Diclofenamid

Dichlorphenamide

HCID 3038CAS 120-97-8

Grundinformationen

Standard-SMILES
NS(=O)(=O)c1cc(Cl)c(Cl)c(S(N)(=O)=O)c1
InChIKey
GJQPMPFPNINLKP-UHFFFAOYSA-N
Summenformel
C6H6Cl2N2O4S2
Durchschnittliche Molmasse
305,2 g/mol
Monoisotopische Masse
303,91460403

Überblick

Dichlorphenamide can cause developmental toxicity according to state or federal government labeling requirements.

Namen und Bezeichner

Bevorzugter Name
Dichlorphenamide
IUPAC
4,5-dichlorobenzene-1,3-disulfonamide
Lokaler Name
Diclofenamid
Englischer Name
Dichlorphenamide
Summenformel
C6H6Cl2N2O4S2
Molmasse
305.16

Namen und Synonyme

dichlorphenamideDiclofenamide120-97-84,5-dichlorobenzene-1,3-disulfonamideDichlorophenamideDichlofenamideDaranideAntidrasiGlaucolOratrol1,3-Benzenedisulfonamide, 4,5-dichloro-Dichlorphenamid
Weitere Namen anzeigen
cb8000CB 8000GlaucorOralconDalanidedaramide
DiclofenamidDiclofenamidaDiclofenamidum4,5-Dichloro-m-benzenedisulfonamide1,3-Disulfamyl-4,5-dichlorobenzene1,3-Disulfamoyl-4,5-dichlorobenzene4,5-Dichloro-1,3-disulfamoylbenzeneKeveyis

Datenbank-Bezeichner

CAS
120-97-8
PubChem CID
3038
DTXSID
DTXSID1022922
ChEMBL
CHEMBL17
ChEBI
CHEBI:101085
UNII
VVJ6673MHY
EC Number
204-440-6
Nikkaji
J8.589H

Eigenschaften

Berechnete Struktureigenschaften

XLogP
0,3
Polarare Oberfläche (TPSA)
137 Ų
H-Brücken-Donoren
2
H-Brücken-Akzeptoren
6
Frei drehbare Bindungen
2
Schwere Atome
16

Experimentelle und physikochemische Eigenschaften

DrugsPharmaceuticals -> Listed in ZINC15
LogP · 2 Einträge

0.2

0.92

OdorSLIGHT CHARACTERISTIC ODOR
Color/Form · 2 Einträge

NEEDLES FROM DIMETHYLSULFOXIDE + WATER

WHITE OR NEARLY WHITE, CRYSTALLINE POWDER

Solubility · 3 Einträge

PRACTICALLY INSOL IN WATER; SOL IN ALKALINE SOLN

FREELY SOL IN PYRIDINE & IN 1 N NAOH; SOL IN ALCOHOL; SOL IN 2 N SODIUM CARBONATE; SLIGHTLY SOL IN ETHER

3.98e-01 g/L

Human Drugs · 3 Einträge

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

Pharmaceuticals

Physikochemische Eigenschaften

Schmelzpunkt
239 · 239-241° (patent, mp 228.5-229°)
Siedepunkt
590.5 · 590.5±60.0 °C(Predicted)
Dichte
1.7263 · 1.7263 (rough estimate)
Brechungsindex
1.6 · 1.6000 (estimate)
storage temp.
Sealed in dry,Room Temperature
Löslichkeit
Acetonitrile (Slightly), Chloroform, DMSO (Slightly), Methanol

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 4 Einträge

Warning

H315 (50%): Causes skin irritation [Warning Skin corrosion/irritation]

P203, P264, P264+P265, P280, P302+P352, P305+P351+P338, P318, P321, P332+P317, P337+P317, P362+P364, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Regulatory Information · 2 Einträge

Hazard Traits - Developmental Toxicity

1,3-Benzenedisulfonamide, 4,5-dichloro-: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.

