JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Small Molecules & Compound Libraries
Signaling Pathways
NF-κB
NF-κB
Adelmidrol - 98%, high purity , CAS No.1675-66-7

Skip to the end of the images gallery

Skip to the beginning of the images gallery

Adelmidrol - 98%, high purity , CAS No.1675-66-7

COA

Grade & Purity:

≥98%

Cas Number: 1675-66-7
Molecular Weight: 274.36
PubChem CID: 176874
PubChem SID: 488188500

In stock

Item Number

A413515

Grouped product items
SKU	Size	Availability	Price
A413515-25mg	25mg	6	$21.90
A413515-100mg	100mg	6	$70.90
A413515-250mg	250mg	4	$159.90
A413515-500mg	500mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$360.90
A413515-1g	1g	3	$575.90
A413515-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$2,448.90

View related series

Cell Cycle (2830) Cell Cycle/DNA Damage (2602) COX (258) Immunology/Inflammation (1929) Lipid metabolism (1912) NF-κB (747) PPAR (155) Vitamin D Related/Nuclear Receptor (907)

Basic Description

Synonyms	EX-A1239 \| 3-(Dibutylamino)-1-(1,3-dichlor-6-(trifluormethyl)-9-phenanthryl)propanol \| C73226 \| N1,N9-Bis(2-hydroxyethyl)nonanediamide \| SR-01000944279 \| BCP24910 \| AKOS028111150 \| AS-56183 \| Adelmidrol \| NSC27132 \| NSC-27132 \| 1BUC3685QU \| CCG-213729 \| A
Specifications & Purity	≥98%
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Product description： Adelmidrol exerts important anti-inflammatory effects that are partly dependent on PPARγ. Adelmidrol reduces NF-κB translocation, and COX-2 expression.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic nitrogen compounds
  - Class Organonitrogen compounds
    - Subclass Amines
      - Level5 Alkanolamines
        Level6 1,2-aminoalcohols
        Level7 N-acylethanolamines

Kingdom	Organic compounds
Superclass	Organic nitrogen compounds
Class	Organonitrogen compounds
Subclass	Amines
Intermediate Tree Nodes	Alkanolamines - 1,2-aminoalcohols
Direct Parent	N-acylethanolamines
Alternative Parents	N-acyl amines Secondary carboxylic acid amides Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	N-acylethanolamine - Fatty amide - N-acyl-amine - Fatty acyl - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Alcohol - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as n-acylethanolamines. These are compounds containing an N-acyethanolamine moiety, which is characterized by an acyl group is linked to the nitrogen atom of ethanolamine.
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

Product Properties

ALogP	-0.001
hba_count	2
HBD Count	4
Rotatable Bond	12

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488188500
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488188500
IUPAC Name	N,N'-bis(2-hydroxyethyl)nonanediamide
INCHI	InChI=1S/C13H26N2O4/c16-10-8-14-12(18)6-4-2-1-3-5-7-13(19)15-9-11-17/h16-17H,1-11H2,(H,14,18)(H,15,19)
InChIKey	PAHZPHDAJQIETD-UHFFFAOYSA-N
Smiles	C(CCCC(=O)NCCO)CCCC(=O)NCCO
Isomeric SMILES	C(CCCC(=O)NCCO)CCCC(=O)NCCO
Molecular Weight	274.36
Reaxy-Rn	1798605
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1798605&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

13 results found

Lot Number	Certificate Type	Date	Item
E2413105	Certificate of Analysis	Mar 26, 2024	A413515
E2413104	Certificate of Analysis	Mar 26, 2024	A413515
E2413106	Certificate of Analysis	Mar 26, 2024	A413515
E2413111	Certificate of Analysis	Mar 26, 2024	A413515
E2413112	Certificate of Analysis	Mar 26, 2024	A413515
D2318057	Certificate of Analysis	Mar 13, 2023	A413515
D2318063	Certificate of Analysis	Mar 13, 2023	A413515
D2318049	Certificate of Analysis	Mar 13, 2023	A413515
D2318061	Certificate of Analysis	Mar 13, 2023	A413515
D2318041	Certificate of Analysis	Mar 13, 2023	A413515
D2318058	Certificate of Analysis	Mar 13, 2023	A413515
D2318048	Certificate of Analysis	Mar 13, 2023	A413515
D2318052	Certificate of Analysis	Mar 13, 2023	A413515

Show more⌵

Chemical and Physical Properties

DMSO(mg / mL) Max Solubility	55
DMSO(mM) Max Solubility	200.466540311999
Water(mg / mL) Max Solubility	55
Water(mM) Max Solubility	200.466540311999
Molecular Weight	274.360 g/mol
XLogP3	-0.300
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	12
Exact Mass	274.189 Da
Monoisotopic Mass	274.189 Da
Topological Polar Surface Area	98.700 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	223.000
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	1

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.