Phellopterin - ≥99% , CAS No.2543-94-4

CAS: 2543-94-4 Cat. No.: P649249 Summenformel: C17H16O5 Molekulargewicht: 300.31 EG-Nummer: 110-046-4
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QUALITÄT & REINHEIT ≥99%
Synonyms
Q3742334 | NSC 152469 | NSC152469 | NSC-152469 | Methanesulfinic acid, 1,1,1-trifluoro-, sodium salt (1:1) | 4-Methoxy-9-prenyloxypsoralen | C17047 | HMS2203M11 | Phelloptorin | NCGC00247535-01 | 4-Methoxy-9-((3-methylbut-2-en-1-yl)oxy)-7H-furo[3,2-g]chro
Storage
Protected from light,Store at -20°C
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P649249-5mg
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347,88€
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590,84€
25mg
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Warum diese Qualität

≥99% für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Protected from light,Store at -20°C Versand Ice chest + Ice pads. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Literaturbeleg

In 0 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

Phellopterin is a natural product isolated from Angelica dahurica. Phellopterin reduces TNF-alpha-induced VCAM-1 expression through regulation of the Akt and PKC pathway, which contributes to inhibit the adhesion of monocytes to endothelium.

Form:Solid

Spezifikationen

Synonyme
Q3742334 | NSC 152469 | NSC152469 | NSC-152469 | Methanesulfinic acid, 1,1,1-trifluoro-, sodium salt (1:1) | 4-Methoxy-9-prenyloxypsoralen | C17047 | HMS2203M11 | Phelloptorin | NCGC00247535-01 | 4-Methoxy-9-((3-methylbut-2-en-1-yl)oxy)-7H-furo[3,2-g]chro
Spezifikationen & Reinheit
≥99%
Biochemische und physiologische Mechanismen
Phellopterin is a natural product isolated from Angelica dahurica . Phellopterin reduces TNF-alpha-induced VCAM-1 expression through regulation of the Akt and PKC pathway, which contributes to inhibit the adhesion of monocytes to endothelium.
Storage
Protected from light,Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥99%
Namen und Kennungen
Pubchem Sid
Kanonisches Lächeln
COc1c2ccoc2c(OCC=C(C)C)c2oc(=O)ccc12
IUPAC Name
4-methoxy-9-(3-methylbut-2-enoxy)furo[3,2-g]chromen-7-one
InChIKey
BMLZFLQMBMYVHG-UHFFFAOYSA-N
INCHI
1S/C17H16O5/c1-10(2)6-8-21-17-15-12(7-9-20-15)14(19-3)11-4-5-13(18)22-16(11)17/h4-7,9H,8H2,1-3H3
Isomere SMILES
CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C
Alternative CAS-Nummer
2543-94-4
NSC-Nummer
152469
MeSH-Eintrag
phellopterin
Molekulargewicht
300.31

Dokumentation

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✅ Analysezertifikat (COA)

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassPhenylpropanoids and polyketides
KlasseCoumarins and derivatives
SubclassFuranocoumarins
Intermediate Tree Nodes Linear furanocoumarins - Psoralens
Direct Parent5-methoxypsoralens
Alternative Parents 1-benzopyrans  Benzofurans  Anisoles  Pyranones and derivatives  Alkyl aryl ethers  Heteroaromatic compounds  Furans  Lactones  Oxacyclic compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 5-methoxypsoralen - Benzopyran - 1-benzopyran - Benzofuran - Anisole - Alkyl aryl ether - Pyranone - Pyran - Benzenoid - Furan - Heteroaromatic compound - Lactone - Oxacycle - Ether - Organoheterocyclic compound - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as 5-methoxypsoralens. These are psoralens containing a methoxy group attached at the C5 position of the psoralen group.
External Descriptors psoralens
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
CYP1A2 Tchem Cytochrome P450 1A2 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP1B1 Tchem Cytochrome P450 1B1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP1A1 Tchem Cytochrome P450 1A1 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP1B1 Tchem Cytochrome P450 1B1 (1148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A1 Tchem Cytochrome P450 1A1 (1169 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
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CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
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GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)
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G6PD Tchem Glucose-6-phosphate 1-dehydrogenase (778 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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SNCA Tchem Alpha-synuclein (10960 Activities)
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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MBNL1 Tbio Muscleblind-like protein 1 (34431 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TARDBP Tchem TAR DNA-binding protein 43 (40113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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norA Quinolone resistance protein norA (2171 Activities)
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Mapt Microtubule-associated protein tau (6 Activities)
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PA Polymerase acidic protein (806 Activities)
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fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NS1 Nonstructural protein 1 (33327 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
G6PD-6PGL Glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase (1761 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gabrg2 GABA-A receptor; alpha-1/beta-2/gamma-2 (554 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
mdeA Fluoroquinolone resistance protein (28 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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8 results found

Lot NumberCertificate TypeDatumArtikel
C2504272C2504272Certificate of AnalysisFeb 25, 2025 P649249
C2504273C2504273Certificate of AnalysisFeb 25, 2025 P649249
C2504286C2504286Certificate of AnalysisFeb 25, 2025 P649249
C2504294C2504294Certificate of AnalysisFeb 25, 2025 P649249
C2504295C2504295Certificate of AnalysisFeb 25, 2025 P649249
C2504296C2504296Certificate of AnalysisFeb 25, 2025 P649249
C2504297C2504297Certificate of AnalysisFeb 25, 2025 P649249
C2504316C2504316Certificate of AnalysisFeb 25, 2025 P649249
Chemische und physikalische Eigenschaften
LöslichkeitDMSO : 100 mg/mL (332.99 mM; Need ultrasonic)
EmpfindlichkeitLight sensitive
Molekulargewicht300.300 g/mol
XLogP33.800
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass300.1 Da
Monoisotopic Mass300.1 Da
Topological Polar Surface Area57.900 Ų
Heavy Atom Count22
Formal Charge0
Complexity479.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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