137875 <common-name>Satoreotide tetraxetan</common-name> <description>Satoreotide tetraxetan is a chemical compound with the formula C74H98ClN19O21S2. With an average molecular weight of 1,689 g/mol, Satoreotide tetraxetan is a heavy molecule.</description> <cas>1039726-31-2</cas> <pubchem-id nil="true"/> <chemical-formula>C74H98ClN19O21S2</chemical-formula> <weight nil="true"/> <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">2026-04-14T20:44:36Z</created-at> <updated-at type="dateTime">2026-05-14T19:57:39Z</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>DB16323</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@]1(NC(=O)[C@H](CCCCN)NC(=O)[C@@H](CC2=CC=C(NC(N)=O)C=C2)NC(=O)[C@H](CC2=CC=C(NC(=O)[C@@H]3CC(=O)NC(=O)N3)C=C2)NC(=O)[C@@H](CSSC[C@H](NC1=O)C(=O)N[C@H](CC1=CC=C(O)C=C1)C(N)=O)NC(=O)[C@H](CC1=CC=C(Cl)C=C1)NC(=O)CN1CCN(CC(O)=O)CCN(CC(O)=O)CCN(CC(O)=O)CC1)[C@@H](C)O</moldb-smiles> <moldb-formula>C74H98ClN19O21S2</moldb-formula> <moldb-inchi>InChI=1S/C74H98ClN19O21S2/c1-41(95)63-72(113)87-57(70(111)83-51(64(77)105)30-45-11-19-49(96)20-12-45)40-117-116-39-56(86-67(108)52(31-42-5-13-46(75)14-6-42)81-59(98)35-91-22-24-92(36-60(99)100)26-28-94(38-62(103)104)29-27-93(25-23-91)37-61(101)102)71(112)85-54(33-43-7-15-47(16-8-43)79-66(107)55-34-58(97)89-74(115)88-55)69(110)84-53(32-44-9-17-48(18-10-44)80-73(78)114)68(109)82-50(65(106)90-63)4-2-3-21-76/h5-20,41,50-57,63,95-96H,2-4,21-40,76H2,1H3,(H2,77,105)(H,79,107)(H,81,98)(H,82,109)(H,83,111)(H,84,110)(H,85,112)(H,86,108)(H,87,113)(H,90,106)(H,99,100)(H,101,102)(H,103,104)(H3,78,80,114)(H2,88,89,97,115)/t41-,50+,51-,52+,53?,54+,55+,56?,57?,63+/m1/s1</moldb-inchi> <moldb-inchikey>ZJZDXGQUNVNYQP-PBJKGYOGSA-N</moldb-inchikey> <moldb-average-mass type="decimal">1689.28</moldb-average-mass> <moldb-mono-mass type="decimal">1687.6314613</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>-10</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>CHEM133768</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>2-[4-({[(1S)-1-{[(4R,7S,10S,13R,16S,19S)-10-(4-aminobutyl)-4-{[(1R)-1-carbamoyl-2-(4-hydroxyphenyl)ethyl]carbamoyl}-13-{[4-(carbamoylamino)phenyl]methyl}-16-({4-[(4S)-2,6-dioxo-1,3-diazinane-4-amido]phenyl}methyl)-7-[(1R)-1-hydroxyethyl]-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaazacycloicosan-19-yl]carbamoyl}-2-(4-chlorophenyl)ethyl]carbamoyl}methyl)-7,10-bis(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]acetic 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 nil="true"/> <superklass nil="true"/> <klass nil="true"/> <subklass nil="true"/> <paper-count