http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20070010817-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_52a24331fe7882d8a0801155df05d542
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-535
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K47-60
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-535
filingDate 2005-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39c3c61ae2ce788f23d4583f9106fc2e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1cd5e46d57b2984e07c8ad9d44be99b
publicationDate 2007-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20070010817-A
titleOfInvention Human Granulocyte Colony Stimulator Variants and Chemical Conjugates thereof
abstract The present invention relates to human granulocyte colony stimulating factor (G-CSF) variants and chemical conjugates thereof, which are used as an anticancer treatment aid, and the present invention relates to human granulocyte colony stimulating factor (G-CSF) comprising the amino acid sequence of SEQ ID NO: 1. Threonine (Thr) residue at position 133 of the residue is substituted with cysteine (Cys) residue, or cysteine residue (Cys) residue is inserted between Gly residue at position 135 and Ala residue at position 136 G-CSF variants and cysteine-introduced G-CSF variants in which these variants are conjugated with biocompatible polymers such as PEG to increase the retention time in the body without reducing biological activity and ultimately retain the activity in vivo. Provided are biocompatible polymer conjugates of the variants.
priorityDate 2005-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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