Other Safety InformationIMAP assessments - 1,3-Benzenedisulfonamide, 4,5-dichloro-: Environment tier I assessment
Hazard Classes and CategoriesSkin Irrit. 2 (50%)

Toxikologische Informationen

Human Toxicity Excerpts · 5 Einträge

CALCULUS FORMATION & URETERAL COLIC HAVE BEEN ATTRIBUTED TO MARKED REDN IN URINARY CITRATE...ASSOC WITH EITHER NO CHANGE OR EVEN RISE IN URINARY CALCIUM. ...DEPRESSES UPTAKE OF IODINE BY THYROID GLAND. /ACETAZOLAMIDE/

WITH LARGE DOSES, MANY PT EXHIBIT DROWSINESS & PARESTHESIAS. IN HEPATIC CIRRHOSIS, EPISODES OF DISORIENTATION MAY BE INDUCED. ... HYPERSENSITIVITY REACTIONS ARE RELATIVELY RARE. THEY CONSIST IN FEVER, SKIN REACTIONS, BONE-MARROW DEPRESSION, & SULFONAMIDE-LIKE RENAL LESIONS. /CARBONIC ANHYDRASE INHIBITORS/

LESS FREQUENT UNTOWARD REACTIONS INCL FATIGUE, EXCITEMENT, & GI REACTIONS. /CARBONIC ANHYDRASE INHIBITORS/

GI DISTURBANCES...ANOREXIA, NAUSEA, VOMITING, DIARRHEA, WT LOSS, ALTERED TASTE & SMELL, CONSTIPATION, DRYNESS OF MOUTH, EXCESSIVE THIRST...ABDOMINAL DISTENTION...PARESTHESIA...NUMBNESS & TINGLING SENSATION...IN EXTREMITIES, TONGUE, &/OR MUCOCUTANEOUS JUNCTIONS OF LIPS OR ANUS /ADVERSE EFFECT, ORAL/

For more Human Toxicity Excerpts (Complete) data for DICHLORPHENAMIDE (6 total), please visit the HSDB record page.

Drug Induced Liver Injury · 6 Einträge

Drug Induced Liver Injury Rank (DILIrank 2.0)

Dichlorphenamide

vNo-DILI-concern

0

No match

DOI:10.1016/j.drudis.2016.02.015

Non-Human Toxicity ExcerptsANIMAL STUDIES INDICATE SOME TERATOGENIC EFFECTS...

Sicherheitsdaten

wgk
WGK 3
hs_code
2935904000
RTECS-Nr.
CZ9200000
risk_code
63
hazard_code
Xn
safety_code
36

Chemie und Industrie

Pharmakologische Informationen

ATC Code · 2 Einträge

S - Sensory organs

QS - Sensory organs

Protein Binding55%
Pharmacodynamics · 1 Eintrag

Dichlorphenamide is an oral carbonic anhydrase inhibitor indicated for adjunctive treatment of: chronic simple (open-angle) glaucoma, secondary glaucoma, and preoperatively in acute angle-closure glaucoma where delay of surgery is desired in order to lower intraocular pressure. Carbonic anhydrase inhibitors reduce intraocular pressure by partially suppressing the secretion of aqueous humor (inflow).

Mechanism of Action · 6 Einträge

Carbonic anhydrase inhibitors reduce intraocular pressure by partially suppressing the secretion of aqueous humor (inflow), although the mechanism by which they do this is not fully understood. Evidence suggests that HCO<sup>3-</sup> ions are produced in the ciliary body by hydration of carbon dioxide under the influence of carbonic anhydrase and diffuse into the posterior chamber which contains more Na<sup>+</sup> and HCO<sup>3-</sup> ions than does plasma and consequently is hypertonic. Water is then attracted to the posterior chamber by osmosis, resulting in a drop in pressure.

