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Furosemide - ≥98%, high purity , Sodium-(potassium)-chloride cotransporter 2 inhibitor, CAS No.54-31-9, Sodium-(potassium)-chloride cotransporter 2 inhibitor

Specifications & Purity: ≥98%

CAS#: 54-31-9
Formula: C₁₂H₁₁ClN₂O₅S
Molecular Weight: 330.74
EC Number: 200-203-6
MDL number: MFCD00010549
PubChem CID: 3440

Item Number

F129560

Grouped product items
SKU	Size	Availability	Price
F129560-1g	1g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$64.90
F129560-5g	5g	In stock	$195.90
F129560-25g	25g	In stock	$882.90
F129560-100g	100g	In stock	$3,175.90

Inhibitor of the Na + /2Cl - /K + cotransporter. Also GABA A antagonist.

View related series

Basolateral Na-K-Cl symporter Inhibitor GABAA receptor α6 subunit Allosteric modulator GPR35 Agonist Kidney-specific Na-K-Cl symporter Inhibitor

Basic Description

Synonyms	furosemide\|54-31-9\|Frusemide\|Lasix\|Furanthril\|Furosemid\|Errolon\|Fusid\|Aisemide\|Beronald\|Desdemin\|Frusemin\|Fuluvamide\|Furanthryl\|Furantril\|Fursemide\|Lowpstron\|Macasirool\|Prefemin\|Rosemide\|Trofurit\|Fulsix\|Furesis\|Katlex\|Lasilix\|Radonna\|Seguril\|Transit\|Lasex
Specifications & Purity	≥98%
Storage Temp	Store at -20°C
Shipped In	Dry ice
Action Type	AGONIST, ALLOSTERIC MODULATOR, INHIBITOR
Mechanism of action	Sodium-(potassium)-chloride cotransporter 2 inhibitor

Associated Targets

GPR35 Tchem G-protein coupled receptor 35 0 Activities

Discover Target: GPR35

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA5A Tclin Carbonic anhydrase 5A, mitochondrial 1 Activities

Discover Target: CA5A

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

GABRA6 Tclin Gamma-aminobutyric acid receptor subunit alpha-6 0 Activities

Discover Target: GABRA6

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC12A1 Tclin Solute carrier family 12 member 1 1 Activities

Discover Target: SLC12A1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC12A2 Tclin Solute carrier family 12 member 2 1 Activities

Discover Target: SLC12A2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA5B Tclin Carbonic anhydrase 5B, mitochondrial 1 Activities

Discover Target: CA5B

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA6 Tclin Carbonic anhydrase 6 1 Activities

Discover Target: CA6

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA1 Tclin Carbonic anhydrase 1 1 Activities

Discover Target: CA1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 1 Activities

Discover Target: CA2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA4 Tclin Carbonic anhydrase 4 1 Activities

Discover Target: CA4

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA12 Tclin Carbonic anhydrase 12 1 Activities

Discover Target: CA12

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA14 Tclin Carbonic anhydrase 14 1 Activities

Discover Target: CA14

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA9 Tclin Carbonic anhydrase 9 1 Activities

Discover Target: CA9

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA7 Tclin Carbonic anhydrase 7 1 Activities

Discover Target: CA7

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	4-chloro-2-(furan-2-ylmethylamino)-5-sulfamoylbenzoic acid
INCHI	InChI=1S/C12H11ClN2O5S/c13-9-5-10(15-6-7-2-1-3-20-7)8(12(16)17)4-11(9)21(14,18)19/h1-5,15H,6H2,(H,16,17)(H2,14,18,19)
InChi Key	ZZUFCTLCJUWOSV-UHFFFAOYSA-N
Canonical SMILES	C1=COC(=C1)CNC2=CC(=C(C=C2C(=O)O)S(=O)(=O)N)Cl
Isomeric SMILES	C1=COC(=C1)CNC2=CC(=C(C=C2C(=O)O)S(=O)(=O)N)Cl
WGK Germany	3
RTECS	CB2625000
PubChem CID	3440
Molecular Weight	330.74

DrugBank Ligand

Wikipedia

ChEBI

CAS Registry No.

PubChem CID

ChEMBL Ligand

RCSB PDB Ligand

PEP

DrugCentral Ligand

GPCRdb Ligand

Certificates

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14 results found

Lot Number	Certificate Type	Date	Item
H2205062	Certificate of Analysis	May 13, 2024	F129560
H2205063	Certificate of Analysis	May 13, 2024	F129560
H2205064	Certificate of Analysis	May 13, 2024	F129560
D2422230	Certificate of Analysis	Mar 25, 2024	F129560
D2422231	Certificate of Analysis	Mar 25, 2024	F129560
D2422232	Certificate of Analysis	Mar 25, 2024	F129560
D2422233	Certificate of Analysis	Mar 25, 2024	F129560
E2129157	Certificate of Analysis	Mar 13, 2023	F129560
E2129159	Certificate of Analysis	Mar 13, 2023	F129560
B1525035	Certificate of Analysis	Aug 12, 2022	F129560
A2418068	Certificate of Analysis	Jul 21, 2022	F129560
H2205065	Certificate of Analysis	Jul 21, 2022	F129560
J2307036	Certificate of Analysis	Jul 21, 2022	F129560
E2129158	Certificate of Analysis	Jun 03, 2021	F129560

Pictogram(s)

GHS08

Signal

Danger

Hazard Statements

H360

Precautionary Statements

P280,P405,P501,P203,P318

WGK Germany

RTECS

CB2625000

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