(±)-Vasicine - ≥99% , CAS No.6159-56-4

Name: (±)-Vasicine - ≥99% , CAS No.6159-56-4
SKU: V649629
Availability: InStock

CAS: 6159-56-4 Cat. No.: V649629 Fórmula: C₁₁H₁₂N₂O Peso molecular: 188.23 PubChem CID: 72610

COA

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(±)-Vasicine - ≥99% CAS No(6159-56-4) by Aladdin Scientific

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Disponible para pedir

GRADE & PURITY ≥99%

Synonyms

Storage

Store at 2-8°C,Protected from light,Desiccated

Shipped In

Wet ice

Descripción general Specifications Nombres e identificadores Documentation Advanced Data Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Calculadoras de soluciones Reseñas

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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Protected from light,Desiccated Ships Wet ice 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

(±)-Vasicine is the racemate of Vasicine. Vasicine (Peganine) significantly inhibits H + -K + -ATPase activity in vitro with an IC 50 of 73.47 μg/mL. Anti-ulcer activity. Vasicine shows significant anti-secretory, antioxidant and cytoprotective effect.

In Vitro

Vasicine (Peganine) exhibits strong antioxidant activity in the DPPH inhibition assay with an IC 50 value of 71.97±3.79 μg/mL. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

Specifications

Sinónimos

Especificaciones y pureza

≥99%

Mecanismos bioquímicos y fisiológicos

(±)-Vasicine is the racemate of Vasicine. Vasicine (Peganine) significantly inhibits H + -K + -ATPase activityxa0in vitroxa0with an IC 50 of 73.47xa0μg/mL. Anti-ulcer activity. Vasicine shows significant anti-secretory, antioxidant andxa0cytoprotectivexa0

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C,Protected from light,Desiccated

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Tipo de acción

INHIBITOR

Pureza

≥99%

Nombres e identificadores

Sonrisas canónicas	C1CN2CC3=CC=CC=C3N=C2C1O
IUPAC Name	1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-3-ol
InChIKey	YIICVSCAKJMMDJ-UHFFFAOYSA-N
INCHI	1S/C11H12N2O/c14-10-5-6-13-7-8-3-1-2-4-9(8)12-11(10)13/h1-4,10,14H,5-7H2
Isómeros SMILES	C1CN2CC3=CC=CC=C3N=C2C1O
PubChem CID	72610
Peso molecular	188.23

Documentation

📋 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.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Clase Diazanaphthalenes
    - Subclass Benzodiazines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Clase	Diazanaphthalenes
Subclass	Benzodiazines
Intermediate Tree Nodes	Not available
Direct Parent	Quinazolines
Alternative Parents	N-alkylpyrrolidines Imidolactams Benzenoids Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Carboxamidines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Quinazoline - N-alkylpyrrolidine - Benzenoid - Imidolactam - Pyrrolidine - Secondary alcohol - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Amidine - Carboxylic acid amidine - Alcohol - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Descripción	This compound belongs to the class of organic compounds known as quinazolines. These are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.
External Descriptors	Not available
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

Estructura 3D

Objetivos asociados (humanos)

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

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

BCHE Tclin Butyrylcholinesterase (7174 Activities)

Discover Target: BCHE

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

A498 (42825 Activities)

Solubilidad	DMSO : 16.67 mg/mL (88.56 mM; Need ultrasonic)
Peso molecular	188.230 g/mol
XLogP3	0.400
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	188.095 Da
Monoisotopic Mass	188.095 Da
Topological Polar Surface Area	35.800 Å²
Heavy Atom Count	14
Formal Charge	0
Complexity	264.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

(±)​-​Vasicine - ≥99% , CAS No.6159-56-4