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HCID 2082생성일: 2026년 10월 26일

[5-(프로필시오)-1H-벤지마이다졸-2-일]카르바믹산 메틸 에스테르; 알벤다졸

[5-(프로필시오)-1H-벤지마이다졸-2-일]카르바믹산메틸에스테르 · 알벤다졸 · Albendazol · S-oxide · Methyl (6-(propylthio)-1H-benzo[d]imidazol-2-yl)carbamate · ALBEN · ZENTEL · Atasol

https://huagongshe.com/ko/chemical/2082

[5-(프로필시오)-1H-벤지마이다졸-2-일]카르바믹산 메틸 에스테르; 알벤다졸 분자 구조식

식별자 및 물리적 특성

CAS No.54965-21-8
분자식C12H15N3O2S
평균 분자량265.33 g/mol
단동위원소 질량265.08849772 g/mol
SMILESCCCSc1ccc2nc(NC(=O)OC)[nH]c2c1
InChIKeyHXHWSAZORRCQMX-UHFFFAOYSA-N
PubChem CID2082
ChEMBLCHEMBL1483
ChEBICHEBI:16664
EC No.259-414-7
DTXSIDDTXSID0022563
현지명[5-(프로필시오)-1H-벤지마이다졸-2-일]카르바믹산 메틸 에스테르; 알벤다졸

화학 및 물리적 성질

XLogP2.9
극성 표면적92.3
수소 결합 공여자 수2
수소 결합 수용자 수4
회전 가능 결합 수5
무거운 원자 수18
형식 전하0
복잡도290
의약품PharmaceuticalsPharmaceuticals -> Listed in ZINC15
LogP(분배 계수)log Kow = 1.272.73.24
Color/FormColorless crystals
용해도Practically insoluble2.28e-02 g/L1.4 [ug/mL] (The mean of the results at pH 7.4)물에 거의 녹지 않으며, 무수 포름산에 잘 녹고, 염화메틸렌에 아주 약간 녹고, 에탄올(96%)에는 거의 녹지 않습니다.
Human DrugsBreast FeedingLactationMilk, HumanAnti-Infective AgentsAnticestodal AgentsAntiparasitic AgentsAntiprotozoal AgentsFDA approved drugs -> Active ingredientPharmaceuticalsAntifilarials
Animal DrugsActive Ingredients (Albendazole) -> FDA GreenbookPharmaceuticals -> UK Veterinary Medicines Directorate List
녹는점208-210208-210 °CMol wt: 281.34. Active metabolite of albendazole. MP: 226-228 °C (decomposes) /Sulfoxide/209 °C
Physical DescriptionSolid
Collision Cross Section160.4 Ų [M]+ [CCS Type: DTBuffer gas: N2Ionization: APCI+Dataset: TOXCASTSource Identifier: DTXSID0022563]166.6 Ų [M+H]+ [CCS Type: TWMethod: calibrated with Waters Major Mix]172.57 Ų [M+Na]+ [CCS Type: TWMethod: calibrated with polyalanine and drug standards]162 Ų [M+H]+ [CCS Type: TW
밀도1.2561 (rough estimate)
굴절률1.6740 (estimate)
저장 조건2-8°C
pKa(산도 계수)10.72±0.10(Predicted)
물리적 상태Solid
색상흰색에서 황백색까지
용해도0.75mg/L(209℃)
Merck14,210
헨리 상수1.3×108 mol/(m3Pa) at 25℃, HSDB (2015)
BCS Class4
주요 응용법의학 및 독성학의약품(소분자)
InChIInChI=1S/C12H15N3O2S/c1-3-6-18-8-4-5-9-10(7-8)14-11(13-9)15-12(16)17-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)
InChIKeyHXHWSAZORRCQMX-UHFFFAOYSA-N
SMILESC(OC)(=O)NC1NC2=CC(SCCC)=CC=C2N=1

화학적 성질

Albendazole occurs as a white to faintly yellowish powder. It is practically insoluble in water and alcohol, very slightly soluble in ether and dichloromethane, but freely soluble in anhydrous formic acid.

