HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HCID 4879Erstellt: 4. November 2026
4-Amino-1-phenylpyrazolo(3,4-d)pyrimidine
Inetetamab · PP3 · Amino d · NSC 1401 · PP-3 · PP 3 · PP 3, 10 mM in DMSO · PP3 ISO 9001:2015 REACH
https://huagongshe.com/de/chemical/4879
Identifikatoren & physikalische Daten
| CAS No. | 5334-30-5 |
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| Summenformel | C11H9N5 |
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| Durchschnittliche Molmasse | 211,22 g/mol |
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| Monoisotopische Masse | 211,08579531 g/mol |
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| SMILES | Nc1ncnc2c1cnn2-c1ccccc1 |
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| InChIKey | KKDPIZPUTYIBFX-UHFFFAOYSA-N |
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| PubChem CID | 4879 |
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| ChEMBL | CHEMBL65063 |
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| ChEBI | CHEBI:92303 |
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| EC No. | 808-056-5 |
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| DTXSID | DTXSID20274448 |
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Chemische & physikalische Eigenschaften
| XLogP | 1,5 |
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| Polarare Oberfläche (TPSA) | 69,6 |
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| H-Brücken-Donoren | 1 |
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| H-Brücken-Akzeptoren | 4 |
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| Frei drehbare Bindungen | 1 |
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| Schwere Atome | 16 |
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| Formalladung | 0 |
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| Komplexität | 241 |
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| Schmelzpunkt | 214-217 °C |
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| Siedepunkt | 363.952±35.00 °C(Press: 760.00 Torr)(predicted) |
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| Dichte | 1.448±0.14 g/cm3(Temp: 25 °CPress: 760 Torr)(predicted) |
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| Lagerbedingungen | -20°C |
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| Löslichkeit | DMF, DMSO, Hot methanol |
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| pKa (Säurekonstante) | 3.89 |
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| Aggregatzustand | Off-white solid |
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| Farbe | Whit to Off-White |
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| BRN | 198460 |
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| CAS Datenbank | 5334-30-5(CAS DataBase Reference) |
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Sicherheit & Vorschriften
| GHS-Einstufung | WarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364 (click each P-code to see the statement)The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory. |
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| Hazard Classes and Categories | Skin Irrit. 2 (100%) |
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| Zollcode | 29335995 |
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| R-Sätze (R) | 36/37/38-22 |
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| Gefahrensymbole | Xn,Xi |
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| hazard_note | Irritant |
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| Sicherheitshinweise (S) | 36/37/39-26 |
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Anwendungen & Verwendung
Verwenden
The Src family of non-receptor tyrosine kinases regulate cell adhesion, growth, and differentiation through activation of multiple intracellular signaling pathways. Normally inactive, Src kinases are transiently activated during mitosis and constitutively activated by abnormal mutations. Several small molecule inhibitors of this signaling pathway have been developed as a therapeuptic strategy to abate abnormal Src kinase activity. PP3 is an inactive analog of the Src tyrosine kinase inhibitors PP1 and PP2 . At concentrations as high as 10 μM, it does not prevent proliferation mediated by a stem cell factor/mast cell growth factor in hematopoietic and cancer cell lines.[Cayman Chemical]