US PATENT SUBCLASS 536 / 27.13
.~.~.~.~.~ Bicyclic ring system consisting of the N-hetero ring fused to another hetero ring (e.g., 2-azaadenines, 6-azaadenines, etc.)


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536 /   HD   ORGANIC COMPOUNDS -- PART OF THE CLASS 532-570 SERIES

*  DD  ORGANIC COMPOUNDS (Class 532, Subclass 1) {1}
1.11  DF  .~ Carbohydrates or derivatives {15}
18.7  DF  .~.~ Nitrogen containing {13}
22.1  DF  .~.~.~ N-glycosides, polymers thereof, metal derivatives (e.g., nucleic acids, oligonucleotides, etc.) {12}
27.1  DF  .~.~.~.~ N-glycosides wherein the N is part of an N-hetero ring which hetero ring is part of a polycyclo ring system containing an N-hetero ring and an additional hetero ring (e.g., rebeccamycin, etc.) {3}
27.13.~.~.~.~.~ Bicyclic ring system consisting of the N-hetero ring fused to another hetero ring (e.g., 2-azaadenines, 6-azaadenines, etc.) {2}
27.14  DF  .~.~.~.~.~.~> Multideoxy or didehydro
27.2  DF  .~.~.~.~.~.~> The bicyclic ring system consists of a 1,3-diazine ring, which may be hydrogenated, fused to a five-membered N-hetero ring (e.g., purine isoesters like tubercidin, toyocamycin, sangivamycin, sparsomycin A, etc.) {1}


DEFINITION

Classification: 536/27.13

Bicyclic ring system consisting of the N-hetero ring fused to another hetero ring (e.g., 2-azaadenines, 6-azaadenines, etc.):

(under subclass 27.1) Compounds wherein the N-hetero ring is part of a bicyclic ring system which consists of an N-hetero ring fused to another hetero ring.

(1) Note. Examples of compounds provided for herein are: [figure] [figure] [figure]