58-94-6NS(=O)(=O)c1cc2c(cc1Cl)NC=NS2(=O)=OJBMKAUGHUNFTOL-UHFFFAOYSA-NCrystals; white powder. (NTP, 1992)
58-94-6DTXSID0022800CHEMBL842CHEBI:3640Pharmaceuticals -> Listed in ZINC15
Pharmaceuticals -> Metabolite of Hydrochlorthiazide
log Kow = -0.24
-0.5
-0.1
Crystals
WHITE OR PRACTICALLY WHITE
less than 1 mg/mL at 67.1 °F (NTP, 1992)
SOL IN WATER: 0 G/L @ PH 4, 0.65 G/L @ PH 7; SOL IN ALKALINE AQ SOLN
FREELY SOL IN DIMETHYLFORMAMIDE & DIMETHYL SULFOXIDE; SLIGHTLY SOL IN METHANOL & PYRIDINE; PRACTICALLY INSOL IN ETHER, BENZENE, & CHLOROFORM
3.98e-01 g/L
>44.4 [ug/mL] (The mean of the results at pH 7.4)
Breast Feeding; Lactation; Milk, Human; Antihypertensive Agents; Thiazide Diuretics
FDA approved drugs -> Active ingredient
FDA approved drugs -> Active ingredient
Antihypertensive medicines
안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.
Danger
H317 (99.7%): May cause an allergic skin reaction [Warning Sensitization, Skin]
P233, P260, P261, P271, P272, P280, P284, P302+P352, P304+P340, P321, P333+P317, P342+P316, P362+P364, P403, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 344 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
SYMPTOMS: Symptoms of exposure to this compound may include skin and mucous membrane irritation; pancreatitis, depression of the formed elements of the blood; purpura, photosensitive dermatitis, necrotizing vasculitis, hyperglycemia, aggravation of diabetes mellitus; exacerbation of renal and/or hepatic insufficiency; lethargy, potassium loss, hyperglycemia, hyperuricemia, coma, chloride loss, lethargy, muscle cramps, acidosis, skin rash, salivary gland obstruction, psychosis, convulsions, leukopenia, jaundice, excessive amount of calcium in the blood, acute glomerulonephritis, anorexia, nausea, vomiting, cramping, diarrhea, dizziness, constipation, vertigo, paresthesis, headache, xanthopsia, hemolytic anemia, urticuria, fever, respiratory distress, including pneumonitis and pulmonary edema, anaphylactic reactions, glycosuria, muscle spasm, weakness, transient blurred vision and restlessness.
Manufacturers, packers, and distributors of drug and drug products for human use are responsible for complying with the labeling, certification, and usage requirements as prescribed by the Federal Food, Drug, and Cosmetic Act, as amended (secs 201-902, 52 Stat. 1040 et seq., as amended; 21 U.S.C. 321-392).
C - Cardiovascular system
QC - Cardiovascular system
Like other thiazides, chlorothiazide promotes water loss from the body (diuretics). It inhibits Na<sup>+</sup>/Cl<sup>-</sup> reabsorption from the distal convoluted tubules in the kidneys. Thiazides also cause loss of potassium and an increase in serum uric acid. Thiazides are often used to treat hypertension, but their hypotensive effects are not necessarily due to their diuretic activity. Thiazides have been shown to prevent hypertension-related morbidity and mortality although the mechanism is not fully understood. Thiazides cause vasodilation by activating calcium-activated potassium channels (large conductance) in vascular smooth muscles and inhibiting various carbonic anhydrases in vascular tissue. Chlorothiazide affects the distal renal tubular mechanism of electrolyte reabsorption. At maximal therapeutic dosages, all thiazides are approximately equal in their diuretic efficacy. Chlorothiazide increases excretion of sodium and chloride in approximately equivalent amounts. Natriuresis may be accompanied by some loss of potassium and bicarbonate. After oral doses, 10-15 percent of the dose is excreted unchanged in the urine. Chlorothiazide crosses the placental but not the blood-brain barrier and is excreted in breast milk.
As a diuretic, chlorothiazide inhibits active chloride reabsorption at the early distal tubule via the Na-Cl cotransporter, resulting in an increase in the excretion of sodium, chloride, and water. Thiazides like chlorothiazide also inhibit sodium ion transport across the renal tubular epithelium through binding to the thiazide sensitive sodium-chloride transporter. This results in an increase in potassium excretion via the sodium-potassium exchange mechanism. The antihypertensive mechanism of chlorothiazide is less well understood although it may be mediated through its action on carbonic anhydrases in the smooth muscle or through its action on the large-conductance calcium-activated potassium (KCa) channel, also found in the smooth muscle.
THE MECHANISM BY WHICH THIAZIDE DIURETICS LOWER BLOOD PRESSURE HAS NOT BEEN FIRMLY ESTABLISHED. /THIAZIDE DIURETICS/
현재 필터 조건에 해당하는 반응 기록이 없습니다.
