2-[(1r,4r)-4-{4-[(2R)-4-[(2-ethylphenyl)carbamoyl]-2-methyl-3,4-dihydro-2H-1,4-benzoxazin-7-yl]phenyl}cyclohexyl]acetic acid , CAS No.R608967, Inhibitor of diacylglycerol O-acyltransferase 1

Item Number
R608967
Grouped product items
SKUSizeAvailabilityPrice Qty
R608967-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$570.90
R608967-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$2,000.90

Basic Description

Specifications & PurityMoligand™
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of diacylglycerol O-acyltransferase 1

Associated Targets(Human)

DGAT1 Tclin Diacylglycerol O-acyltransferase 1 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGIR Tclin Prostanoid IP receptor (1280 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CASP8 Tchem Caspase-8 (1006 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CASP9 Tchem Caspase-9 (154 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Caco-2 (12174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Canis familiaris (36305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rhesus monkey (3147 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences
Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

DailyMed: [1]


Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

DailyMed: [1]


Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

DailyMed: [1]


Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

DailyMed: [1]


Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

DailyMed: [1]


Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

DailyMed: [1]


Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

DailyMed: [1]


PubMed: [1] , [2]


Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

DailyMed: [1]


Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

PubMed: [1] , [2]


Epidermal growth factor receptor erbB1 inhibitorINHIBITORALA203Epidermal growth factor receptor erbB1SINGLE PROTEINHomo sapiens

PubMed: [1]


Names and Identifiers

IUPAC Name 2-[(1r,4r)-4-{4-[(2R)-4-[(2-ethylphenyl)carbamoyl]-2-methyl-3,4-dihydro-2H-1,4-benzoxazin-7-yl]phenyl}cyclohexyl]acetic acid
INCHI InChI=1S/C32H36N2O4/c1-3-23-6-4-5-7-28(23)33-32(37)34-20-21(2)38-30-19-27(16-17-29(30)34)26-14-12-25(13-15-26)24-10-8-22(9-11-24)18-31(35)36/h4-7,12-17,19,21-22,24H,3,8-11,18,20H2,1-2H3,(H,33,37)(H,35,36)/t21-,22-,24-/m1/s1
InChi Key PUQLADUSPHHAJY-CQOQZXRMSA-N
Canonical SMILES CCc1ccccc1NC(=O)N1C[C@@H](C)Oc2c1ccc(c2)c1ccc(cc1)[C@@H]1CC[C@H](CC1)CC(=O)O
Isomeric SMILES CCC1=CC=CC=C1NC(=O)N2C[C@H](OC3=C2C=CC(=C3)C4=CC=C(C=C4)C5CCC(CC5)CC(=O)O)C
PubChem CID 86277844

Certificates

C of A & Other Certificates

Related Documents

References

1. Zhou G, Zorn N, Ting P, Aslanian R, Lin M, Cook J, Lachowicz J, Lin A, Smith M, Hwa J et al..  (2014)  Development of novel benzomorpholine class of diacylglycerol acyltransferase I inhibitors..  ACS Med Chem Lett,  (5): (544-9).  [PMID:24900877] [10.1021/op500134e]

Solution Calculators