Muricarpone B
Grundinformationen
- CAS
886226-15-9- Standard-SMILES
O=C(CCCCc1ccc(O)c(O)c1)CCc1ccc(O)c(O)c1- InChIKey
UHRUXUCWHIGENP-UHFFFAOYSA-N- Summenformel
- C19H22O5
- Durchschnittliche Molmasse
- 330,4 g/mol
Überblick
1,7-bis(3,4-dihydroxyphenyl)heptan-3-one is a diarylheptanoid.
Namen und Bezeichner
- Bevorzugter Name
- Muricarpone B
- IUPAC
- 1,7-bis(3,4-dihydroxyphenyl)heptan-3-one
- Englischer Name
- Muricarpone B
- Summenformel
- C19H22O5
- Molmasse
- 330.38
Namen und Synonyme
Muricarpone B886226-15-9RefChem:9262271,7-bis(3,4-dihydroxyphenyl)heptan-3-oneorb1681029CHEMBL5286784SCHEMBL12659724ACon1_002176CHEBI:192667LKB22615TN5705AKOS040762864
Weitere Namen anzeigen
3-Heptanone, 1,7-bis(3,4-dihydroxyphenyl)-
Muricarpone B, >=85% (LC/MS-UV)NCGC00179754-01
Datenbank-Bezeichner
- CAS
886226-15-9- ChEMBL
CHEMBL5286784- ChEBI
CHEBI:192667- Nikkaji
- J2.257.771I
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 3,2
- Polarare Oberfläche (TPSA)
- 98 Ų
- H-Brücken-Donoren
- 4
- H-Brücken-Akzeptoren
- 5
- Frei drehbare Bindungen
- 8
- Schwere Atome
- 24
- Formalladung
- 0
- Komplexität
- 386
Physikochemische Eigenschaften
- Siedepunkt
- 615.1 · 615.1±55.0 °C(Predicted)
- Dichte
- 1.288 · 1.288±0.06 g/cm3(Predicted)
- storage temp.
- -20 °C · -20°C
- Löslichkeit
- 1 mg/mL · DMSO: 1mg/mL
- pka
- 9.77 · 9.77±0.10(Predicted)
- Aggregatzustand
- solid
- Major Application
- metabolomicsvitamins, nutraceuticals, and natural products
- InChI
- 1S/C19H22O5/c20-15(8-5-14-7-10-17(22)19(24)12-14)4-2-1-3-13-6-9-16(21)18(23)11-13/h6-7,9-12,21-24H,1-5,8H2
- InChIKey
- UHRUXUCWHIGENP-UHFFFAOYSA-N
- SMILES
- O=C(CCC1=CC(O)=C(C=C1)O)CCCCC2=CC=C(O)C(O)=C2
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
Sicherheitsdaten
- wgk
- WGK 3
- Speicherklasse
- 11 - Combustible Solids
Chemie und Industrie
Pharmakologische Informationen
MeSH Pharmacological Classification
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.
Agents that are used to treat allergic reactions. Most of these drugs act by preventing the release of inflammatory mediators or inhibiting the actions of released mediators on their target cells. (From AMA Drug Evaluations Annual, 1994, p475)
Anbieter9 Anbieter
Aladdin Scientific[email protected]
云南西力生物技术股份有限公司0871-65217109 · [email protected]
Labnetwork lnc.+86-27-50766799 +86-18062016861 · [email protected]
四川省维克奇生物科技有限公司028-81700200 18116577057 · [email protected]
上海博湖生物科技有限公司021-57763112 13585886131 · [email protected]
上海莫奇生物科技有限公司13341702378 · [email protected]
四川百奥克睿生物科技有限公司28-86-28-8543-3893 13260669172 · [email protected]
北京谱析科技有限公司400-808-7372 13161114455 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354 · [email protected]
Zugehörige Reaktionen
0
Keine Reaktionsaufzeichnungen unter den aktuellen Filterkriterien.
Notizen zur Verbindung
Wird geladen…