StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
Huagongshe Open Project:[email protected]KI-Anbindung: llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.7.8
  1. Startseite
  2. /Verbindung

Didemnin C

HCID 9963211
NotizenReaktionen
GrundinformationenÜberblickNamen und BezeichnerEigenschaftenChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
TeilstruktursucheÄhnliche Strukturen suchen

Grundinformationen

CAS
77327-06-1
Standard-SMILES
CC[C@H](C)[C@H]1NC(=O)[C@@H](NC(=O)[C@@H](CC(C)C)N(C)C(=O)[C@H](C)O)[C@@H](C)OC(=O)[C@H](Cc2ccc(OC)cc2)N(C)C(=O)[C@@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@@H](C)C(=O)[C@H](C(C)C)OC(=O)C[C@@H]1O
InChIKey
ZRSXZCRRAOVIJD-UHFFFAOYSA-N
Summenformel
C52H82N6O14
Durchschnittliche Molmasse
1.015,2 g/mol
Monoisotopische Masse
1.014,58890131

Überblick

Didemnin C is an organic molecular entity.

Namen und Bezeichner

Bevorzugter Name
Didemnin C
IUPAC
(2R)-N-[(3S,6S,8S,12S,13R,16S,17R,20S,23S)-13-[(2S)-butan-2-yl]-12-hydroxy-20-[(4-methoxyphenyl)methyl]-6,17,21-trimethyl-3-(2-methylpropyl)-2,5,7,10,15,19,22-heptaoxo-8-propan-2-yl-9,18-dioxa-1,4,14,21-tetrazabicyclo[21.3.0]hexacosan-16-yl]-2-[[(2S)-2-hydroxypropanoyl]-methylamino]-4-methylpentanamide
Englischer Name
N-(L-Lac-N-Methyl-D-Leu-)cyclo[L-Thr*-[(3S,4R)-3-hydroxy-4-[(S)-1-methylpropyl]-γAbu-]-[(2S,4S)-4-hydroxy*-2,5-dimethyl-2-deamino-3-oxo-D-Nle-]-L-Leu-L-Pro-N,O-dimethyl-L-Tyr-]
Summenformel
C52H82N6O14
Molmasse
1015.26

Namen und Synonyme

Didemnin C77327-06-1Didemnin A, N-(2-hydroxy-1-oxopropyl)-, (S)-68SK86968R(2R)-N-[(3S,6S,8S,12S,13R,16S,17R,20S,23S)-13-[(2S)-butan-2-yl]-12-hydroxy-20-[(4-methoxyphenyl)methyl]-6,17,21-trimethyl-3-(2-methylpropyl)-2,5,7,10,15,19,22-heptaoxo-8-propan-2-yl-9,18-dioxa-1,4,14,21-tetrazabicyclo[21.3.0]hexacosan-16-yl]-2-[[(2S)-2-hydroxypropanoyl]-methylamino]-4-methylpentanamide(2R)-N-((3S,6S,8S,12S,13R,16S,17R,20S,23S)-13-((2S)-butan-2-yl)-12-hydroxy-20-((4-methoxyphenyl)methyl)-6,17,21-trimethyl-3-(2-methylpropyl)-2,5,7,10,15,19,22-heptaoxo-8-propan-2-yl-9,18-dioxa-1,4,14,21-tetrazabicyclo(21.3.0)hexacosan-16-yl)-2-(((2S)-2-hydroxypropanoyl)-methylamino)-4-methylpentanamideRefChem:133285(2R)-N-((3S,6S,8S,12S,13R,16S,17R,20S)-13-((2S)-butan-2-yl)-20-((4-methoxyphenyl)methyl)-6,12,17,21-tetramethyl-3-(2-methylpropyl)-2,5,7,10,15,19,22-heptaoxo-8-propan-2-yl-9,18-dioxa-1,4,14,21-tetrazabicyclo(21.3.0)hexacosan-16-yl)-2-(2-hydroxypropanoyl(methyl)amino)-4-methylpentanamide

Eigenschaften

Berechnete Struktureigenschaften

XLogP
5,5
Polarare Oberfläche (TPSA)
268 Ų
H-Brücken-Donoren
5
H-Brücken-Akzeptoren
14
Frei drehbare Bindungen
14
Schwere Atome
72
Formalladung
0
Komplexität
1.890

Physikochemische Eigenschaften

Siedepunkt
1195.4 · 1195.4±65.0 °C(Predicted)
Dichte
1.22 · 1.22±0.1 g/cm3(Predicted)
pka
11.28 · 11.28±0.70(Predicted)

Chemie und Industrie

Pharmakologische Informationen

MeSH Pharmacological Classification · 4 Einträge

Substances that prevent infectious agents or organisms from spreading or kill infectious agents in order to prevent the spread of infection.

