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Nuclear Fast Red Staining Solution - BioReagent, Biological Stain, for microscopy, 0.1%, high purity , CAS No.6409-77-4
Basic Description
Synonyms
Nuclear Fast Red | Kernechtrot | Calcium Red
Specifications & Purity
BioReagent, Biological Stain, for microscopy, 0.1%
Stability And Storage
Store at room temperature long term (12 months). Store in the dark.
Storage Temp
Protected from light,Room temperature
Shipped In
Normal
Grade
Biological Stain, BioReagent, for microscopy
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Anthracenes
Subclass
Anthraquinones
Intermediate Tree Nodes
Not available
Direct Parent
Hydroxyanthraquinones
Alternative Parents
Arylsulfonic acids and derivatives Aryl ketones Vinylogous amides Vinylogous acids Sulfonyls Organosulfonic acids Primary amines Organopnictogen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Hydroxyanthraquinone - Arylsulfonic acid or derivatives - Aryl ketone - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Vinylogous amide - Vinylogous acid - Ketone - Organic alkali metal salt - Organic sodium salt - Amine - Hydrocarbon derivative - Organic oxide - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organic salt - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as hydroxyanthraquinones. These are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.
External Descriptors
Not available
Data sources
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.
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
sodium;4-amino-1,3-dihydroxy-9,10-dioxoanthracene-2-sulfonate
INCHI
InChI=1S/C14H9NO7S.Na/c15-9-7-8(12(18)14(13(9)19)23(20,21)22)11(17)6-4-2-1-3-5(6)10(7)16;/h1-4,18-19H,15H2,(H,20,21,22);/q;+1/p-1
InChIKey
IFSXZLJQEKGQAF-UHFFFAOYSA-M
Smiles
C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C(=C3N)O)S(=O)(=O)[O-])O.[Na+]
Isomeric SMILES
C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C(=C3N)O)S(=O)(=O)[O-])O.[Na+]
WGK Germany
1
Molecular Weight
357.28
Reaxy-Rn
20093893
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=20093893&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
light-sensitive
Melt Point(°C)
300°C
Molecular Weight
357.270 g/mol
XLogP3
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
8
Rotatable Bond Count
1
Exact Mass
356.992 Da
Monoisotopic Mass
356.992 Da
Topological Polar Surface Area
166.000 Ų
Heavy Atom Count
24
Formal Charge
0
Complexity
634.000
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
2
Citations of This Product
1.
Hongxia Xiu, Yajie Liu, Huihui Yang, Haibin Ren, Bowen Luo, Zhipeng Wang, Hong Shao, Fengzhong Wang, Jingjian Zhang, Yutang Wang.
(2022)
Identification of novel umami molecules via QSAR models and molecular docking. Food & Function,
13
(14):
(7529-7539).
2.
Hui-Hui Xiao, Quan-Gui Gao, Ming-Xian Ho, Yan Zhang, Ka-Chun Wong, Yi Dai, Xin-Sheng Yao, Man-Sau Wong.
(2015)
An 8-O-4′ norlignan exerts oestrogen-like actions in osteoblastic cells via rapid nongenomic ER signaling pathway. JOURNAL OF ETHNOPHARMACOLOGY,
170
(39).
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2 Citations