불러오는 중…
648 to 649 °F (Decomposes) (NTP, 1992)
342.5-343
Decomposes at 342.5-343 °C
350 °C
Crystals; white powder. (NTP, 1992)
Solid
6.85
pKa1 = 6.85; pKa2 = 9.45
Off-White Solid
EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.
SMALL SPILLS AND LEAKAGE: If you spill this chemical, FIRST REMOVE ALL SOURCES OF IGNITION, then dampen the solid spill material with toluene, then transfer the dampened material to a suitable container. Use absorbent paper dampened with toluene to pick up any remaining material. Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal. Solvent-wash all contaminated surfaces with toluene followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.
SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)
...IN DOG PRELOADED WITH SODIUM BICARBONATE, URINE EXCRETED AFTER ADMIN OF A THIAZIDE CONTAINS RELATIVELY MORE BICARBONATE THAN CHLORIDE. /BENZOTHIADIAZIDES/
USE OF ENTERIC-COATED COMBINATIONS OF POTASSIUM CHLORIDE & THIAZIDE... ASSOCIATED WITH A HIGH INCIDENCE OF ULCERATION OF DISTAL JEJUNUM OF ILEUM. /BENZOTHIADIAZIDES/
Concurrent use of thiazide diuretics with amiodarone may lead to an increased risk of arrhythmias associated with hypokalemia. /Thiazide diuretics/
Effects /of coumarin- or indandione-derivative anticoagulants/ may be decreased when used concurrently with thiazide diuretics as a result of reduction of plasma volume leading to concentration of procoagulant factors in the blood; in addition, diuretic-induced improvement of hepatic function resulting in increased procoagulant factor synthesis; dosage adjustments may be necessary. /Thiazide diuretics/
For more Interactions (Complete) data for CHLOROTHIAZIDE (16 total), please visit the HSDB record page.
TWO SMALL CHILDREN...INGESTED TOTAL DOSE OF 15 G CHLOROTHIAZIDE BETWEEN THEM, PRESENTED WITH LETHARGY WHICH PROGRESSED TO DEEP COMA WITHIN 12 HR. BOTH RECOVERED WITHOUT SEQUELAE, & NEITHER CHILDREN EXHIBITED OBJECTIVE EVIDENCE OF FLUID OR ELECTROLYTE DISORDER. ...22-MO-OLD CHILD WHO INGESTED 3 G EXHIBITED LETHARGY.
FETAL OR NEONATAL EFFECT IS THROMBOCYTOPENIA. /FROM TABLE/
Maternal and fetal deaths in two cases of acute hemorrhagic pancreatitis were attributed to the use of chlorothiazide in the second and third trimesters.
In addition to diuresis and resultant dehydration, overdosage of thiazides may produce lethargy, nausea, weakness, and electrolyte imbalance; lethargy may progress to coma within a few hours with minimal depression of respiratory and cardiovascular function and without evidence of dehydration or serum electryolye change. The mechanism of thiazide-induced CNS depression is unknown. GI irritation and hypermotility may occur, and temporary elevation of the BUN has been reported. Serum electrolyte changes (e.g., hypokalemia, hypochloremia, hyponatremia) may occur, especially in patients with impaired renal function. /Thiazides/
May suppress lactation, but compatible /SRP: with breast feeding/. /Thiazide diuretics, from table/
Drug Induced Liver Injury Rank (DILIrank 2.0)
Chlorothiazide
vLess-DILI-concern
2
Adverse reactions
DOI:10.1016/j.drudis.2016.02.015
DOSES OF UP TO 5 G/KG /IN MONKEYS/ BY GAVAGE PRODUCED ONLY A TRANSIENT LETHARGY OF A MODERATE DEGREE.
HYPOCHLOREMIA HAS OCCURRED IN SOME DOGS WITH INCR BICARBONATE RETENTION & ALKALOSIS.
LD50Rat oral 10 g/kg
LD50 Rat ip 1386 mg/kg
LD50 Rat iv 200 mg/kg
LD50 Mouse oral 8 g/kg
For more Non-Human Toxicity Values (Complete) data for CHLOROTHIAZIDE (7 total), please visit the HSDB record page.
Chlorothiazide
11.7
49.3
The usual adult dosage is 0.5 g to 1 g once or twice a day.
Data used to generate the benchmarks include the following: Lowest Daily Dose (LDD): 500 mg/day, Lowest Therapeutic Dose (LTD): 6.3 mg/kg-day, and Screening Dose: 0.002 mg/kg-day.
21-Jan-20
Manufacturers, packers, and distributors of drug and drug products for human use are responsible for complying with the labeling, certification, and usage requirements as prescribed by the Federal Food, Drug, and Cosmetic Act, as amended (secs 201-902, 52 Stat. 1040 et seq., as amended; 21 U.S.C. 321-392).