안전 및 규제

GHS 분류This chemical does not meet GHS hazard criteria for 3.4% (5 of 149) of reports.DangerH315 (20.1%): Causes skin irritation [Warning Skin corrosion/irritation]P203, P260, P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P318, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 149 reports by companies from 22 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
규제 정보Albendazole: Does not have an individual approval but may be used under an appropriate group standard
기타 안전 정보IMAP assessments - Carbamic acid, [5-(propylthio)-1H-benzimidazol-2-yl]-, methyl ester: Human health tier I assessment
FDA 요건The Approved Drug Products with Therapeutic Equivalence Evaluations List identifies currently marketed prescription drug products, incl albendazole, approved on the basis of safety and effectiveness by FDA under sections 505 of the Federal Food, Drug, and Cosmetic Act.Oral dosage form new animal drugs. Albendazole suspension. ... Conditions of use in cattle: Indications for use: Indications for use. For removal and control of the following internal parasites of cattle: Adult liver flukes (Fasciola hepatica)heads and segments of tapeworms (Moniezia benedeni, M. expansa)adult and 4th stage larvae of stomach worms (brown stomach worms including 4th stage inhibited larvae (Ostertagia ostertagi), barberpole worm (Haemonchus contortus, H. placei), small stomach worm (Trichostrongylus axei))adult and 4th stage larvae of intestinal worms (thread-necked intestinal worm (Nematodirus spathiger, N. helvetianus), small intestinal worm (Cooperia punctata and C. oncophora))adult stages of intestinal worms (hookworm (Bunostomum phlebotomum), bankrupt worm (Trichostrongylus colubriformis), nodular worm (Oesophagostomum radiatum))adult and 4th stage larvae of lungworms (Dictyocaulus viviparus). ... Conditions of use in sheep: For removal and control of the following internal parasites of sheep: Adult liver flukes (Fasciola hepatica, Fascioloides magna)heads and segments of common tapeworms (Moniezia expansa) and fringed tapeworm (Thysanosoma actinioides)adult and fourth stage larvae of stomach worms (brown stomach worm (Ostertagia circumcinta and Marshallagia marshalli), barberpole worm (Haemonchus contortus), small stomach worm (Trichostrongylus axei))adult and fourth stage larvae of intestinal worms (thread-necked intestinal worm (Nematodirus spathiger and N. filicollis), Cooper's worm (Cooperia oncophora), bankrupt worm (Trichostrongylus colubriformis), nodular worm (Oesophagostomum columbianum), and large-mouth bowel worm (Chabertia ovina))adult and larval stages of lungworms (Dictyocaulus filaria).Oral dosage form new animal drugs. Albendazole paste. ... Conditions of use in cattle: For removal and control of the following internal parasites of cattle: adult liver flukes (Fasciola hepatica)adult and 4th stage larvae of stomach worms (brown stomach worms including 4th stage inhibited larvae (Ostertagia ostertagi)barberpole worm (Haemonchus contortus, H. placei)small stomach worm (Trichostrongylus axei))adult and 4th stages larvae of intestinal worms (thread-necked intestinal worm (Nematodirus spathiger, N. helvetianus)small intestinal worm (Cooperia punctata and C. oncophora))adult stages of intestinal worms (hookworm (Bunostomum phlebotmum)bankrupt worm (Trichostrongylus colubriformis), nodular worm (Oesophagostomum radiatum))adult and 4th stage larvae of lungworms (Dictyocaulus viviparus).Tolerances - (1) Cattle. A tolerance is established for albendazole 2-aminosulfone (marker residue) in liver (target tissue) of 0.2 part per million and in muscle of 0.05 part per million. (2) Sheep. A tolerance is established for albendazole 2-aminosulfone (marker residue) in liver (target tissue) of 0.25 part per million and in muscle of 0.05 part per million.The Generic Animal Drug and Patent Restoration act requires that each sponsor of an approved animal drug must submit to the FDA certain information regarding patents held for the animal drug or its method of use. The Act requires that this information, as well as a list of all animal drug products approved for safety and effectiveness, be made available to the public. Albendazole is included on this list.
Special ReportsDayan ADPreparing to control Schistosomiasis and Soil-transmitted Helminthiasis in the Twenty-First CenturyActa Tropica 86 (2-3): 141-159 (2003)
Hazard Classes and CategoriesSkin Irrit. 2 (20.1%)
처리 방법SRP: 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.
Allowable TolerancesTolerances-(1) Cattle. A tolerance is established for albendazole 2-aminosulfone (marker residue) in liver (target tissue) of 0.2 part per million and in muscle of 0.05 part per million. (2) Sheep. A tolerance is established for albendazole 2-aminosulfone (marker residue) in liver (target tissue) of 0.25 part per million and in muscle of 0.05 part per million.
상호 작용Regimens in which albendazole with either ivermectin or diethylcarbamazine are given as single annual doses show great promise for controlling lymphatic filariasis occurring either alone or together with other filarial infections. Such combined therapy has the additional benefit of reducing intestinal roundworm infections in school-aged children.... Plasma levels of /albendazole's/ sulfoxide metabolites can be increased by coadministration of glucocorticoids and possibly praziquantel.
