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Preuve documentaire

Cité dans 9 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

When bound to DNA, it emits green fluorescence (Em=525 nm) and when bound to RNA, it emits red fluorescence (Em=~650 nm).
A fluorescent nucleic acid binding dye which interacts with both DNA and RNA.

Spécifications

Synonymes

Spécifications et pureté

≥75%

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥75%

Noms et identifiants

Pubchem Sid

488183564

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488183564

Sourires canoniques

CN(C)C1=CC2=C(C=C1)C=C3C=CC(=CC3=N2)N(C)C

IUPAC Name

3-N,3-N,6-N,6-N-tetramethylacridine-3,6-diamine

InChIKey

DPKHZNPWBDQZCN-UHFFFAOYSA-N

INCHI

1S/C17H19N3/c1-19(2)14-7-5-12-9-13-6-8-15(20(3)4)11-17(13)18-16(12)10-14/h5-11H,1-4H3

Isomères SMILES

CN(C)C1=CC2=C(C=C1)C=C3C=CC(=CC3=N2)N(C)C

WGK Allemagne

RTECS

AR7600000

Poids moléculaire

265.35

Reaxy-Rn

20916

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=20916&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

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Résumé de référence rapide des spécifications et applications du produit.

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Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Classe Quinolines and derivatives
    - Subclass Benzoquinolines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Classe	Quinolines and derivatives
Subclass	Benzoquinolines
Intermediate Tree Nodes	Not available
Direct Parent	Acridines
Alternative Parents	Aminoquinolines and derivatives Dialkylarylamines Pyridines and derivatives Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Acridine - Aminoquinoline - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Benzenoid - Pyridine - Heteroaromatic compound - Tertiary amine - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as acridines. These are organic compounds containing the acridine moiety, a linear tricyclic heterocycle which consists of two benzene rings joined by a pyridine ring.
External Descriptors	aminoacridines - tertiary amino compound - aromatic amine
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

APP Tclin Amyloid-beta A4 protein (1 Activities)

Discover Target: APP

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

APP Tclin Amyloid-beta A4 protein (8510 Activities)

Discover Target: APP

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TERT Tchem Telomerase reverse transcriptase (2428 Activities)

Discover Target: TERT

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A498 (42825 Activities)

Lot Number	Certificate Type	Date	Article
I2418141	Certificate of Analysis	Sep 04, 2024	A121748
I2418140	Certificate of Analysis	Sep 04, 2024	A121748
I2418139	Certificate of Analysis	Sep 04, 2024	A121748
H2422065	Certificate of Analysis	Aug 13, 2024	A121748
I2402492	Certificate of Analysis	Jun 06, 2023	A121748
K2324092	Certificate of Analysis	Jun 06, 2023	A121748
F2313119	Certificate of Analysis	Jun 06, 2023	A121748
F2313116	Certificate of Analysis	Jun 06, 2023	A121748
F2313112	Certificate of Analysis	Jun 06, 2023	A121748
D2629013	Certificate of Analysis	Jun 06, 2023	A121748
C2302208	Certificate of Analysis	Mar 15, 2023	A121748
C2302207	Certificate of Analysis	Oct 28, 2022	A121748
D2315307	Certificate of Analysis	Oct 28, 2022	A121748
D2310195	Certificate of Analysis	Oct 28, 2022	A121748
K2222247	Certificate of Analysis	Oct 28, 2022	A121748
K2222248	Certificate of Analysis	Oct 28, 2022	A121748
K2222322	Certificate of Analysis	Oct 28, 2022	A121748
J2210149	Certificate of Analysis	Sep 20, 2022	A121748

Point de fusion (°C)	165°C(dec.)(lit.)
Poids moléculaire	265.350 g/mol
XLogP3	3.400
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	2
Exact Mass	265.158 Da
Monoisotopic Mass	265.158 Da
Topological Polar Surface Area	19.400 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	298.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Acridine Orange base - ≥75% , CAS No.494-38-2

Stockage & expédition

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Preuve documentaire

Vue d’ensemble

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Documentation

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