...INDICATED THAT BENZOTHIADIAZIDES HAVE A DIRECT EFFECT ON RENAL TUBULAR TRANSPORT OF SODIUM & CHLORIDE INDEPENDENT OF CARBONIC ANHYDRASE INACTIVATION. /THIADIAZIDES/
IRRESPECTIVE OR ULTIMATE MECHANISM, IT APPEARS THAT DIURETIC THIAZIDES RELAX PERIPHERAL ARTERIOLAR SMOOTH MUSCLE. /THIAZIDES/
CARBONIC ANHYDRASE INHIBITOR WITHOUT EXCESSIVE BICARBONATE EXCRETION WITH RESULTANT ACIDOSIS.
For more Mechanism of Action (Complete) data for CHLOROTHIAZIDE (10 total), please visit the HSDB record page.
45-120 minutes
Half-life is 1.5 hours. /From Table/
Chlorothiazide is not metabolized but is eliminated rapidly by the kidney.
...CHLOROTHIAZIDE...METABOLICALLY STABLE & FOLLOWING IV ADMIN TO...HUMANS...EXCRETED UNCHANGED IN URINE.
77W477J15H
CHLOROTHIAZIDE
Physiologic Effects [PE] - Increased Diuresis
Established Pharmacologic Class [EPC] - Thiazide Diuretic
Chemical Structure [CS] - Thiazides
Chlorothiazide is a Thiazide Diuretic. The physiologic effect of chlorothiazide is by means of Increased Diuresis.
Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS.
Agents that promote the excretion of urine through their effects on kidney function.
Agents that inhibit SODIUM CHLORIDE SYMPORTERS. They act as DIURETICS. Excess use is associated with HYPOKALEMIA.
Rapidly absorbed following oral administration.
Chlorothiazide is not metabolized but is eliminated rapidly by the kidney. After oral doses, 10 to 15 percent of the dose is excreted unchanged in the urine. Chlorothiazide crosses the placental but not the blood-brain barrier and is excreted in breast milk.
CHLOROTHIAZIDE IS DISTRIBUTED THROUGHOUT EXTRACELLULAR SPACE & DOES NOT ACCUMULATE IN TISSUES OTHER THAN THE KIDNEY.
ALL OF THE THIAZIDE-LIKE DRUGS CROSS THROUGH THE PLACENTA.
IN NEPHRECTOMIZED ANIMAL, CHLOROTHIAZIDE MAY BE EXCRETED IN THE BILE; IT DOES NOT UNDERGO METABOLIC ALTERATION.
CHLOROTHIAZIDE IN A 1.1 FETAL/MATERNAL CONCN RATIO REQUIRES 60 MIN TO APPEAR IN FETUS... /FROM TABLE/
Diuretic /sodium salt/
MEDICATION (VET):
(1975) 7.5X10+6 GRAMS (PRINCPL CUSTMS DISTS)
(1976) 1.73X10+7 GRAMS (PRINCPL CUSTMS DISTS)
(1972) GREATER THAN 4.54X10+5 GRAMS
(1975) 4.54X10+5 GRAMS
REACTION OF 3-CHLOROANILINE WITH CHLOROSULFONIC ACID FOLLOWED BY TREATMENT WITH AMMONIA TO GIVE 3-CHLORO-4,6-DISULFONAMIDOANILINE WHICH IS THEN HEATED WITH FORMIC ACID
NOVELLO, SPRAGUE, J AM CHEM SOC 79, 2058 (1957); NOVELLO, HINKLEY, US PATENTS 2,809,194; 2,937,169 (1957, 1960, BOTH TO MERCK & CO).
Pharmaceuticals -> Diuretics -> Transformation products
Pharmaceuticals -> Animal Drugs -> Approved in Taiwan
2H-1,2,4-Benzothiadiazine-7-sulfonamide, 6-chloro-, 1,1-dioxide: ACTIVE
A 3 DAY TREATMENT WITHDRAWAL PERIOD SHOULD BE OBSERVED TO AVOID UNTOWARD EFFECTS IN PEOPLE FROM CONSUMING MEAT & ESPECIALLY MILK FROM TREATED ANIMALS.
개요Chlorothiazide is a first-in-class thiazide diuretic initially discovered from its ability to inhibit carbonic anhydrase in vitro. As an antihypertensive agent, this thiazide increases renal excretion of sodium, potassium, chloride, and bicarbonate ions by inhibiting tubular reabsorptive mechanisms.
용도Chlorthiazide is a diuretic that causes the body to excrete excess fluid. This drug exhibits strong diuretic action during both acidosis and alkalosis. It is used for arterial hypertension, in edematous syndromes of various genesis, congestive effects in cardiovascular insufficiency, nephrosis and nephritis, and toxicosis. It is especially recommended for hypertonic illnesses. It lowers intraocular pressure in a number of cases.
일반 설명Crystals; white powder.
정의ChEBI: Chlorothiazide is 4H-1,2,4-benzothiadiazine 1,1-dioxide in which the hydrogen at position is substituted by chlorine and that at position 7 is substituted by a sulfonamide group. A diuretic, it is used for treatment of oedema and hypertension. It has a role as a diuretic and an antihypertensive agent.