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SKF-83566 , CAS No.S613610, Inhibitor of adenylyl cyclase 2;Antagonist of D 1 receptor;Antagonist of D 5 receptor

  • Moligand™
  • PubChem CID:   1243
Item Number
S613610
Grouped product items
SKUSizeAvailabilityPrice Qty
S613610-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,334.90
S613610-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$2,001.90

Basic Description

Synonyms99295-33-7|SKF-83566|SK&F-83566|Skf 83566|8-Bromo-3-methyl-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol|SK&F 83566|1H-3-Benzazepin-7-ol, 8-bromo-2,3,4,5-tetrahydro-3-methyl-5-phenyl-|D203LR7XUS|SK-83566|CHEMBL324017|8-bromo-3-methyl-5-phenyl-1,2,4,5
Specifications & PurityMoligand™
GradeMoligand™
Action TypeANTAGONIST, INHIBITOR
Mechanism of actionInhibitor of adenylyl cyclase 2;Antagonist of D 1 receptor;Antagonist of D 5 receptor

Associated Targets

DRD1 Tclin D(1A) dopamine receptor 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD2 Tclin D(2) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD5 Tchem D(1B) dopamine receptor 4 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADCY3 Tbio Adenylate cyclase type 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADCY1 Tchem Adenylate cyclase type 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADCY2 Tchem Adenylate cyclase type 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 7-bromo-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol
INCHI InChI=1S/C17H18BrNO/c1-19-8-7-13-9-16(18)17(20)10-14(13)15(11-19)12-5-3-2-4-6-12/h2-6,9-10,15,20H,7-8,11H2,1H3
InChi Key XFTVOHWWEQGXLS-UHFFFAOYSA-N
Canonical SMILES CN1CCc2c(C(C1)c1ccccc1)cc(c(c2)Br)O
Isomeric SMILES CN1CCC2=CC(=C(C=C2C(C1)C3=CC=CC=C3)O)Br
PubChem CID 1243

Certificates

Certificate of Analysis(COA)

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Related Documents

References

1. Sunahara RK, Guan HC, O'Dowd BF, Seeman P, Laurier LG, Ng G, George SR, Torchia J, Van Tol HH, Niznik HB.  (1991)  Cloning of the gene for a human dopamine D5 receptor with higher affinity for dopamine than D1..  Nature,  350  (6319): (614-9).  [PMID:1826762]
2. Bakthavachalam V, Baindur N, Madras BK, Neumeyer JL.  (1991)  Fluorescent probes for dopamine receptors: synthesis and characterization of fluorescein and 7-nitrobenz-2-oxa-1,3-diazol-4-yl conjugates of D-1 and D-2 receptor ligands..  J Med Chem,  34  (11): (3235-41).  [PMID:1956042]
3. Conley JM, Brand CS, Bogard AS, Pratt EP, Xu R, Hockerman GH, Ostrom RS, Dessauer CW, Watts VJ.  (2013)  Development of a high-throughput screening paradigm for the discovery of small-molecule modulators of adenylyl cyclase: identification of an adenylyl cyclase 2 inhibitor..  J Pharmacol Exp Ther,  347  (2): (276-87).  [PMID:24008337]

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