<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">133998</id>
  <title nil="true"/>
  <common-name>DiaPep 277</common-name>
  <description>DiaPep 277 is a polypeptide with the chemical formula C106H180N28O34. DiaPep 277 belongs to the polypeptides, a class of organic polymers within the organic compounds. With an average molecular weight of 2,391 g/mol, DiaPep 277 is a heavy molecule. It has been recorded as being found in or released from antennas within electrical and electronic equipment. In terms of biological activity, this compound acts as a modulator of the mitochondrial 60 kDa heat shock protein (HSPD1).</description>
  <cas>179822-83-4</cas>
  <pubchem-id>16138701</pubchem-id>
  <chemical-formula>C106H180N28O34</chemical-formula>
  <weight>2390.7</weight>
  <appearance nil="true"/>
  <melting-point nil="true"/>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility nil="true"/>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure nil="true"/>
  <target nil="true"/>
  <mechanism-of-toxicity nil="true"/>
  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity nil="true"/>
  <use-source nil="true"/>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2026-04-14T16:19:22Z</created-at>
  <updated-at type="dateTime">2026-08-26T17:09:46Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
  <kegg-compound-id nil="true"/>
  <omim-id nil="true"/>
  <chebi-id nil="true"/>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB06651</drugbank-id>
  <pdb-id nil="true"/>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>[H][C@](C)(O)[C@]([H])(N=C(O)[C@]([H])(CC(C)C)N=C(O)[C@]([H])(CO)N=C(O)[C@]([H])(CC(O)=O)N=C(O)[C@]([H])(CC(C)C)N=C(O)[C@]([H])(C)N=C(O)[C@]1([H])CCCN1C(=O)[C@@]([H])(N=C(O)[C@@]([H])(N=C(O)[C@]([H])(CCCNC(N)=N)N=C(O)[C@]([H])(CC(C)C)N=C(O)[C@]([H])(CC(C)C)N=C(O)[C@]([H])(C)N=C(O)[C@@]([H])(N=C(O)CN=C(O)CN=C(O)CN=C(O)[C@]([H])(CC(C)C)N=C(O)[C@@]([H])(N)C(C)C)C(C)C)C(C)C)[C@@]([H])(C)CC)C(=O)N1CCC[C@@]1([H])C(O)=N[C@@]([H])(C)C(O)=N[C@@]([H])(CC(O)=N)C(O)=N[C@@]([H])(CCC(O)=O)C(O)=N[C@@]([H])(CC(O)=O)C(O)=O</moldb-smiles>
  <moldb-formula>C106H180N28O34</moldb-formula>
  <moldb-inchi>InChI=1S/C106H180N28O34/c1-23-55(18)83(131-102(164)82(54(16)17)130-90(152)60(27-24-32-111-106(109)110)118-91(153)65(38-50(8)9)123-92(154)63(36-48(4)5)121-87(149)58(21)117-101(163)81(53(14)15)129-76(140)45-113-74(138)43-112-75(139)44-114-88(150)62(35-47(2)3)126-100(162)80(108)52(12)13)103(165)133-33-25-28-71(133)98(160)115-56(19)85(147)120-64(37-49(6)7)93(155)125-68(41-78(143)144)95(157)128-70(46-135)97(159)124-66(39-51(10)11)96(158)132-84(59(22)136)104(166)134-34-26-29-72(134)99(161)116-57(20)86(148)122-67(40-73(107)137)94(156)119-61(30-31-77(141)142)89(151)127-69(105(167)168)42-79(145)146/h47-72,80-84,135-136H,23-46,108H2,1-22H3,(H2,107,137)(H,112,139)(H,113,138)(H,114,150)(H,115,160)(H,116,161)(H,117,163)(H,118,153)(H,119,156)(H,120,147)(H,121,149)(H,122,148)(H,123,154)(H,124,159)(H,125,155)(H,126,162)(H,127,151)(H,128,157)(H,129,140)(H,130,152)(H,131,164)(H,132,158)(H,141,142)(H,143,144)(H,145,146)(H,167,168)(H4,109,110,111)/t55-,56-,57-,58-,59+,60-,61-,62-,63-,64-,65-,66-,67-,68-,69-,70-,71-,72-,80-,81-,82-,83-,84-/m0/s1</moldb-inchi>
