UCM 608 - ≥98%(HPLC) , CAS No.151889-03-1

CAS: 151889-03-1 Cat. No.: P288352 Summenformel: C19H20N2O2 Molekulargewicht: 308.38 PubChem CID: 4018512
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QUALITÄT & REINHEIT ≥98%(HPLC)
Synonyms
UCM608;UCM-608 | CHEBI:107661 | Q27185983 | UCM 608 | N-[2-(5-METHOXY-2-PHENYLINDOL-3-YL)ETHYL]ACETAMIDE | AM20030035 | PDSP2_001778 | SR-01000597657 | NCGC00024727-02 | HMS3675O18 | PDSP1_001796 | HY-101074 | Tocris-0680 | BRD-K41869275-001-01-0 | Melato
Storage
Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
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Preis
Menge
5mg
P288352-5mg
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2 Auf Lager
156,11€
10mg
P288352-10mg
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3 Auf Lager
249,82€
25mg
P288352-25mg
—
2 Auf Lager
499,73€
50mg
P288352-50mg
—
2 Auf Lager
812,12€
100mg
P288352-100mg
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2 Auf Lager
1.296,32€
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Warum diese Qualität

≥98%(HPLC) für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

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

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Qualitätsdokumente

SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

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

Übersicht

Product Describtion:

UCM 608 is a high affinity melatonin (MT) membrane receptor agonist. The pKi values for MT1 and MT2 are 10.7 and 10.4.

Spezifikationen

Synonyme
UCM608;UCM-608 | CHEBI:107661 | Q27185983 | UCM 608 | N-[2-(5-METHOXY-2-PHENYLINDOL-3-YL)ETHYL]ACETAMIDE | AM20030035 | PDSP2_001778 | SR-01000597657 | NCGC00024727-02 | HMS3675O18 | PDSP1_001796 | HY-101074 | Tocris-0680 | BRD-K41869275-001-01-0 | Melato
Spezifikationen & Reinheit
≥98%(HPLC)
Biochemische und physiologische Mechanismen
Highly potent melatonin agonist; displays higher affinity and greater potency than melatonin itself. The EC50values for G protein activation in MT1and MT2-transfected cells are 65 and 58 pM respectively.
Storage
Store at -20°C,Desiccated
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥98%(HPLC)
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488194651
Kanonisches Lächeln
CC(=O)NCCC1=C(NC2=C1C=C(C=C2)OC)C3=CC=CC=C3
IUPAC Name
N-[2-(5-methoxy-2-phenyl-1H-indol-3-yl)ethyl]acetamide
InChIKey
OFCLARYYBGKCHN-UHFFFAOYSA-N
INCHI
1S/C19H20N2O2/c1-13(22)20-11-10-16-17-12-15(23-2)8-9-18(17)21-19(16)14-6-4-3-5-7-14/h3-9,12,21H,10-11H2,1-2H3,(H,20,22)
Isomere SMILES
CC(=O)NCCC1=C(NC2=C1C=C(C=C2)OC)C3=CC=CC=C3
PubChem CID
4018512
Molekulargewicht
308.38

Dokumentation

📋 Sicherheitsdatenblatt (SDS)

Umfassendes Dokument zu Gefahren, Handhabung, Lagerung und Einhaltung regulatorischer Vorschriften.

<<<<<<< HEAD SDS herunterladen → ======= SDS herunterladen → >>>>>>> release248-p3

✅ Analysezertifikat (COA)

Chargenspezifische Qualitätsdaten. Geben Sie Ihre Chargennummer ein, um das genaue COA abzurufen.

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📊 Datenblatt

Kurzübersicht über Produktspezifikationen und Anwendungen.

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🔬 Spezifikationsblatt

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
KlasseIndoles and derivatives
SubclassIndoles
Intermediate Tree Nodes Not available
Direct Parent2-phenylindoles
Alternative Parents Phenylpyrroles  N-acetyl-2-arylethylamines  3-alkylindoles  Anisoles  Alkyl aryl ethers  Benzene and substituted derivatives  Heteroaromatic compounds  Secondary carboxylic acid amides  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 2-phenylindole - 2-phenylpyrrole - N-acetyl-2-arylethylamine - 3-alkylindole - Anisole - Alkyl aryl ether - Monocyclic benzene moiety - Substituted pyrrole - Benzenoid - Pyrrole - Heteroaromatic compound - Acetamide - Secondary carboxylic acid amide - Carboxamide group - Ether - Carboxylic acid derivative - Azacycle - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as 2-phenylindoles. These are indoles substituted at the 2-position with a phenyl group.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
MTNR1A Tclin Melatonin receptor 1A (2519 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MTNR1A Tclin Melatonin receptor (989 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Melatonin receptor 1B (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cruzipain (33337 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Impa1 Inositol monophosphatase 1 (16203 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:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot NumberCertificate TypeDatumArtikel
D2311688D2311688Certificate of AnalysisJan 20, 2026 P288352
D2311696D2311696Certificate of AnalysisJan 20, 2026 P288352
D2311697D2311697Certificate of AnalysisJan 20, 2026 P288352
D2311699D2311699Certificate of AnalysisJan 20, 2026 P288352
D2311707D2311707Certificate of AnalysisJan 20, 2026 P288352
D2311710D2311710Certificate of AnalysisJan 20, 2026 P288352
D2311711D2311711Certificate of AnalysisJan 20, 2026 P288352
D2311726D2311726Certificate of AnalysisJan 20, 2026 P288352
D2311735D2311735Certificate of AnalysisJan 20, 2026 P288352
D2311736D2311736Certificate of AnalysisJan 20, 2026 P288352
Chemische und physikalische Eigenschaften
LöslichkeitSolvent:ethanol, Max Conc. mg/mL: 30.84, Max Conc. mM: 100; Solvent:DMSO, Max Conc. mg/mL: 30.84, Max Conc. mM: 100
Molekulargewicht308.400 g/mol
XLogP33.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count5
Exact Mass308.152 Da
Monoisotopic Mass308.152 Da
Topological Polar Surface Area54.100 Ų
Heavy Atom Count23
Formal Charge0
Complexity395.000
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
Lösungsrechner
Bewertungen

Kundenbewertungen

Häufig gestellte Fragen

What is the purity of this product, and how is it determined?
This product is supplied at ≥98% purity, determined by HPLC. Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at ?20 °C, desiccated. Keep the container tightly closed with desiccant — the material is moisture-sensitive.
How is this product shipped?
This product ships in an insulated container with ice pads. Unpack on arrival and transfer it to the storage condition stated above.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 151889-03-1, the molecular formula is C??H??N?O?, and the molecular weight is 308.38 g/mol. InChIKey OFCLARYYBGKCHN-UHFFFAOYSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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