(0)C12P:1/2:
IPC6
SECTION C - CHEMISTRY; METALLURGY
FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A...
C12P
2/3
<<   >>   C12P009/00 - C12P019/64  

9
/ 00 Preparation of organic compounds containing a metal or atom other than H, N, C, O, S, or halogen [3]
 

11
/ 00 Preparation of sulfur-containing organic compounds [3]
 

13
/ 00 Preparation of nitrogen-containing organic compounds [3]

13
/ 02 Amides, e.g. chloramphenicol [3]  

13
/ 04 Alpha- or beta-amino acids [3]  

13
/ 06 Alanine; Leucine; Isoleucine; Serine; Homoserine [3]  

13
/ 08 Lysine; Diaminopimelic acid; Threonine; Valine [3]  

13
/ 10 Citrulline; Arginine; Ornithine [3]  

13
/ 12 Methionine; Cysteine; Cystine [3]  

13
/ 14 Glutamic acid; Glutamine [3]  

13
/ 16 using surfactants, fatty acids or fatty acid esters, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group or a carboxyl ester group [3]  

13
/ 18 using biotin or its derivatives [3]  

13
/ 20 Aspartic acid; Asparagine [3]  

13
/ 22 Tryptophan; Tyrosine; Phenylalanine; 3,4-Dihydroxyphenylalanine [3]  

13
/ 24 Proline; Hydroxyproline; Histidine [3]  
 

15
/ 00 Preparation of compounds containing at least three condensed carbocyclic rings [3]
 

17
/ 00 Preparation of heterocyclic carbon compounds with only O, N, S, Se, or Te as ring hetero atoms (C 12 P 13/04 to C 12 P 13/24 take precedence) [3]

17
/ 02 Oxygen as only ring hetero atoms [3]  

17
/ 04 containing a five-membered hetero ring, e.g. griseofulvin [3]  

17
/ 06 containing a six-membered hetero ring, e.g. fluorescein [3]  

17
/ 08 containing a hetero ring of at least seven ring members, e.g. zearalenone, macrolide aglycons [3]  

17
/ 10 Nitrogen as only ring hetero atom [3]  

17
/ 12 containing a six-membered hetero ring [3]  

17
/ 14 Nitrogen or oxygen as hetero atom and at least one other diverse hetero ring atom in the same ring [3]  

17
/ 16 containing two or more hetero rings [3]  

17
/ 18 containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin [3]  
 

19
/ 00 Preparation of compounds containing saccharide radicals (ketoaldonic acids C 12 P 7/58) [3]

Note

 

Attention is drawn to Note (3) following the title of subclass C 07 H, which defines the expression "saccharide radical". [3]

19
/ 02 Monosaccharides (2-ketogulonic acid C 12 P 7/60) [3]  

19
/ 04 Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds [3]  

19
/ 06 Xanthan, i.e. Xanthomonas-type heteropolysaccharides [3]  

19
/ 08 Dextran [3]  

19
/ 10 Pullulan [3]  

19
/ 12 Disaccharides [3]  

19
/ 14 produced by the action of a carbohydrase, e.g. by alpha-amylase [3]  

19
/ 16 produced by the action of an alpha-1, 6-glucosidase, e.g. amylose, debranched amylopectin (non-biological hydrolysis of starch C 08 B 30/00) [3]  

19
/ 18 produced by the action of a glycosyl transferase, e.g. alpha-, beta- or gamma-cyclodextrins [3]  

19
/ 20 produced by the action of an exo-1, 4 alpha-glucosidase, e.g. dextrose [3]  

19
/ 22 produced by the action of a beta-amylase, e.g. maltose [3]  

19
/ 24 produced by the action of an isomerase, e.g. fructose [3]  

19
/ 26 Preparation of nitrogen-containing carbohydrates [3]  

19
/ 28 N-glycosides [3]  

19
/ 30 Nucleotides [3]  

19
/ 32 having a condensed ring system containing a six-membered ring having two nitrogen atoms in the same-ring, e.g. purine nucleotides, nicotineamide-adenine dinucleotide [3]  

19
/ 34 Polynucleotides, e.g. nucleic acids, oligoribonucleotides [3]  

19
/ 36 Dinucleotides, e.g. nicotineamide-adenine dinucleotide phosphate [3]  

19
/ 38 Nucleosides [3]  

19
/ 40 having a condensed ring system containing a six-membered ring having two nitrogen atoms in the same ring, e.g. purine nucleosides [3]  

19
/ 42 Cobalamins, i.e. vitamin B12 , LLD factor [3]  

19
/ 44 Preparation of O-glycosides, e.g. glucosides [3]  

19
/ 46 having an oxygen atom of the saccharide radical bound to a cyclohexyl radical, e.g. kasugamycin [3]  

19
/ 48 the cyclohexyl radical being substituted by two or more nitrogen atoms, e.g. destomycin, neamin [3]  

19
/ 50 having two saccharide radicals bound through only oxygen to adjacent ring carbon atoms of the cyclohexyl radical, e.g. ambutyrosin, ribostamycin [3]  

19
/ 52 containing three or more saccharide radicals, e.g. neomycin, lividomycin [3]  

19
/ 54 the cyclohexyl radical being bound directly to a nitrogen atom of two or more radicals, e.g. streptomycin [3]  

19
/ 56 having an oxygen atom of the saccharide radical directly bound to a condensed ring system having three or more carbocyclic rings, e.g. daunomycin, adriamycin [3]  

19
/ 58 having an oxygen atom of the saccharide radical directly bound through only acyclic carbon atoms to a non-saccharide heterocyclic ring, e.g. bleomycin, phleomycin [3]  

19
/ 60 having an oxygen of the saccharide radical directly bound to a non-saccharide heterocyclic ring or a condensed ring system containing a non-saccharide heterocyclic ring, e.g. coumermycin, novobiocin [3]  

19
/ 62 the hetero ring having eight or more ring members and only oxygen as ring hetero atoms, e.g. erythromycin, spiramycin, nystatin [3]  

19
/ 64 Preparation of S-glycosides, e.g. lincomycin [3]  

<< >>
1 2 3