  <moldb-inchikey>VGGRNGOEDNBLPH-YJHCMWSWSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">2390.768</moldb-average-mass>
  <moldb-mono-mass type="decimal">2389.321674988</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp>6.46</logp>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id nil="true"/>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM129891</chemdb-id>
  <dsstox-id nil="true"/>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id nil="true"/>
  <iupac>(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-({[(2S)-1-[(2S,3R)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-({[(2S)-1-[(2S,3S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[2-({2-[(2-{[(2S)-2-{[(2S)-2-amino-1-hydroxy-3-methylbutylidene]amino}-1-hydroxy-4-methylpentylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyethylidene}amino)-1-hydroxyethylidene]amino}-1-hydroxy-3-methylbutylidene]amino}-1-hydroxypropylidene]amino}-1-hydroxy-4-methylpentylidene]amino}-1-hydroxy-4-methylpentylidene]amino}-5-carbamimidamido-1-hydroxypentylidene]amino}-1-hydroxy-3-methylbutylidene]amino}-3-methylpentanoyl]pyrrolidin-2-yl](hydroxy)methylidene}amino)-1-hydroxypropylidene]amino}-1-hydroxy-4-methylpentylidene]amino}-3-carboxy-1-hydroxypropylidene]amino}-1,3-dihydroxypropylidene]amino}-1-hydroxy-4-methylpentylidene]amino}-3-hydroxybutanoyl]pyrrolidin-2-yl](hydroxy)methylidene}amino)-1-hydroxypropylidene]amino}-1-hydroxy-3-(C-hydroxycarbonimidoyl)propylidene]amino}-4-carboxy-1-hydroxybutylidene]amino}butanedioic acid</iupac>
  <moldb-polar-surface-area nil="true"/>
  <moldb-refractivity nil="true"/>
  <moldb-polarizability nil="true"/>
  <moldb-rotatable-bond-count nil="true"/>
  <moldb-acceptor-count nil="true"/>
  <moldb-donor-count nil="true"/>
  <moldb-pka-strongest-acidic nil="true"/>
  <moldb-pka-strongest-basic nil="true"/>
  <moldb-physiological-charge nil="true"/>
  <moldb-number-of-rings nil="true"/>
  <moldb-alogps-logp nil="true"/>
  <moldb-alogps-logs nil="true"/>
  <moldb-alogps-solubility nil="true"/>
  <kingdom>Organic compounds</kingdom>
  <superklass>Organic Polymers</superklass>
  <klass>Polypeptides</klass>
  <subklass nil="true"/>
  <paper-count type="integer">13</paper-count>
  <sync-id>CED0033192</sync-id>
  <structure-inchikey>VGGRNGOEDNBLPH-YJHCMWSWSA-N</structure-inchikey>
  <structure-fingerprint>40000010000200000000800800080400000800000000400044000042100020000000801003000080000000043004000004000000000000020004080020800000000010000000000004000000000100000020001000803000080005001000010000002000010000000000000000000002020002020100401100000100080000120a00000040200000022080000400040090001008000000800008000000000000012100000004000000050800002000000000080000100000048800000000000000800008000800000000000000000000000000050000010000408000100410400020000000400900000008000000010400000000010001000000000008000000</structure-fingerprint>
  <structure-pattern-fingerprint>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</structure-pattern-fingerprint>
  <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAACoAAAAqQAAAIABBiA0AAAAAQEEBgBgAAAA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</structure-pickle>
  <structure-indexed-at type="dateTime">2026-09-19T04:49:22Z</structure-indexed-at>
</compound>
