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Merck
CN

91625

Vasicinone

analytical standard

Synonym(s):

(3S)-2,3-Dihydro-3-hydroxypyrrolo[2,1-b]quinazolin-9(1H)-one

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About This Item

Empirical Formula (Hill Notation):
C11H10N2O2
CAS Number:
Molecular Weight:
202.21
UNSPSC Code:
12352200
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
7463808
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grade

analytical standard

Quality Level

assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

format

neat

SMILES string

O=C1N2C([C@@H](O)CC2)=NC3=CC=CC=C31

InChI

1S/C11H10N2O2/c14-9-5-6-13-10(9)12-8-4-2-1-3-7(8)11(13)15/h1-4,9,14H,5-6H2/t9-/m0/s1

InChI key

SDIVYZXRQHWCKF-VIFPVBQESA-N

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.


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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

涉药品监管产品

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Faten Y Ibrahim et al.
Foods (Basel, Switzerland), 8(4) (2019-04-26)
Green synthesis of metal nanoparticles using plant extracts offers a safe and attractive alternate to the chemical methods. The present work aims at preparing metal nanoparticles of rhus (Rhus coriaria L.) and safflower (Carthamus tinctorius L.) extracts using Fe2+, Cu2+
Tapan Dey et al.
Biomolecules & therapeutics, 26(4), 409-416 (2018-01-10)
Vasicinone, a quinazoline alkaloid from Adhatoda vasica Nees. is well known for its bronchodilator activity. However its anti-proliferative activities is yet to be elucidated. Here-in we investigated the anti-proliferative effect of vasicinone and its underlying mechanism against A549 lung carcinoma
Holger Jahr et al.
International journal of molecular sciences, 20(7) (2019-04-10)
Culturing articular chondrocytes under physiological oxygen tension exerts positive effects on their extracellular matrix synthesis. The underlying molecular mechanisms which enhance the chondrocytic phenotype are, however, still insufficiently elucidated. The TGF-β superfamily of growth factors, and the prototypic TGF-β isoforms



Global Trade Item Number

SKUGTIN
91625-10MG04061833263563