CAS 2016-88-8|Amiloride hydrochloride

Introduction:Basic information about CAS 2016-88-8|Amiloride hydrochloride, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameAmiloride hydrochloride
CAS Number2016-88-8Molecular Weight266.088
Density2.11 g/cm3Boiling Point628.1ºC at 760 mmHg
Molecular FormulaC6H9Cl2N7OMelting Point293-294°C
MSDS/Flash Point333.7ºC

Names

Nameamiloride hydrochloride
SynonymMore Synonyms

Amiloride hydrochloride BiologicalActivity

DescriptionAmiloride (hydrochloride) is an epithelial sodium channel (ENaC) inhibitor and a competitive inhibitor of Urokinase-type plasminogen activator (uPA).
Related CatalogSignaling Pathways >>Membrane Transporter/Ion Channel >>Sodium ChannelResearch Areas >>Metabolic Disease
Target

ENaC, uPA[1]

In VitroAmiloride blocks δβγ channels with an IC50 of 2.6 μM. The Ki of amiloride for δβγ ENaC is 26-fold that of αβγ channels (0.1 μM for αβγ ENaC). Amiloride blockade of δβγ ENaC is much more voltage dependent compared with the αβγ channel. The Ki of amiloride for δαβγ channels is 920 and 13.7 μM at −120 and +80 mV, respectively, which significantly differs from that of both αβγ and δβγ channels[1]. Amiloride is a relatively selective inhibitor of the epithelial sodium channel (ENaC) with an IC50 (the concentration required to reach 50% inhibition of an ion channel) in the concentration range of 0.1 to 0.5 μM. Amiloride is a relatively poor inhibitor of the the Na+/H+ exchanger (NHE) with an IC50 as low as 3 μM in the presence of a low external [Na+] but as high as 1 mM in the presence of a high [Na+]. Amiloride is an even weaker inhibitor of the Na+/Ca2+ exchanger (NCX), with an IC50 of 1 mM. Amiloride (1 μM) and submicromolar doses of Benzamil (30 nM), doses known to inhibit the ENaC, inhibit the myogenic vasoconstriction response to increasing perfusion pressure by blocking the activity of ENaC proteins. Amiloride completely inhibits Na+ influx in doses known to be relatively specific for ENaC (1.5 μM) in vascular smooth muscle cells (VSMC)[2].
In VivoAmiloride (1 mg/kg/day) subcutaneously is found to reverse the initial increases in collagen deposition and prevent any further increases in the DOCA-salt hypertensive rat. Amiloride delays the onset of proteinuria and improved brain and kidney histologic scores in the saline-drinking, stroke-prone spontaneously hypertensive rats (SHRSP) compared with controls. Amiloride antagonizes or prevents actions of aldosterone in these cells and in cardiovascular and renal tissues in animals with salt-dependent forms of hypertension[2].
References

[1]. Ji, H.L., et al. delta ENaC: a novel divergent amiloride-inhibitable sodium channel. Am J Physiol Lung Cell Mol Physiol, 2012. 303(12): p. L1013-26.

[2]. Teiwes J, et al. Epithelial sodium channel inhibition in cardiovascular disease. A potential role for amiloride. Am J Hypertens. 2007 Jan;20(1):109-17.

Chemical & Physical Properties

Density2.11 g/cm3
Boiling Point628.1ºC at 760 mmHg
Melting Point293-294°C
Molecular FormulaC6H9Cl2N7O
Molecular Weight266.088
Flash Point333.7ºC
Exact Mass265.024567
PSA156.79000
LogP2.07300
Vapour Pressure1.08E-15mmHg at 25°C
InChIKeyACHKKGDWZVCSNH-UHFFFAOYSA-N
SMILESCl.NC(N)=NC(=O)c1nc(Cl)c(N)nc1N
Storage conditionStore at RT
Water SolubilityH2O: 50 mg/mL, clear, yellow-green | <0.1 g/100 mL at 19.5 ºC

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
UQ2275500
CHEMICAL NAME :
Pyrazinecarboxamide, N-amidino-3,5-diamino-6-chloro-, monohydrochloride
CAS REGISTRY NUMBER :
2016-88-8
LAST UPDATED :
199504
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C6-H8-Cl-N7-O.Cl-H
MOLECULAR WEIGHT :
266.12

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Mutation in microorganisms
TEST SYSTEM :
Bacteria - Salmonella typhimurium
DOSE/DURATION :
1 mg/plate
REFERENCE :
EMMUEG Environmental and Molecular Mutagenesis. (Alan R. Liss, Inc., 41 E. 11th St., New York, NY 10003) V.10- 1987- Volume(issue)/page/year: 19(Suppl 21),2,1992 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X3814 No. of Facilities: 32 (estimated) No. of Industries: 2 No. of Occupations: 9 No. of Employees: 4480 (estimated) No. of Female Employees: 1822 (estimated)

Safety Information

Hazard CodesT:Toxic
Risk PhrasesR25
Safety PhrasesS36-S45
RIDADRUN 2811 6.1/PG 3
WGK Germany3
RTECSUQ2275500
Packaging GroupII
Hazard Class6.1(a)
HS Code29339980

Customs

HS Code2934999090
Summary2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Synonyms

GUANAMPRAZINE
amiprazidine
2-Pyrazinecarboxamide, 3,5-diamino-N-(aminoiminomethyl)-6-chloro-, hydrochloride (1:1)
3,5-diamino-N-carbamimidoyl-6-chloropyrazine-2-carboxamide hydrochloride
N-Amidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride hydrate
3,5-Diamino-N-carbamimidoyl-6-chloropyrazine-2-carboxamide Hydrochloride Hydrate
Amiloridhydrochlorid
N-amidino-3,5-diamino-6-chloro-pyrazinecarboxamide hydrochloride
AMIPRAMIDIN
Amiloride HCl
3,5-Diamino-N-carbamimidoyl-6-chloro-2-pyrazinecarboxamide hydrochloride (1:1)
3,5-diamino-N-carbamimidoyl-6-chloropyrazine-2-carboxamide chlorhydrate
N-amidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride
3,5-diamino-N-[amino(imino)methyl]-6-chloropyrazine-2-carboxamide hydrochloride
Arumil
AMipraMidine
HCL AMILORIDE HCL
UNII-7M458Q65S3
Midamor
Pyrazinecarboxamide, 3,5-diamino-N-(aminoiminomethyl)-6-chloro-, monohydrochloride
3,5-Diamino-N-carbamimidoyl-6-chloropyrazine-2-carboxamide hydrochloride (1:1)
AMIPRAMIZIDE
amiloride monohydrochloride
amiloridechloride
Amiloride (hydrochloride)
Guanamprazine hydrochloride
AMipraMizi
EINECS 217-958-2
MFCD03703482
2-pyrazinecarboxamide, 3,5-diamino-N-(aminoiminomethyl)-6-chloro-, monohydrochloride
Amiloride hydrochloride
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