Amodiaquin dihydrochloride dihydrate - 97%, high purity , Ferriprotoporphyrin IX inhibitor, CAS No.6398-98-7, Ferriprotoporphyrin IX inhibitor

  • ≥97%
Item Number
A135245
Grouped product items
SKUSizeAvailabilityPrice Qty
A135245-5g
5g
In stock
$24.90
A135245-25g
25g
In stock
$80.90
A135245-100g
100g
In stock
$290.90
View related series
Pharmaceutical ingredients

Basic Description

SynonymsAMODIAQUINI HYDROCHLORIDUM [WHO-IP LATIN] | HY-B1322 | NCGC00017063-01 | NSC 755863 | SN 10751 | Tox21_110765 | NSC-755863 | 6398-98-7 (HCl hydrate) | AMODIAQUINE HYDROCHLORIDE [ORANGE BOOK] | Amodiaquini hydrochloridum | Amodiaquin HCl hydrate | Amodiaqu
Specifications & Purity≥97%
Shipped InNormal
Action TypeINHIBITOR
Mechanism of actionFerriprotoporphyrin IX inhibitor

Associated Targets(Human)

CYP2D6 Tclin Cytochrome P450 2D6 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GMNN Tbio Geminin (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
HIF1A Tchem Hypoxia-inducible factor 1-alpha (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PMP22 Tbio Peripheral myelin protein 22 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALOX15B Tchem Arachidonate 15-lipoxygenase B (0 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)
ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HIF1A Tchem Hypoxia-inducible factor 1 alpha (6027 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PMP22 Tbio Peripheral myelin protein 22 (699 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

Pubchem Sid488183633
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183633
IUPAC Name 4-[(7-chloroquinolin-4-yl)amino]-2-(diethylaminomethyl)phenol;dihydrate;dihydrochloride
INCHI InChI=1S/C20H22ClN3O.2ClH.2H2O/c1-3-24(4-2)13-14-11-16(6-8-20(14)25)23-18-9-10-22-19-12-15(21)5-7-17(18)19;;;;/h5-12,25H,3-4,13H2,1-2H3,(H,22,23);2*1H;2*1H2
InChi Key YVNAYSHNIILOJS-UHFFFAOYSA-N
Canonical SMILES CCN(CC)CC1=C(C=CC(=C1)NC2=C3C=CC(=CC3=NC=C2)Cl)O.O.O.Cl.Cl
Isomeric SMILES CCN(CC)CC1=C(C=CC(=C1)NC2=C3C=CC(=CC3=NC=C2)Cl)O.O.O.Cl.Cl
PubChem CID 64646
Molecular Weight 464.81

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDateItem
B2317339Certificate of AnalysisDec 06, 2024 A135245
B2317318Certificate of AnalysisDec 06, 2024 A135245
B2317184Certificate of AnalysisDec 06, 2024 A135245
B2317252Certificate of AnalysisDec 21, 2022 A135245
B2317271Certificate of AnalysisDec 21, 2022 A135245
B2317277Certificate of AnalysisDec 21, 2022 A135245
D1524048Certificate of AnalysisNov 15, 2022 A135245

Chemical and Physical Properties

SolubilitySoluble in water; Soluble in Methanol; Very slightly soluble in Chloroform,Benzene,Ether; Insoluble in Alcohol

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H302:Harmful if swallowed

Precautionary Statements

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P330:Rinse mouth.

P301+P317:IF SWALLOWED: Get medical help.

Merck Index 572

Related Documents

Citations of This Product

1. Ying Pan, Qiongjie Ding, Baohong Li, Xiaoxiong Wang, Yiwei Liu, Junhao Chen, Fei Ke, Jianqiang Liu.  (2021)  Self-adjusted bimetallic zeolitic-imidazolate framework-derived hierarchical magnetic carbon composites as efficient adsorbent for optimizing drug contaminant removal.  CHEMOSPHERE,  263  (128101).  [PMID:33297097] [10.1016/j.chemosphere.2020.128101]

References

1. Ying Pan, Qiongjie Ding, Baohong Li, Xiaoxiong Wang, Yiwei Liu, Junhao Chen, Fei Ke, Jianqiang Liu.  (2021)  Self-adjusted bimetallic zeolitic-imidazolate framework-derived hierarchical magnetic carbon composites as efficient adsorbent for optimizing drug contaminant removal.  CHEMOSPHERE,  263  (128101).  [PMID:33297097] [10.1016/j.chemosphere.2020.128101]

Solution Calculators