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SDZ 205-557 hydrochloride - >99%, high purity , CAS No.137196-67-9, Antagonist of 5-HT 4 receptor

  • Moligand™
  • ≥99%
Item Number
S335718
Grouped product items
SKUSizeAvailabilityPrice Qty
S335718-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$113.90
S335718-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$484.90

a SR-3 and SR-4 antagonist

View related series
5-HT4 receptor Antagonist

Basic Description

Synonyms137196-67-9|2-(Diethylamino)ethyl 4-amino-5-chloro-2-methoxybenzoate|SDZ 205557|SDZ-205557|SDZ 205-557|SDZ-205-557|2-Methoxy-4-amino-5-chlorobenzoic acid 2-(diethylamino)ethyl ester|CHEMBL287045|Benzoic acid, 4-amino-5-chloro-2-methoxy-, 2-(diethylamino)e
Specifications & PurityMoligand™, ≥99%
Storage TempRoom temperature,Desiccated
Shipped InNormal
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of 5-HT 4 receptor
Product Description

SDZ 205-557 hydrochloride acts as a SR-3 and SR-4 antagonist.

Associated Targets

CYP1A2 Tchem Cytochrome P450 1A2 0 Activities

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

CYP2D6 Tclin Cytochrome P450 2D6 0 Activities

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

CYP2C19 Tchem Cytochrome P450 2C19 0 Activities

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

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

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

CYP2C9 Tchem Cytochrome P450 2C9 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)

SMN1 Tchem Survival motor neuron protein 0 Activities

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

TSHR Tclin Thyrotropin receptor 0 Activities

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

HTR4 Tclin 5-hydroxytryptamine receptor 4 2 Activities

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

CHRM1 Tclin Muscarinic acetylcholine receptor M1 0 Activities

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

HTR3A Tclin 5-hydroxytryptamine receptor 3A 1 Activities

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

ARSA Tbio Arylsulfatase A 0 Activities

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

Names and Identifiers

IUPAC Name 2-(diethylamino)ethyl 4-amino-5-chloro-2-methoxybenzoate
INCHI InChI=1S/C14H21ClN2O3/c1-4-17(5-2)6-7-20-14(18)10-8-11(15)12(16)9-13(10)19-3/h8-9H,4-7,16H2,1-3H3
InChi Key FFNWMBDISAYHDC-UHFFFAOYSA-N
Canonical SMILES CCN(CC)CCOC(=O)C1=CC(=C(C=C1OC)N)Cl
Isomeric SMILES CCN(CC)CCOC(=O)C1=CC(=C(C=C1OC)N)Cl
WGK Germany 3
PubChem CID 5191
Molecular Weight 300.78

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySoluble in DMSO (100 mg/mL), and water (65 mg/mL). Insoluble in ethanol.
Refractive Indexn20D1.55 (Predicted)

Safety and Hazards(GHS)

WGK Germany 3
RIDADR NONHforallmodesoftransport

Related Documents

Solution Calculators