Browse result page of B3Pdb

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B3pdbIDb3pdb_0066PEPTIDE NAMEHAVN1PEPTIDE SEQUENCE (1-letter)SHAVSSPEPTIDE SEQUENCE (3-letter)SerHisAlaValSerSerN-TERMINAL MODIFICATIONNAC-TERMINAL MODIFICATION NACHEMICAL MODIFICATIONNAPEPTIDE LENGTH6PEPTIDE CONFORMATIONCyclicPEPTIDE NATURENASOURCE/ORIGIN OF PEPTIDEChemically synthesizedSMILESN[C@@]([H])(CO)C(=O)N[C@@]([H])(CC1=CN=C-N1)C(=O)N[C@@]([H])(C)C(=O)N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])(CO)C(=O)N[C@@]([H])(CO)C(=O)OCELL LINENAIn vitro CONCENTRATIONNAIn vitro METHODNAIn vitro RESULTNAANIMAL MODELC57BL6 miceIn vivo CONCENTRATIONNAIn vivo MODE OF DELIVERYIntracerebral ventricularIn vivo METHODMass SpectromteryIn vivo RESULTIt is able to deliver an IRdye800CW-labeled IgG monoclonal antibody into the brain. ACTIONSynthesized novel cyclic peptides are able efectively modulate the BBB to enhance the delivery of mA TRANSPORT TYPENA SUBCELLULAR LOCALISATIONNA COMBINATIONCombined with monoclonal antibody PHYSICAL CONDITIONNA RESPONSENA RESULTNA LABELNAPMID 31683745
B3pdbIDb3pdb_0067PEPTIDE NAMEHAVN2PEPTIDE SEQUENCE (1-letter)SHAVSPEPTIDE SEQUENCE (3-letter)SerHisAlaValSerN-TERMINAL MODIFICATIONNAC-TERMINAL MODIFICATION NACHEMICAL MODIFICATIONNAPEPTIDE LENGTH5PEPTIDE CONFORMATIONCyclicPEPTIDE NATURENASOURCE/ORIGIN OF PEPTIDEChemically synthesizedSMILESN[C@@]([H])(CO)C(=O)N[C@@]([H])(CC1=CN=C-N1)C(=O)N[C@@]([H])(C)C(=O)N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])(CO)C(=O)OCELL LINENAIn vitro CONCENTRATIONNAIn vitro METHODNAIn vitro RESULTNAANIMAL MODELC57BL6 miceIn vivo CONCENTRATIONNAIn vivo MODE OF DELIVERYIntracerebral ventricularIn vivo METHODMass SpectromteryIn vivo RESULTIt is able to deliver an IRdye800CW-labeled IgG monoclonal antibody into the brain. ACTIONSynthesized novel cyclic peptides are able efectively modulate the BBB to enhance the delivery of mA TRANSPORT TYPENA SUBCELLULAR LOCALISATIONNA COMBINATIONCombined with monoclonal antibody PHYSICAL CONDITIONNA RESPONSENA RESULTNA LABELNAPMID 31683745
B3pdbIDb3pdb_0068PEPTIDE NAMELinear ADTHAVPEPTIDE SEQUENCE (1-letter)TPPVSHAVPEPTIDE SEQUENCE (3-letter)ThrProProValSerHisAlaValN-TERMINAL MODIFICATIONAcetylaed at N-terminalC-TERMINAL MODIFICATION Amide group is attached at C-terminalCHEMICAL MODIFICATIONNAPEPTIDE LENGTH8PEPTIDE CONFORMATIONLinearPEPTIDE NATURENASOURCE/ORIGIN OF PEPTIDEChemically synthesizedSMILESN[C@@]([H])([C@]([H])(O)C)C(=O)N1[C@@]([H])(CCC1)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])(CO)C(=O)N[C@@]([H])(CC1=CN=C-N1)C(=O)N[C@@]([H])(C)C(=O)N[C@@]([H])(C(C)C)C(=O)OCELL LINENAIn