Substances that inhibit or prevent the proliferation of NEOPLASMS.

Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly.

Agents that suppress immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-CELLS or by inhibiting the activation of HELPER CELLS. While immunosuppression has been brought about in the past primarily to prevent rejection of transplanted organs, new applications involving mediation of the effects of INTERLEUKINS and other CYTOKINES are emerging.

Anbieter2 Anbieter

上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
TargetMol中国(陶术生物)15002134094 · [email protected]

Zugehörige Reaktionen

0
Reaktionsaufzeichnung erstellen

Keine Reaktionsaufzeichnungen unter den aktuellen Filterkriterien.

Notizen zur Verbindung

Wird geladen…

Auf dieser SeiteGrundinformationenÜberblickNamen und BezeichnerEigenschaftenChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
(2R)-N-((3S,6S,8S,12S,13R,16S,17R,20S,23S)-13-((2S)-butan-2-yl)-12-hydroxy-20-((4-methoxyphenyl)methyl)-6,17,21-trimethyl-3-(2-methylpropyl)-2,5,7,10,15,19,22-heptaoxo-8-propan-2-yl-9,18-dioxa-1,4,14,21-tetrazabicyclo(21.3.0)hexacosan-16-yl)-2-(2-hydroxypropanoyl(methyl)amino)-4-methylpentanamide
N-(12-hydroxy-20-((4-methoxyphenyl)methyl)-6,17,21-trimethyl-3,13-bis(2-methylpropyl)-2,5,7,10,15,19,22-heptaoxo-8-propan-2-yl-9,18-dioxa-1,4,14,21-tetrazabicyclo(21.3.0)hexacosan-16-yl)-2-(2-hydroxypropanoyl(methyl)amino)-4-methylpentanamide
UNII-68SK86968R
DIDEMNIN C [MI]
Weitere Namen anzeigen
N-(L-Lac-N-Methyl-D-Leu-)cyclo[L-Thr*-[(3S,4R)-3-hydroxy-4-[(S)-1-methylpropyl]-γAbu-]-[(2S,4S)-4-hydroxy*-2,5-dimethyl-2-deamino-3-oxo-D-Nle-]-L-Leu-L-Pro-N,O-dimethyl-L-Tyr-]L-Tyrosine, N-[(2S)-2-hydroxy-1-oxopropyl]-N-methyl-D-leucyl-L-threonyl-(3S,4R,5S)-4-amino-3-hydroxy-5-methylheptanoyl-(2S,4S)-4-hydroxy-2,5-dimethyl-3-oxohexanoyl-L-leucyl-L-prolyl-N,O-dimethyl-, (7→2)-lactone
CHEMBL505317CHEBI:231128(R)-N-((3S,6R,7S,10R,11S,15S,17S,20S,25aS)-10-((S)-sec-butyl)-11-hydroxy-20-isobutyl-15-isopropyl-3-(4-methoxybenzyl)-2,6,17-trimethyl-1,4,8,13,16,18,21-heptaoxodocosahydro-15H-pyrrolo[2,1-f][1,15]dioxa[4,7,10,20]tetraazacyclotricosin-7-yl)-2-((S)-2-hydroxy-N-methylpropanamido)-4-methylpentanamideL-Tyrosine, (2S)-2-hydroxypropanoyl-N-Methyl-D-leucyl-L-threonyl-(3S,4R,5S)-4-amino-3-hydroxy-5-methylheptanoyl-(2S,4S)-4-hydroxy-2,5-dimethyl-3-oxohexanoyl-L-leucyl-L-prolyl-N,O-dimethyl-, (8-3)-lactoneHY-130564Q27264273L-TYROSINE, N-((2S)-2-HYDROXY-1-OXOPROPYL)-N-METHYL-D-LEUCYL-L-THREONYL-(3S,4R,5S)-4-AMINO-3-HYDROXY-5-METHYLHEPTANOYL-(2S,4S)-4-HYDROXY-2,5-DIMETHYL-3-OXOHEXANOYL-L-LEUCYL-L-PROLYL-N,O-DIMETHYL-, (7->2)-LACTONE

Datenbank-Bezeichner

CAS
77327-06-1
PubChem CID
9963211
ChEMBL
CHEMBL505317
ChEBI
CHEBI:231128
UNII
68SK86968R