

mapping relation type

exact match

2 references

ChEBI release 2021-03-01

International Chemical Identifier

InChI

InChI=1S/C10H13FN6O6S/c11-10(1-22-24(13,20)21)6(19)5(18)9(23-10)17-3-16-4-7(12)14-2-15-8(4)17/h2-3,5-6,9,18-19H,1H2,(H2,12,14,15)(H2,13,20,21)/t5-,6+,9-,10-/m1/s1

SureChEMBL ID

SCHEMBL3978671

2 references

based on heuristic

inferred from InChIKey

Global Substance Registration System

1 reference

0 references

2 references

UNII

F5097NG7JT

nucleocidin (English)

14 October 2016

Natural Product Atlas ID

NPA011799

2 references

based on heuristic

inferred from InChIKey