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GPCR/G Protein
5-HT Receptor
SDZ 205-557 hydrochloride - ≥99%(HPLC), high purity , CAS No.1197334-02-3

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SDZ 205-557 hydrochloride - ≥99%(HPLC), high purity , CAS No.1197334-02-3

COA

Grade & Purity:

≥99%(HPLC)

Cas Number: 1197334-02-3
Molecular Weight: 337.25
PubChem CID: 11957705
PubChem SID: 504766831

In stock

Item Number

S287656

Grouped product items
SKU	Size	Availability	Price
S287656-5mg	5mg	3	$87.90
S287656-10mg	10mg	2	$134.90
S287656-25mg	25mg	2	$303.90
S287656-50mg	50mg	1	$496.90
S287656-100mg	100mg	1	$894.90

5-HT3and 5-HT4antagonist

View related series

Class A GPCR (4138)

Basic Description

Synonyms	1197334-02-3 \| sdz 205-557 hcl \| LP01153 \| SR-01000075581-1 \| NCGC00015916-02 \| NCGC00092301-01 \| (2E)-3-{6-[(1E)-1-(4-methylphenyl)-3-(pyrrolidin-1-yl)prop-1-en-1-yl]pyridin-2-yl}acrylic acid \| Tox21_501153 \| 2-(DIETHYLAMINO)ETHYL 4-AMINO-5-CHLORO-2-METH
Specifications & Purity	≥99%(HPLC)
Biochemical and Physiological Mechanisms	5-HT3/5-HT4receptor antagonist.
Storage Temp	Store at -20°C,Desiccated
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Product Describtion: 5-HT3/5-HT4 receptor antagonist

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Benzoic acids and derivatives
      - Level5 Methoxybenzoic acids and derivatives
        Level6 O-methoxybenzoic acids and derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Benzoic acids and derivatives
Intermediate Tree Nodes	Methoxybenzoic acids and derivatives
Direct Parent	O-methoxybenzoic acids and derivatives
Alternative Parents	3-halobenzoic acids and derivatives Aminobenzoic acids and derivatives Benzoic acid esters Methoxyanilines Aminophenyl ethers Phenoxy compounds Methoxybenzenes Anisoles Benzoyl derivatives Alkyl aryl ethers Chlorobenzenes Aryl chlorides Trialkylamines Amino acids and derivatives Carboxylic acid esters Monocarboxylic acids and derivatives Hydrocarbon derivatives Hydrochlorides Organic oxides Organochlorides Organopnictogen compounds Primary amines
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	O-methoxybenzoic acid or derivatives - Aminobenzoic acid or derivatives - Benzoate ester - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Aminophenyl ether - Methoxyaniline - Anisole - Phenoxy compound - Benzoyl - Phenol ether - Aniline or substituted anilines - Methoxybenzene - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Tertiary amine - Carboxylic acid derivative - Ether - Monocarboxylic acid or derivatives - Organic oxygen compound - Organohalogen compound - Organic nitrogen compound - Organochloride - Amine - Hydrocarbon derivative - Organopnictogen compound - Organic oxide - Hydrochloride - Organooxygen compound - Primary amine - Organonitrogen compound - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as o-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 2 of the benzene ring is replaced by a methoxy group.
External Descriptors	Not available
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

Associated Targets(Human)

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

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

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)

Explore this target

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

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504766831
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504766831
IUPAC Name	2-(diethylamino)ethyl 4-amino-5-chloro-2-methoxybenzoate;hydrochloride
INCHI	InChI=1S/C14H21ClN2O3.ClH/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;1H
InChIKey	JOWUQCJWCRNVMQ-UHFFFAOYSA-N
Smiles	CCN(CC)CCOC(=O)C1=CC(=C(C=C1OC)N)Cl.Cl
Isomeric SMILES	CCN(CC)CCOC(=O)C1=CC(=C(C=C1OC)N)Cl.Cl
PubChem CID	11957705
Molecular Weight	337.25

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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.

5 results found

Lot Number	Certificate Type	Date	Item
G2209345	Certificate of Analysis	Apr 03, 2025	S287656
G2209349	Certificate of Analysis	Apr 03, 2025	S287656
G2209360	Certificate of Analysis	Apr 03, 2025	S287656
G2209351	Certificate of Analysis	Apr 03, 2025	S287656
G2209359	Certificate of Analysis	Apr 03, 2025	S287656

Chemical and Physical Properties

Solubility	Solvent:water, Max Conc. mg/mL: 33.73, Max Conc. mM: 100
Molecular Weight	337.200 g/mol
XLogP3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	8
Exact Mass	336.101 Da
Monoisotopic Mass	336.101 Da
Topological Polar Surface Area	64.800 Å²
Heavy Atom Count	21
Formal Charge	0
Complexity	300.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	2

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