HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HCID 16137828Erstellt: 25. Oktober 2026
Tesamorelin
Tesamorelin · Adipotide/FTTP · tesamorel · Tesamorelin 5mg/10mg/20mg · TSM2 · D06655 · Tirelin · Timorelin
https://huagongshe.com/de/chemical/16137828

Identifikatoren & physikalische Daten
| CAS No. | 218949-48-5 |
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| Summenformel | C221H366N72O67S |
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| Durchschnittliche Molmasse | 5.136 g/mol |
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| Monoisotopische Masse | 5.132,71664025 g/mol |
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| SMILES | CC/C=C/CC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC(C)C)C(N)=O)[C@@H](C)CC)C(C)C)[C@@H](C)O)[C@@H](C)CC |
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| InChIKey | QBEPNUQJQWDYKU-BMGKTWPMSA-N |
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| PubChem CID | 16137828 |
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| ChEMBL | CHEMBL1237026 |
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| DTXSID | DTXSID00583207 |
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Chemische & physikalische Eigenschaften
| XLogP | -23,3 |
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| Polarare Oberfläche (TPSA) | 2.360 |
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| H-Brücken-Donoren | 83 |
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| H-Brücken-Akzeptoren | 76 |
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| Frei drehbare Bindungen | 187 |
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| Schwere Atome | 361 |
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| Formalladung | 0 |
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| Komplexität | 12.800 |
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| Biologics | Biologic product (Egrifta) -> FDA Purple BookBiologic product (Egrifta SV) -> FDA Purple BookBiologic product (Egrifta WR) -> FDA Purple Book |
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| Lagerbedingungen | 2-8°C Refrigerator |
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Sicherheit & Vorschriften
| Hepatotoxicity | In clinical trials in patients with HIV-associated lipodystrophy, tesamorelin therapy was not associated with de novo elevations in serum enzymes and, in some studies, was associated with decreases in preexisting ALT elevations, possibly mediated by improvements in nonalcoholic fatty liver. Instances of clinically apparent liver injury attributable to tesamorelin use have not been reported. |
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