vitro CONCENTRATIONNAIn vitro METHODNAIn vitro RESULTNAANIMAL MODELC57BL6 miceIn vivo CONCENTRATIONNAIn vivo MODE OF DELIVERYIntracerebral ventricularIn vivo METHODMass SpectromteryIn vivo RESULTIt is able to deliver an IRdye800CW-labeled IgG monoclonal antibody into the brain. ACTIONSynthesized novel cyclic peptides are able efectively modulate the BBB to enhance the delivery of mA TRANSPORT TYPENA SUBCELLULAR LOCALISATIONNA COMBINATIONCombined with monoclonal antibody PHYSICAL CONDITIONNA RESPONSENA RESULTNA LABELNAPMID 31683745
B3pdbIDb3pdb_0069PEPTIDE NAMECyclic ADTHAVPEPTIDE SEQUENCE (1-letter)TPPVSHAVPEPTIDE SEQUENCE (3-letter)ThrProProValSerHisAlaValN-TERMINAL MODIFICATIONNAC-TERMINAL MODIFICATION NACHEMICAL MODIFICATIONNAPEPTIDE LENGTH8PEPTIDE CONFORMATIONCyclicPEPTIDE NATURENASOURCE/ORIGIN OF PEPTIDEChemically synthesizedSMILESN[C@@]([H])([C@]([H])(O)C)C(=O)N1[C@@]([H])(CCC1)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])(CO)C(=O)N[C@@]([H])(CC1=CN=C-N1)C(=O)N[C@@]([H])(C)C(=O)N[C@@]([H])(C(C)C)C(=O)OCELL LINENAIn vitro CONCENTRATIONNAIn vitro METHODNAIn vitro RESULTNAANIMAL MODELC57BL6 miceIn vivo CONCENTRATIONNAIn vivo MODE OF DELIVERYIntracerebral ventricularIn vivo METHODMass SpectromteryIn vivo RESULTIt is able to deliver an IRdye800CW-labeled IgG monoclonal antibody into the brain. ACTIONSynthesized novel cyclic peptides are able efectively modulate the BBB to enhance the delivery of mA TRANSPORT TYPENA SUBCELLULAR LOCALISATIONNA COMBINATIONCombined with monoclonal antibody PHYSICAL CONDITIONNA RESPONSENA RESULTNA LABELNAPMID 31683745
B3pdbIDb3pdb_0070PEPTIDE NAMEADTC5PEPTIDE SEQUENCE (1-letter)CDTPPVCPEPTIDE SEQUENCE (3-letter)CysAspThrProProValCysN-TERMINAL MODIFICATIONNAC-TERMINAL MODIFICATION Amide group is attached at C-terminalCHEMICAL MODIFICATIONNAPEPTIDE LENGTH7PEPTIDE CONFORMATIONCyclicPEPTIDE NATURENASOURCE/ORIGIN OF PEPTIDEChemically synthesizedSMILESN[C@@]([H])(CS)C(=O)N[C@@]([H])(CC(=O)O)C(=O)N[C@@]([H])([C@]([H])(O)C)C(=O)N1[C@@]([H])(CCC1)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])(CS)C(=O)OCELL LINENAIn vitro CONCENTRATIONNAIn vitro METHODNAIn vitro RESULTNAANIMAL MODELC57BL6 miceIn vivo CONCENTRATIONNAIn vivo MODE OF DELIVERYIntracerebral ventricularIn vivo METHODMass SpectromteryIn vivo RESULTIt is able to deliver an IRdye800CW-labeled IgG monoclonal antibody into the brain. ACTIONSynthesized novel cyclic peptides are able efectively modulate the BBB to enhance the delivery of mA TRANSPORT TYPENA SUBCELLULAR LOCALISATIONNA COMBINATIONCombined with monoclonal antibody PHYSICAL CONDITIONNA RESPONSENA RESULTNA LABELNAPMID 31683745