type="integer">98</paper-count> <sync-id>CED0019111</sync-id> <structure-inchikey>ZJZDXGQUNVNYQP-MXEXKMKYSA-N</structure-inchikey> <structure-fingerprint>4000000020400000002180000000140000080200000000010000008011000200010004300004122000020000102000001400200000001000006000000010000400000000400040040000000080000000002000201001400000000000804000000000000001008808841000400010000000000402010080040000040000020010002100804802042000000020000000008000100000000008000000088000000000000000c00000000000000008000000000000000000800000800002200c020001000000010008002000800000200000000010400000000000500220000020010000008008008000000040008000010490000000000002000000820000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle type="binary" encoding="base64">776t3gAAAAAQAAAAAwAAAAAAAAB1AAAAewAAAIABBiA0AAAAAQEEBwBoAAAA AwIBBgAoAAAAAwQIACgAAAADAgYgNAAAAAIBBAYAYAAAAAICBgBgAAAAAgIG AGAAAAACAgYAYAAAAAICBwBgAAAAAQIHAGgAAAADAgEGACgAAAADBAgAKAAA AAMCBiA0AAAAAQEEBgBgAAAAAgIGQCgAAAADBAZAaAAAAAMDAQZAaAAAAAMD AQZAKAAAAAMEBwBoAAAAAwIBBgAoAAAAAwQHAGgAAAADAQIIACgAAAADAgZA aAAAAAMDAQZAaAAAAAMDAQcAaAAAAAMCAQYAKAAAAAMECAAoAAAAAwIGIDQA AAACAQQGAGAAAAACAgZAKAAAAAMEBkBoAAAAAwMBBkBoAAAAAwMBBkAoAAAA AwQHAGgAAAADAgEGACgAAAADBAgAKAAAAAMCBiA0AAAAAgEEBgBgAAAAAgIG ACgAAAADBAgAKAAAAAMCBwBoAAAAAwIBBgAoAAAAAwQIACgAAAADAgcAaAAA AAMCAQZAaAAAAAMDAQZAaAAAAAMDAQcAaAAAAAMCAQYAKAAAAAMECAAoAAAA AwIGIDQAAAABAQQGAGAAAAACAhAAIAAAAAIQACAAAAACBgBgAAAAAgIGIDQA AAACAQQHAGgAAAADAgEGACgAAAADBAgAKAAAAAMCBgAoAAAAAwQIACgAAAAD AgcAaAAAAAMCAQYgNAAAAAIBBAYAYAAAAAICBkAoAAAAAwQGQGgAAAADAwEG QGgAAAADAwEGQCgAAAADBAgAaAAAAAMBAQZAaAAAAAMDAQZAaAAAAAMDAQYA KAAAAAMEBwBoAAAAAwECCAAoAAAAAwIHAGgAAAADAgEGACgAAAADBAgAKAAA AAMCBiA0AAAAAgEEBgBgAAAAAgIGQCgAAAADBAZAaAAAAAMDAQZAaAAAAAMD AQZAKAAAAAMEEQAgAAAAAQZAaAAAAAMDAQZAaAAAAAMDAQcAaAAAAAMCAQYA KAAAAAMECAAoAAAAAwIGAGAAAAACAgcAIAAAAAMGAGAAAAACAgYAYAAAAAIC BwAgAAAAAwYAYAAAAAICBgAoAAAAAwQIAGgAAAADAQEIACgAAAADAgYAYAAA AAICBgBgAAAAAgIHACAAAAADBgBgAAAAAgIGACgAAAADBAgAaAAAAAMBAQgA KAAAAAMCBgBgAAAAAgIGAGAAAAACAgcAIAAAAAMGAGAAAAACAgYAKAAAAAME CABoAAAAAwEBCAAoAAAAAwIGAGAAAAACAgYAYAAAAAICBiA0AAAAAQEEBgBg AAAAAQMIAGAAAAABAQsAAQABAiACAygCAgQABAUABQYABgcABwgACAkABAoA CgsgCwwoAgsNAA0OAA4PAA8QaAwQEWgMERJoDBITIBMUIBQVIBQWKAISF2gM FxhoDA0ZABkaIBobKAIaHAAcHQAdHgAeH2gMHyBoDCAhaAwhIiAiIyAjJCgC IyUAJSYAJicAJygoAicpICkqICorKAIqLCAhLWgMLS5oDBwvAC8wIDAxKAIw MgAyMwAzNAA0NQA1NgA2NwA3OAA4OSA5OigCNzsAOzwoAjs9ID0+AD4/AD9A AEBBaAxBQmgMQkNoDENEIENFaAxFRmgMPkcAR0ggR0koAjJKAEpLIEtMKAJL TQBNTgBOTwBPUGgMUFFoDFFSaAxSUwBSVGgMVFVoDE1WAFZXIFdYKAJXWQBZ WgBaWwBbXABcXQBdXgBeXwBfYCBfYSgCXWIAYmMAY2QAZGUAZWYAZmcgZmgo AmRpAGlqAGprAGtsAGxtAG1uIG1vKAJrcABwcQAAcgBycwBydAA5AABGQGgM VU9oDHFaABgPaAwuHmgMLCUAQgcAAAAUADk4NzY1NDMyMC8cGhkNCwoEAgEG EBESFxgPBh8gIS0uHgYmJykqLCUGQUJDRUZABlBRUlRVTwxbXF1iY2Rpamtw cVoXBAAAAAAAAAAW </structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:50:38Z</structure-indexed-at> </compound>