Paprotrain - ≥98% , CAS No.57046-73-8

CAS: 57046-73-8 Cat. No.: P276275 Formula: C16H11N3 Peso molecolare: 245.28 Numero EC: 988-671-4 PubChem CID: 12248889
Disponibile su ordine
GRADE & PURITY ≥98%
Synonyms
(Z)-2-(1H-Indol-3-yl)-3-pyridin-3-ylprop-2-enenitrile
Storage
Protected from light,Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
Size
Germania (EU)
USA*
Price
Qty
10mg
P276275-10mg
2 Disponibile
102,31€
25mg
P276275-25mg
2 Disponibile
156,11€
50mg
P276275-50mg
2 Disponibile
249,82€
100mg
P276275-100mg
2 Disponibile
390,40€
200mg
P276275-200mg
2 Disponibile
629,89€
500mg
P276275-500mg
2 Disponibile
1.416,93€
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Store at -20°C,Desiccated Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinonimi
(Z)-2-(1H-Indol-3-yl)-3-pyridin-3-ylprop-2-enenitrile
Specifiche e purezza
≥98%
Meccanismi biochimici e fisiologici
Selective cell-permeable MKLP-2 inhibitor. Reversible ATP-noncompetitive ATPase inhibitor (IC 50 values are 1.35 and 0.83 µM for basal and microtubule-stimulated activity respectively). Inhibits Aurora B. Induces cell cycle arrest at early metaphase I.
Condizioni di conservazione di stoccaggio
Protected from light,Store at -20°C,Desiccated
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Tipo di azione
INHIBITOR
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purezza
≥98%
Nomi e identificatori
Pubchem Sid504767014
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504767014
Sorrisi canoniciC1=CC=C2C(=C1)C(=CN2)C(=CC3=CN=CC=C3)C#N
IUPAC Name(Z)-2-(1H-indol-3-yl)-3-pyridin-3-ylprop-2-enenitrile
InChIKeyYMYYQRZCCKBFBE-MDWZMJQESA-N
INCHI1S/C16H11N3/c17-9-13(8-12-4-3-7-18-10-12)15-11-19-16-6-2-1-5-14(15)16/h1-8,10-11,19H/b13-8+
Isomeri SMILES C1=CC=C2C(=C1)C(=CN2)/C(=C/C3=CN=CC=C3)/C#N
PubChem CID 12248889
Peso molecolare 245.28

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseIndoles and derivatives
SubclassIndoles
Intermediate Tree Nodes Not available
Direct ParentIndoles
Alternative Parents Substituted pyrroles  Pyridines and derivatives  Benzenoids  Heteroaromatic compounds  Nitriles  Azacyclic compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indole - Benzenoid - Substituted pyrrole - Pyridine - Heteroaromatic compound - Pyrrole - Azacycle - Nitrile - Carbonitrile - Organic nitrogen compound - Cyanide - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
KIF20A Tchem Kinesin-like protein KIF20A (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
DYRK1A Tchem Dual-specificity tyrosine-phosphorylation regulated kinase 1A (6484 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CLK1 Tchem Dual specificty protein kinase CLK1 (2189 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KB (17409 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK5 Tchem Cyclin-dependent kinase 5/CDK5 activator 1 (3697 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KIF20A Tchem Kinesin-like protein KIF20A (148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSK3A Tclin Glycogen synthase kinase-3 (736 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
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.

7 results found

Lot NumberCertificate TypeDataOggetto
E2619117Certificate of AnalysisMay 29, 2026 P276275
C23021118Certificate of AnalysisSep 19, 2024 P276275
C23021123Certificate of AnalysisSep 19, 2024 P276275
C23021124Certificate of AnalysisSep 19, 2024 P276275
C23021128Certificate of AnalysisSep 19, 2024 P276275
C23021220Certificate of AnalysisSep 19, 2024 P276275
C23021234Certificate of AnalysisSep 19, 2024 P276275
Proprietà chimiche e fisiche
SolubilitàSoluble in DMSO to 5 mM
Sensibilitàlight sensitive
Peso molecolare245.280 g/mol
XLogP32.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass245.095 Da
Monoisotopic Mass245.095 Da
Topological Polar Surface Area52.500 Ų
Heavy Atom Count19
Formal Charge0
Complexity392.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Citations of This Product
Riferimenti
1. Huanhuan Hu, Pengbo Wang, Zhihong Kong, Yibo Yang, Siyun Liu, Guanjie Li, Chuhan Wang, Jiaqi Jiang, Qifang He, Xiangxiang Cao, Qiaohui Zhao, Huigen Feng, Guojie Ji.  (2026)  KIF20A drives epithelial cell proliferation and migration in gastric adenocarcinoma, facilitating macrophage M2 polarization and subsequent immune evasion.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41713545] [10.1016/j.ijbiomac.2026.150982]
Calcolatori di soluzioni
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