AC 265347 - Moligand™, ≥97% , Allosteric modulator of CaS receptor, CAS No.1253901-26-6, Allosteric modulator of CaS receptor

CAS: 1253901-26-6 Cat. No.: A288466 Formula: C₁₇H₁₇NOS Peso molecolare: 283.39 Numero EC: 694-385-8

GRADE & PURITY Moligand™, ≥97%

Synonyms

AC265347 | AC-265347 | SCHEMBL19462840 | AC-265347, >=98% (HPLC) | Q27074133 | 1-(Benzo[d]thiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol | 1253901-26-6 | AKOS027324495 | J-005222 | HY-117851 | ?-(2,4-Dimethylphenyl)-?-methyl-2-benzothiazolemethanol | MLS0060

Storage

Conservare a 2-8°C, al riparo dalla luce

Shipped In

Ghiaccio umido

Panoramica

Modulatore allosterico sbilanciato del recettore sensibile al calcio (CaSR)

Applicazione: AC 265347 è un modulatore allosterico

AC 265347 è un modulatore allosterico polarizzato del CaSR (pEC50 = 7,8-8,1). Calcimetico. Mostra la capacità di orientare la segnalazione verso l'accumulo di pERK1/2 e IP1. Riduce i livelli di ormone paratiroideo (PTH) nel siero di ratto senza indurre il rilascio di calcitonina. Non mostra un'attivazione significativa dei recettori GABAB umani o del PTH di tipo I. Attivo per via orale.

Specifications

Sinonimi

AC265347 | AC-265347 | SCHEMBL19462840 | AC-265347, >=98% (HPLC) | Q27074133 | 1-(Benzo[d]thiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol | 1253901-26-6 | AKOS027324495 | J-005222 | HY-117851 | ?-(2,4-Dimethylphenyl)-?-methyl-2-benzothiazolemethanol | MLS0060

Specifiche e purezza

Moligand™, ≥97%

Meccanismi biochimici e fisiologici

Modulatore allosterico CaSR biased (pEC50= 7,8-8,1). Calcimetico. Dimostra la capacità di orientare la segnalazione verso l'accumulo di pERK1/2 e IP1. Riduce i livelli di ormone paratiroideo (PTH) nel siero di ratto senza indurre il rilascio di calcitonin

Condizioni di conservazione di stoccaggio

Conservare a 2-8°C, al riparo dalla luce

Spedito in

Ghiaccio umido

Grado

Moligand™

Tipo di azione

ALLOSTERIC MODULATOR

Meccanismo d'azione

Allosteric modulator of CaS receptor

Purezza

≥97%

Nomi e identificatori

• Pubchem Sid: 528763014
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/528763014
• Sorrisi canonici: CC1=CC(=C(C=C1)C(C)(C2=NC3=CC=CC=C3S2)O)C
• IUPAC Name: 1-(1,3-benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol
• InChIKey: IGSZVEPQZANNAB-UHFFFAOYSA-N
• INCHI: 1S/C17H17NOS/c1-11-8-9-13(12(2)10-11)17(3,19)16-18-14-6-4-5-7-15(14)20-16/h4-10,19H,1-3H3
• Isomeri SMILES: CC1=CC(=C(C=C1)C(C)(C2=NC3=CC=CC=C3S2)O)C
• CAS alternativo: 1253901-26-6
• Termini MeSH: 1-(1,3-benzothiazol-2-yl)-1-(2,4-dimethylphenyl)ethanol;AC265347
• Peso molecolare: 283.39
• Reaxy-Rn: 20798213
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=20798213&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Benzothiazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Benzothiazoles
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzothiazoles
• Alternative Parents: m-Xylenes Thiazoles Tertiary alcohols Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: 1,3-benzothiazole - M-xylene - Xylene - Monocyclic benzene moiety - Benzenoid - Azole - Heteroaromatic compound - Tertiary alcohol - Thiazole - Azacycle - Alcohol - Aromatic alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as benzothiazoles. These are organic compounds containing a benzene fused to a thiazole ring (a five-membered ring with four carbon atoms, one nitrogen atom and one sulfur atom).
• 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.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

CASR Tclin Extracellular calcium-sensing receptor (1 Activities)

Discover Target: CASR

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)

Discover Target: ABL1

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

ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

Discover Target: ADRB2

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

ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

Discover Target: ADRA2A

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

AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)

Discover Target: AGTR1

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

PTH1R Tclin Parathyroid hormone receptor (47172 Activities)

Discover Target: PTH1R

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

CASR Tclin Calcium sensing receptor (766 Activities)

Discover Target: CASR

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

GSK3B Tclin Glycogen synthase kinase-3 beta (11785 Activities)

Discover Target: GSK3B

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

CSNK1D Tchem Casein kinase I delta (4546 Activities)

Discover Target: CSNK1D

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

S1PR1 Tclin Sphingosine 1-phosphate receptor Edg-1 (5806 Activities)

Discover Target: S1PR1

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

CDK2 Tchem Cyclin-dependent kinase 2 (9050 Activities)

Discover Target: CDK2

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

GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)

Discover Target: GLP1R

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

C5AR1 Tclin C5a anaphylatoxin chemotactic receptor (2677 Activities)

Discover Target: C5AR1

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

AURKA Tchem Serine/threonine-protein kinase Aurora-A (10240 Activities)

Discover Target: AURKA

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

U2OS (164939 Activities)

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

CX3CR1 Tchem C-X3-C chemokine receptor 1 (1686 Activities)

Discover Target: CX3CR1

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

FPR2 Tchem Lipoxin A4 receptor (3472 Activities)

Discover Target: FPR2

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

FFAR4 Tchem G-protein coupled receptor 120 (2999 Activities)

Discover Target: FFAR4

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

Liver microsomes (16955 Activities)

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

BRD4 Tchem Bromodomain-containing protein 4 (13122 Activities)

Discover Target: BRD4

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

GPR35 Tchem G-protein coupled receptor 35 (2643 Activities)

Discover Target: GPR35

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

TRIM24 Tchem Transcription intermediary factor 1-alpha (2087 Activities)

Discover Target: TRIM24

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

BRPF1 Tchem Peregrin (2217 Activities)

Discover Target: BRPF1

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

HEK-293T (167025 Activities)

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

Obiettivi associati (non umani)

Aplnr Apelin receptor (201 Activities)

Discover Target: Aplnr

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

Mapk1 MAP kinase ERK2 (650 Activities)

Discover Target: Mapk1

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

Fgfr3 Fibroblast growth factor receptor 3 (21 Activities)

Discover Target: Fgfr3

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

Rattus norvegicus (775804 Activities)

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

Gpr119 Glucose-dependent insulinotropic receptor (270 Activities)

Discover Target: Gpr119

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Solvent:DMSO, Max Conc. mg/mL: 28.34, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 28.34, Max Conc. mM: 100
• Sensibilità: Light sensitive
• Peso molecolare: 283.400 g/mol
• XLogP3: 4.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 283.103 Da
• Monoisotopic Mass: 283.103 Da
• Topological Polar Surface Area: 61.400 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 350.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1