(Q27128676)

Streptothricin F (English)

(2R,3S,4R,5R,6R)-6-{[(3aS,7R,7aS)-7-hydroxy-4-oxo-1H,3aH,5H,6H,7H,7aH-imidazo[4,5-c]pyridin-2-yl]amino}-5-[(3S)-3,6-diaminohexanamido]-4-hydroxy-2-(hydroxymethyl)oxan-3-yl carbamate

6 October 2016

stereoisomer of

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₁₉H₃₄N₈O₈

1 reference

Streptothricin F (English)

6 October 2016

canonical SMILES

C1C(C2C(C(=O)N1)N=C(N2)NC3C(C(C(C(O3)CO)OC(=O)N)O)NC(=O)CC(CCCN)N)O

1 reference

Streptothricin F (English)

6 October 2016

isomeric SMILES

C1[C@H]([C@@H]2[C@@H](C(=O)N1)N=C(N2)N[C@H]3[C@@H]([C@@H]([C@H]([C@H](O3)CO)OC(=O)N)O)NC(=O)C[C@H](CCCN)N)O

1 reference

Streptothricin F (English)

Streptomyces griseochromogenes

6 October 2016

found in taxon

1 reference

[2,3,4,6,6-2H5]-d-glucose as a general probe for sugar transformations in microbial metabolism: Application to the biosynthesis of sarubicin A, blasticidin S, and streptothricin F

Streptomyces nojiriensis

1 reference

New streptothricin-group antibiotics, AN-201 I, II and III. II. Chemical structures

Streptomyces

3 references

Biosynthesis of streptothricin F. 5. Formation of .beta.-lysine by Streptomyces L-1689-23

Biosynthesis of streptothricin F

The biosynthesis of the streptolidine moiety in streptothricin F

Streptomyces lavendulae

5 references

Biosynthesis of streptothricin F. Part 6. Formation and intermediacy of D-glucosamine in Streptomyces L-1689-23

Purification and biochemical characterization of streptothricin acetyltransferase coded by the cloned streptothricin-resistance gene of Streptomyces lavendulae

Nucleotide sequence of the streptothricin acetyltransferase gene from Streptomyces lavendulae and its expression in heterologous hosts

Isolation and characterization of a pock-forming plasmid pTA4001 from Streptomyces lavendulae.

Yazumycin, a new antibiotic produced by Streptomyces lavendulae

Streptomyces noursei

1 reference

Influence of inorganic phosphate on the lipid synthesis of a phosphate-deregulated mutant of Streptomyces noursei

Streptomyces rochei

1 reference

A silent ABC transporter isolated from Streptomyces rochei F20 induces multidrug resistance.

Streptomyces qinlingensis

1 reference

Two new members of streptothricin class antibiotics from Streptomyces qinlingensis sp. nov.

Identifiers

InChI

InChI=1S/C19H34N8O8/c20-3-1-2-7(21)4-10(30)24-13-14(31)15(35-18(22)33)9(6-28)34-17(13)27-19-25-11-8(29)5-23-16(32)12(11)26-19/h7-9,11-15,17,28-29,31H,1-6,20-21H2,(H2,22,33)(H,23,32)(H,24,30)(H2,25,26,27)/t7-,8+,9+,11+,12-,13+,14-,15-,17+/m0/s1

1 reference

Streptothricin F (English)

NRAUADCLPJTGSF-VLSXYIQESA-N

6 October 2016

InChIKey

2 references

Streptothricin F (English)

6 October 2016

ChEBI release 2020-09-01

2 references

https://commonchemistry.cas.org/detail?cas_rn=3808-42-2

streptothricin F (English)

6 October 2016

5 April 2021

InChIKey

NRAUADCLPJTGSF-VLSXYIQESA-N

1 reference

Yazumycin A (English)

6 October 2016

1 reference

Streptothricin F (English)

6 October 2016

Reaxys registry number

6031385

1 reference

streptothricin F (English)

6 October 2016

ChEBI ID

60821

mapping relation type

1 reference