YM201636 - ≥96% , CAS No.371942-69-7

CAS: 371942-69-7 Cat. No.: Y126759 Summenformel: C25H21N7O3 Molekulargewicht: 467.48 PubChem CID: 9956222
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QUALITÄT & REINHEIT ≥96%
Synonyms
AKOS027250783 | HY-13228 | SW218129-2 | 6-Amino-N-[3-[4-(4-morpholinyl)pyrido[3',2':4,5]furo[3,2-d]pyrimidin-2-yl]phenyl]-3-pyridinecarboxamide;YM-201636 | AMY23718 | FT-0756177 | (R)-Alpha-(2-pyrrolidinyl)benzhydryl alcohol | 6-Amino-N-{3-[4-(morpholin-4
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Menge
5mg
Y126759-5mg
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6 Auf Lager
136,15€
10mg
Y126759-10mg
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6 Auf Lager
217,72€
25mg
Y126759-25mg
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5 Auf Lager
407,75€
50mg
Y126759-50mg
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5 Auf Lager
652,45€
100mg
Y126759-100mg
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5 Auf Lager
1.223,43€
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Warum diese Qualität

≥96% für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Store at -20°C 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.

Spezifikationen

Synonyme
AKOS027250783 | HY-13228 | SW218129-2 | 6-Amino-N-[3-[4-(4-morpholinyl)pyrido[3',2':4,5]furo[3,2-d]pyrimidin-2-yl]phenyl]-3-pyridinecarboxamide;YM-201636 | AMY23718 | FT-0756177 | (R)-Alpha-(2-pyrrolidinyl)benzhydryl alcohol | 6-Amino-N-{3-[4-(morpholin-4
Spezifikationen & Reinheit
≥96%
Biochemische und physiologische Mechanismen
YM-201636 is a cell-permeable and selective inhibitor of PIKfyve (IC50 = 33 nM).PIKfyve is a phosphoinositide kinase (PIK) that contains a FYVE-type zinc finger domain. YM-201636 is a cell-permeable and selective inhibitor of PIKfyve (IC50 = 33 nM). binds
Storage
Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥96%
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488196470
Kanonisches Lächeln
C1COCCN1C2=NC(=NC3=C2OC4=C3C=CC=N4)C5=CC(=CC=C5)NC(=O)C6=CN=C(C=C6)N
IUPAC Name
6-amino-N-[3-(6-morpholin-4-yl-8-oxa-3,5,10-triazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3,5,10,12-hexaen-4-yl)phenyl]pyridine-3-carboxamide
InChIKey
YBPIBGNBHHGLEB-UHFFFAOYSA-N
INCHI
1S/C25H21N7O3/c26-19-7-6-16(14-28-19)24(33)29-17-4-1-3-15(13-17)22-30-20-18-5-2-8-27-25(18)35-21(20)23(31-22)32-9-11-34-12-10-32/h1-8,13-14H,9-12H2,(H2,26,28)(H,29,33)
Isomere SMILES
C1COCCN1C2=NC(=NC3=C2OC4=C3C=CC=N4)C5=CC(=CC=C5)NC(=O)C6=CN=C(C=C6)N
PubChem CID
9956222
Molekulargewicht
467.48

Dokumentation

📋 Sicherheitsdatenblatt (SDS)

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

✅ Analysezertifikat (COA)

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
KlasseBenzene and substituted derivatives
SubclassAnilides
Intermediate Tree Nodes Not available
Direct ParentAromatic anilides
Alternative Parents Nicotinamides  Furopyridines  Dialkylarylamines  Aminopyridines and derivatives  Aminopyrimidines and derivatives  Morpholines  Imidolactams  Heteroaromatic compounds  Furans  Secondary carboxylic acid amides  Amino acids and derivatives  Oxacyclic compounds  Azacyclic compounds  Dialkyl ethers  Hydrocarbon derivatives  Organic oxides  Organopnictogen compounds  Primary amines  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Aromatic anilide - Pyridinecarboxamide - Furopyridine - Pyridine carboxylic acid or derivatives - Nicotinamide - Dialkylarylamine - Aminopyridine - Aminopyrimidine - Pyridine - Pyrimidine - Imidolactam - Oxazinane - Morpholine - Furan - Heteroaromatic compound - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Amine - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - Primary amine - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as aromatic anilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl group.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSK3B Tclin Glycogen synthase kinase-3 beta (11785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CSNK1D Tchem Casein kinase I delta (4546 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK2 Tchem Cyclin-dependent kinase 2 (9050 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIK3CB Tchem PI3-kinase p110-beta subunit (4044 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AURKA Tchem Serine/threonine-protein kinase Aurora-A (10240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U2OS (164939 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRD4 Tchem Bromodomain-containing protein 4 (13122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIKFYVE Tchem 1-phosphatidylinositol 3-phosphate 5-kinase (270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TRIM24 Tchem Transcription intermediary factor 1-alpha (2087 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRPF1 Tchem Peregrin (2217 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK-293T (167025 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fgfr3 Fibroblast growth factor receptor 3 (21 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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HT-22 (3261 Activities)
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SARS-CoV-2 (38078 Activities)
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Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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11 results found

Lot NumberCertificate TypeDatumArtikel
K2526102K2526102Certificate of AnalysisDec 10, 2025 Y126759
E2316808E2316808Certificate of AnalysisFeb 07, 2025 Y126759
E2316809E2316809Certificate of AnalysisFeb 07, 2025 Y126759
E2316810E2316810Certificate of AnalysisFeb 07, 2025 Y126759
E2316811E2316811Certificate of AnalysisFeb 07, 2025 Y126759
E2316812E2316812Certificate of AnalysisFeb 07, 2025 Y126759
E2316813E2316813Certificate of AnalysisFeb 07, 2025 Y126759
E2316815E2316815Certificate of AnalysisFeb 07, 2025 Y126759
E2316824E2316824Certificate of AnalysisFeb 07, 2025 Y126759
E2316825E2316825Certificate of AnalysisFeb 07, 2025 Y126759
E2316826E2316826Certificate of AnalysisFeb 07, 2025 Y126759
Chemische und physikalische Eigenschaften
LöslichkeitDMSO 35 mg/mL Water <1 mg/mL Ethanol <1 mg/mL
Molekulargewicht467.500 g/mol
XLogP32.500
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count9
Rotatable Bond Count4
Exact Mass467.171 Da
Monoisotopic Mass467.171 Da
Topological Polar Surface Area132.000 Ų
Heavy Atom Count35
Formal Charge0
Complexity738.000
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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