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Small Molecules & Compound Libraries
BC-1215 - 98%, high purity , CAS No.1507370-20-8

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BC-1215 - 98%, high purity , CAS No.1507370-20-8

COA

Grade & Purity:

≥98%

Cas Number: 1507370-20-8
Molecular Weight: 394.51
PubChem CID: 72201045
PubChem SID: 504772254

In stock

Item Number

B412321

Grouped product items
SKU	Size	Availability	Price
B412321-5mg	5mg	3	$75.90
B412321-10mg	10mg	3	$129.90
B412321-25mg	25mg	1	$271.90
B412321-50mg	50mg	1	$478.90
B412321-100mg	100mg	1	$826.90

E3 ligase Ligand

View related series

Ligands for E3 Ligase (39) PROTAC (2077)

Basic Description

Synonyms	BC-1215 \| 1507370-20-8 \| N1,N2-Bis(4-(pyridin-2-yl)benzyl)ethane-1,2-diamine \| N,N'-Bis[(4-pyridin-2-ylphenyl)methyl]ethane-1,2-diamine \| N1,N2-Bis[[4-(2-pyridinyl)phenyl]methyl]- 1,2-ethanediamine \| {[4-(PYRIDIN-2-YL)PHENYL]METHYL}[2-({[4-(PYRIDIN-2-YL)PHENYL]METH
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	BC-1215 is an inhibitor of F-box protein 3 (Fbxo3, a ubiquitin E3 ligase component) with IC50 of 0.9 μg/mL and LC50 of 87 μg/ml for IL-1β release. BC-1215 inhibits the Fbxo3-TRAF activation pathway by destabilizing TRAF1-6.
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	Information BC-1215 is an inhibitor of F-box protein 3 (Fbxo3, a ubiquitin E3 ligase component) with IC50 of 0.9 μg/mL and LC50 of 87 μg/ml for IL-1β release. BC-1215 inhibits the Fbxo3-TRAF activation pathway by destabilizing TRAF1-6. Targets IL-1β release (Cell-free assay); IL-1β release (Cell-free assay) 0.9 μg/mL; 87 μg/mL(LC50)

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Pyridines and derivatives
    - Subclass Phenylpyridines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Pyridines and derivatives
Subclass	Phenylpyridines
Intermediate Tree Nodes	Not available
Direct Parent	Phenylpyridines
Alternative Parents	Phenylmethylamines Benzylamines Aralkylamines Heteroaromatic compounds Dialkylamines Azacyclic compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	2-phenylpyridine - Phenylmethylamine - Benzylamine - Aralkylamine - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Azacycle - Secondary amine - Secondary aliphatic amine - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as phenylpyridines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyridine ring through a CC or CN bond.
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

Associated Targets(Human)

U-937 (7138 Activities)

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

Associated Targets(non-human)

Mus musculus (284745 Activities)

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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	504772254
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504772254
IUPAC Name	N,N'-bis[(4-pyridin-2-ylphenyl)methyl]ethane-1,2-diamine
INCHI	InChI=1S/C26H26N4/c1-3-15-29-25(5-1)23-11-7-21(8-12-23)19-27-17-18-28-20-22-9-13-24(14-10-22)26-6-2-4-16-30-26/h1-16,27-28H,17-20H2
InChIKey	IXEPQJQQSLMESJ-UHFFFAOYSA-N
Smiles	C1=CC=NC(=C1)C2=CC=C(C=C2)CNCCNCC3=CC=C(C=C3)C4=CC=CC=N4
Isomeric SMILES	C1=CC=NC(=C1)C2=CC=C(C=C2)CNCCNCC3=CC=C(C=C3)C4=CC=CC=N4
WGK Germany	3
Molecular Weight	394.51
Reaxy-Rn	24671086
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24671086&ln=

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

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

Analytical Chart:

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5 results found

Lot Number	Certificate Type	Date	Item
G2213501	Certificate of Analysis	Apr 07, 2025	B412321
G2213502	Certificate of Analysis	Apr 07, 2025	B412321
G2213504	Certificate of Analysis	Apr 07, 2025	B412321
G2213503	Certificate of Analysis	Apr 07, 2025	B412321
G2213505	Certificate of Analysis	Apr 07, 2025	B412321

Chemical and Physical Properties

Solubility	Solubility (25°C) In vitro DMSO: 79 mg/mL (200.24 mM); Ethanol: 79 mg/mL (200.24 mM); Water: Insoluble;
Molecular Weight	394.500 g/mol
XLogP3	3.500
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	9
Exact Mass	394.216 Da
Monoisotopic Mass	394.216 Da
Topological Polar Surface Area	49.800 Å²
Heavy Atom Count	30
Formal Charge	0
Complexity	412.000
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

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