152102
Isocarbostyril
98%
Sinónimos:
1(2H)-Isoquinolinone, 1-Hydroxyisoquinoline, 1-Isoquinolinol
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About This Item
Productos recomendados
Quality Level
assay
98%
form
solid
mp
211-214 °C (lit.)
SMILES string
Oc1nccc2ccccc12.O=C3NC=Cc4ccccc34
InChI
1S/C9H7NO/c11-9-8-4-2-1-3-7(8)5-6-10-9/h1-6H,(H,10,11)
InChI key
VDBNYAPERZTOOF-UHFFFAOYSA-N
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Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Open biology, 9(4), 190041-190041 (2019-04-18)
ADP-ribosylation (ADPr) is a reversible post-translational modification of proteins, which controls major cellular and biological processes, including DNA damage repair, cell proliferation and differentiation, metabolism, stress and immune responses. In order to maintain the cellular homeostasis, diverse ADP-ribosyl transferases and
Nucleic acids research, 28(15), 2911-2914 (2000-07-25)
Several unnatural, predominantly hydrophobic nucleobases that pack efficiently in duplex DNA without hydrogen bonding functionalities are reported to circumvent the hydrogen bonding-based specificity, both during oligonucleotide hybridization and enzymatic DNA synthesis. The reported nucleoside analogs are efficient 'universal bases' for
Canadian journal of microbiology, 40(7), 561-566 (1994-07-01)
To facilitate the cloning of DNA encoding isoquinoline degradation an assay was developed that allowed the rapid visual scoring of the isoquinoline degradation phenotype of single colonies. Transposon mutagenesis of one of the isolates. Comamonas acidovorans IQ3, was performed using
Carbohydrate polymers, 209, 338-349 (2019-02-09)
The effect of wheat straw arabinoxylan (AX) and β-glucan stearic acid ester (SABG) composite coating on the quality and storage life of apple (Royal Delicious) was studied at 22 °C (±2) with relative humidity of 65% and 85% for 60 days.
Nucleosides, nucleotides & nucleic acids, 20(8), 1533-1553 (2001-09-14)
A group of unnatural 1-(2-deoxy-beta-D-ribofuranosyl)isocarbostyrils having a variety of C-7 substituents [H, 4,7-(NO2)2, I, CF3, CN, (E)-CH=CH-I, -C triple bond CH, -C triple bond C-I, -C triple bond C-Br, -C=C-Me], designed as nucleoside mimics, were synthesized for evaluation as anticancer
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