BMS-8 - ≥98% , CAS No.1675201-90-7

CAS: 1675201-90-7 Cat. No.: B649237 Fórmula: C27H28BrNO3 Peso molecular: 494.42 PubChem CID: 117941742
Disponible para pedir
CALIDAD & PUREZA ≥98%
Synonyms
1-(3-Bromo-4-((2-methyl-[1,1'-biphenyl]-3-yl)methoxy)benzyl)piperidine-2-carboxylic acid|1-[3-Bromo-4-(2-methyl-biphenyl-3-ylmethoxy)-benzyl]-piperidine-2-carboxylic acid
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
★
Talla
USA
Alemania (EU)*
Precio
Cantidad
1mg
B649237-1mg
1 Disponible
—
60,90US$
5mg
B649237-5mg
1 Disponible
—
153,90US$
10mg
B649237-10mg
1 Disponible
—
246,90US$
25mg
B649237-25mg
1 Disponible
—
523,90US$
50mg
B649237-50mg
1 Disponible
—
777,90US$
100mg
B649237-100mg
1 Disponible
—
1.115,90US$
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Descripción general

BMS-8 inhibits the PD-1/PD-L1 interaction with IC 50 of 7.2 μM. BMS-8, binds directly to PD-L1 and induces formation of PD-L1 homodimers, which in turn prevents the interaction with PD-1.

In Vitro

BMS-8 tends to have a more stable binding mode with one PD-L1 monomer than the other and the small-molecule inducing PD-L1 dimerization was further stabilized by the non-polar interaction of Ile54, Tyr56, Met115, Ala121, and Tyr123 on both monomers and the water bridges involved in ALys124. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

Especificaciones

Sinónimos
1-(3-Bromo-4-((2-methyl-[1,1'-biphenyl]-3-yl)methoxy)benzyl)piperidine-2-carboxylic acid | 1-[3-Bromo-4-(2-methyl-biphenyl-3-ylmethoxy)-benzyl]-piperidine-2-carboxylic acid
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
BMS-8 inhibits the PD-1/PD-L1 interaction with IC 50 of 7.2 μM. BMS-8, binds directly to PD-L1 and induces formation of PD-L1 homodimers, which in turn prevents the interaction with PD-1.
Condiciones de almacenamiento de almacenamiento
Protected from light,Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Pureza
≥98%
Nombres e identificadores
Pubchem Sid
Sonrisas canónicas
CC1=C(C=CC=C1C2=CC=CC=C2)COC3=C(C=C(C=C3)CN4CCCCC4C(=O)O)Br
IUPAC Name
1-[[3-bromo-4-[(2-methyl-3-phenylphenyl)methoxy]phenyl]methyl]piperidine-2-carboxylic acid
InChIKey
QRXBPPWUGITQLE-UHFFFAOYSA-N
INCHI
1S/C27H28BrNO3/c1-19-22(10-7-11-23(19)21-8-3-2-4-9-21)18-32-26-14-13-20(16-24(26)28)17-29-15-6-5-12-25(29)27(30)31/h2-4,7-11,13-14,16,25H,5-6,12,15,17-18H2,1H3,(H,30,31)
Isómeros SMILES
CC1=C(C=CC=C1C2=CC=CC=C2)COC3=C(C=C(C=C3)CN4CCCCC4C(=O)O)Br
PubChem CID
117941742
Peso molecular
494.42

Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasePiperidines
SubclassBenzylpiperidines
Intermediate Tree Nodes Not available
Direct ParentN-benzylpiperidines
Alternative Parents Biphenyls and derivatives  Alpha amino acids  Piperidinecarboxylic acids  Phenylmethylamines  Phenoxy compounds  Phenol ethers  Benzylamines  Toluenes  Bromobenzenes  Aralkylamines  Alkyl aryl ethers  Aryl bromides  Trialkylamines  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organobromides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents N-benzylpiperidine - Biphenyl - Alpha-amino acid or derivatives - Alpha-amino acid - Piperidinecarboxylic acid - Phenoxy compound - Phenylmethylamine - Phenol ether - Benzylamine - Aralkylamine - Toluene - Halobenzene - Bromobenzene - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Aryl halide - Aryl bromide - Amino acid - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Azacycle - Monocarboxylic acid or derivatives - Ether - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Carbonyl group - Amine - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as n-benzylpiperidines. These are heterocyclic Compounds containing a piperidine ring conjugated to a benzyl group through one nitrogen ring atom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CD274 Tclin Programmed cell death 1 ligand 1 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CD274 Tclin Programmed cell death 1 ligand 1 (299 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
MC-38 (857 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

12 results found

Lot NumberCertificate TypeFechaArticulo
I2414437I2414437Certificate of AnalysisSep 09, 2024 B649237
I2414450I2414450Certificate of AnalysisSep 09, 2024 B649237
I2414451I2414451Certificate of AnalysisSep 09, 2024 B649237
I2414452I2414452Certificate of AnalysisSep 09, 2024 B649237
I2414453I2414453Certificate of AnalysisSep 09, 2024 B649237
I2414454I2414454Certificate of AnalysisSep 09, 2024 B649237
I2414455I2414455Certificate of AnalysisSep 09, 2024 B649237
I2414456I2414456Certificate of AnalysisSep 09, 2024 B649237
I2414457I2414457Certificate of AnalysisSep 09, 2024 B649237
I2414458I2414458Certificate of AnalysisSep 09, 2024 B649237
I2414459I2414459Certificate of AnalysisSep 09, 2024 B649237
I2414460I2414460Certificate of AnalysisSep 09, 2024 B649237
Propiedades químicas y físicas
SolubilidadDMSO : 83.33 mg/mL (168.54 mM; Need ultrasonic)
SensibilidadLight Sensitive
Peso molecular494.400 g/mol
XLogP34.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count7
Exact Mass493.125 Da
Monoisotopic Mass493.125 Da
Topological Polar Surface Area49.800 Ų
Heavy Atom Count32
Formal Charge0
Complexity595.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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