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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H15NO8
Molecular Weight 301.2494
Optical Activity ( - )
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of O-NITROPHENYL .BETA.-D-GALACTOPYRANOSIDE

SMILES

OC[C@H]1O[C@@H](OC2=CC=CC=C2[N+]([O-])=O)[C@H](O)[C@@H](O)[C@H]1O

InChI

InChIKey=KUWPCJHYPSUOFW-YBXAARCKSA-N
InChI=1S/C12H15NO8/c14-5-8-9(15)10(16)11(17)12(21-8)20-7-4-2-1-3-6(7)13(18)19/h1-4,8-12,14-17H,5H2/t8-,9+,10+,11-,12-/m1/s1

HIDE SMILES / InChI

Molecular Formula C12H15NO8
Molecular Weight 301.2494
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Beta-galactosidase (Lactobacillus helveticus)
Target ID: Beta-galactosidase (Aspergillus oryzae)
PubMed

PubMed

TitleDatePubMed
Toxic potential of synthesized graphene zinc oxide nanocomposite in the third instar larvae of transgenic Drosophila melanogaster (hsp70-lacZ)Bg9.
2014
Identification and characterization of an unusual glycosyltransferase-like enzyme with β-galactosidase activity from a soil metagenomic library.
2014 Apr 10
High level production of β-galactosidase exhibiting excellent milk-lactose degradation ability from Aspergillus oryzae by codon and fermentation optimization.
2014 Mar
Improving Properties of a Novel β-Galactosidase from Lactobacillus plantarum by Covalent Immobilization.
2015 Apr 30
Effect of the pH in the formation of β-galactosidase microparticles produced by a spray-drying process.
2015 Jul
Human milk and mucosal lacto- and galacto-N-biose synthesis by transgalactosylation and their prebiotic potential in Lactobacillus species.
2017 Jan
β-Galactosidase from Lactobacillus helveticus DSM 20075: Biochemical Characterization and Recombinant Expression for Applications in Dairy Industry.
2019 Feb 22
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:35:44 GMT 2023
Edited
by admin
on Sat Dec 16 17:35:44 GMT 2023
Record UNII
8RFX6AT9WP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
O-NITROPHENYL .BETA.-D-GALACTOPYRANOSIDE
Common Name English
ORTHO-NITROPHENYL-.BETA.-GALACTOSIDE
Common Name English
.BETA.-D-GALACTOPYRANOSIDE, 2-NITROPHENYL
Systematic Name English
GALACTOPYRANOSIDE, O-NITROPHENYL, .BETA.-D-
Common Name English
1-O-(O-NITROPHENYL)-BETA-D-GALACTOPYRANOSE
Systematic Name English
ONPG
Common Name English
2-NITROPHENYL .BETA.-D-GALACTOPYRANOSIDE
Systematic Name English
2-NITROPHENYL .BETA.-D-GALACTOSIDE
Systematic Name English
O-NPG
Common Name English
O-NITROPHENOL .BETA.-D-GALACTOPYRANOSIDE
Common Name English
NSC-83631
Code English
O-NITROPHENYL .BETA.-D-GALACTOSIDE
Common Name English
O-NITROPHENYL .BETA.-GALACTOSIDE
Common Name English
O-NITROPHENYL-.BETA.-GALACTOPYRANOSIDE
Common Name English
Code System Code Type Description
CAS
28347-45-7
Created by admin on Sat Dec 16 17:35:44 GMT 2023 , Edited by admin on Sat Dec 16 17:35:44 GMT 2023
SUPERSEDED
CAS
369-07-3
Created by admin on Sat Dec 16 17:35:44 GMT 2023 , Edited by admin on Sat Dec 16 17:35:44 GMT 2023
PRIMARY
FDA UNII
8RFX6AT9WP
Created by admin on Sat Dec 16 17:35:44 GMT 2023 , Edited by admin on Sat Dec 16 17:35:44 GMT 2023
PRIMARY
WIKIPEDIA
ortho-Nitrophenyl-β-galactoside
Created by admin on Sat Dec 16 17:35:44 GMT 2023 , Edited by admin on Sat Dec 16 17:35:44 GMT 2023
PRIMARY
NSC
83631
Created by admin on Sat Dec 16 17:35:44 GMT 2023 , Edited by admin on Sat Dec 16 17:35:44 GMT 2023
PRIMARY
DRUG BANK
DB01920
Created by admin on Sat Dec 16 17:35:44 GMT 2023 , Edited by admin on Sat Dec 16 17:35:44 GMT 2023
PRIMARY
EPA CompTox
DTXSID10861907
Created by admin on Sat Dec 16 17:35:44 GMT 2023 , Edited by admin on Sat Dec 16 17:35:44 GMT 2023
PRIMARY
CAS
103737-63-9
Created by admin on Sat Dec 16 17:35:44 GMT 2023 , Edited by admin on Sat Dec 16 17:35:44 GMT 2023
NON-SPECIFIC SUBSTITUTION
PUBCHEM
96647
Created by admin on Sat Dec 16 17:35:44 GMT 2023 , Edited by admin on Sat Dec 16 17:35:44 GMT 2023
PRIMARY