PHOSPHATURIA MAY BE RELATED TO DIRECT STIMULATION...OF CYCLIC ADENOSINE 3',5'-MONOPHOSPHATE...PRODN BY KIDNEY. ...DRUG ACTS SIMILARLY TO PARATHYROID HORMONE IN ENHANCING URINARY EXCRETION OF PHOSPHATE & CYCLIC AMP, IN CONTRAST TO ITS ANTAGONISM OF ACTION OF HORMONE ON BONE. /ACETAZOLAMIDE/

...INHIBITION OF...CARBONIC ANHYDRASE. ...IS NONCOMPETITIVE. ...ENZYME IS NORMALLY PRESENT IN TISSUES IN HUGE EXCESS. MORE THAN 99% OF ENZYME ACTIVITY IN KIDNEY MUST BE INHIBITED BEFORE PHYSIOLOGICAL EFFECTS BECOME APPARENT. ENZYME...IS DOMINANT TISSUE COMPONENT TO WHICH INHIBITORS BECOME BOUND. /ACETAZOLAMIDE/

/CHANGES IN URINE/...MAY BE ATTRIBUTED TO INHIBITION OF (+)H SECRETION BY RENAL TUBULE. ... CURRENT EVIDENCE INDICATES GREATER EFFECT ON PROXIMAL THAN ON DISTAL TUBULE, WITH LITTLE OR NO EFFECT ON ASCENDING LIMB. ...PHOSPHATURIA...USED AS INDEX OF LOCALIZING DIURETIC ACTION... /ACETAZOLAMIDE/

...INCR URINARY EXCRETION OF BICARBONATE & FIXED CATION, MOSTLY SODIUM. AS RESULT, CONCN OF BICARBONATE IN EXTRACELLULAR FLUID DECR & METABOLIC ACIDOSIS RESULTS. ...RENAL RESPONSE TO ACETAZOLAMIDE IS GREATLY REDUCED.../BUT/ DIURETIC RESPONSE IS ENHANCED. /ACETAZOLAMIDE/

DRUG LOWERS INTRAOCULAR PRESSURE BY REDUCING RATE OF SECRETION OF AQ HUMOR.

FDA Pharmacological Classification · 6 Einträge

VVJ6673MHY

DICHLORPHENAMIDE

Established Pharmacologic Class [EPC] - Carbonic Anhydrase Inhibitor

Mechanisms of Action [MoA] - Carbonic Anhydrase Inhibitors

Chemical Structure [CS] - Sulfonamides

Dichlorphenamide is a Carbonic Anhydrase Inhibitor. The mechanism of action of dichlorphenamide is as a Carbonic Anhydrase Inhibitor.

MeSH Pharmacological ClassificationA class of compounds that reduces the secretion of H+ ions by the proximal kidney tubule through inhibition of CARBONIC ANHYDRASES.

Verwendung und Herstellung

UsesMEDICATION
Methods of ManufacturingSCHULTZ, US PATENT 2,835,702 (1958 TO MERCK & CO).
Formulations/PreparationsDICHLORPHENAMIDE, USP (DARANIDE), IS AVAIL AS OFFICIAL 50-MG TABLETS.
Use ClassificationPharmaceuticals
Anwendungen · 1 Eintrag

VerwendenLike the drugs described above, dichlorphenamide is used for secreting excess water in cases of elevated intraocular pressure, and it is used for treating wide-angle and secondary glaucoma as well as in cases where it is necessary to lower intraocular pressure before surgical intervention in severe wide-angle glaucoma.

Anbieter50 Anbieter

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
武汉英诺医药科技有限公司+86-027-59232304 15387063101 · [email protected]
艾吉析科技(上海)有限公司17717235263 · [email protected]
Ergänzende Hinweise · 1 Eintrag

DefinitionChEBI: A sulfonamide that is benzene-1,3-disulfonamide in which the hydrogens at positions 4 and 5 are substituted by chlorine. An oral carbonic anhydrase inhibitor, it partially suppresses the secretion (inflow) of aqueous humor in the eye and so reduces intraoc lar pressure. It is used for the treatment of glaucoma.

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