HepatotoxicityAlbendazole therapy has been associated with transient and asymptomatic elevations in serum aminotransferase levels in up to 50% of patients treated for more than a few weeks. These abnormalities rapidly improve with stopping therapy which is rarely required (~4%). Albendazole has also been associated with rare instances of clinically apparent liver injury. The onset of injury has been within a few days to as long as 2 months of starting therapy or more rapidly with multiple courses of treatment. The injury can also arise 1 to 2 weeks after a short course of albendazole (1 to 3 days). The pattern of serum enzyme elevations is typically hepatocellular or mixed. Allergic features (rash, fever, eosinophilia) may be present but are not prominent. Most cases have been mild to moderate in severity, and recovery is distinctively rapid once the drug is stopped. However, severe and even fatal cases of albendazole induced liver injury have been reported. Rapid recurrence with rechallenge has been reported but with similar severity. Cases with acute liver failure leading to emergency liver transplantation or death have also occurred.
환경 거동TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 120(SRC), determined from a log Kow of 1.27(2) and a regression-derived equation(3), indicates that albendazole is expected to have high mobility in soil(SRC). Volatilization of albendazole from moist soil surfaces is not expected to be an important fate process(SRC) based on an estimated Henry's Law constant of the neutral species is 7.6X10-14 atm-cu m/mole(SRC), determined using a fragment constant estimation method(4). Albendazole is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 1.5X10-9 mm Hg(SRC), determined from a fragment constant method(5). Biodegradation data were not available(SRC, 2006).AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 120(SRC), determined from a log Kow of 1.27(2) and a regression-derived equation(3), indicates that albendazole is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 7.6X10-14 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), an estimated BCF of 5(SRC), from its log Kow(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Based on an estimated rate constant of 2.6X10-4 L/mole-sec(7), half-lives for the hydrolysis of albendazole at pH 7 and 8 are 840 and 84 years, respectively. Measured half-lives for the direct photolysis of albendazole in sunlit water at pH 5,7, and 9 are 10, 16, and 6 minutes, respectively, under summer conditions and 50, 80, and 20 minutes, respectively, under winter conditions(8,9). Biodegradation data were not available(SRC, 2006).ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), albendazole, which has an estimated vapor pressure of 1.5X10-9 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely in the particulate phase in the ambient atmosphere. Particulate-phase albendazole may be removed from the air by wet or dry deposition(SRC). Albendazole is expected to undergo direct photolysis based on measured half-lives in sunlit waters at pH 5, 7, and 9 of 10, 16, and 6 minutes, respectively, under summer conditions and 50, 80, and 20 minutes, respectively, under winter conditions(3,4).
유해 작용The most common adverse effects accompanying albendazole use are headaches and elevated liver enzymes, with 10% to 20% of patients experiencing elevated liver enzymes. Some other side effects of albendazole include abdominal pain, nausea, vomiting, and fever. A small percentage of patients may experience a hypersensitivity reaction to the drug, such as hives and pruritus. There are reports of alopecia and telogen effluvium in the literature as rare side effects of albendazole therapy. Fortunately, alopecia and telogen effluvium usually reverse after completing the treatment.
노출 경로Poorly absorbed from the gastrointestinal tract due to its low aqueous solubility. Oral bioavailability appears to be enhanced when coadministered with a fatty meal (estimated fat content 40 g)
독성 요약Albendazole's low solubility prevents it from being absorbed in large enough quantities to be toxic to humans. There is no specific antidote for albendazole overdose.Albendazole causes degenerative alterations in the tegument and intestinal cells of the worm by binding to the colchicine-sensitive site of tubulin, thus inhibiting its polymerization or assembly into microtubules. The loss of the cytoplasmic microtubules leads to impaired uptake of glucose by the larval and adult stages of the susceptible parasites, and depletes their glycogen stores. Degenerative changes in the endoplasmic reticulum, the mitochondria of the germinal layer, and the subsequent release of lysosomes result in decreased production of adenosine triphosphate (ATP), which is the energy required for the survival of the helminth. Due to diminished energy production, the parasite is immobilized and eventually dies.
Signs and SymptomsSymptoms of overdose include elevated liver enzymes, headaches, hair loss, low levels of white blood cells (neutropenia), fever, and itching.
Soil Adsorption/MobilityThe Koc of albendazole is estimated as 120(SRC), using a log Kow of 1.27(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that albendazole is expected to have high mobility in soil.
Human Toxicity Excerpts/SIGNS AND SYMPTOMS/ ... Adverse effects include fever, reversible leucopenia, headache, nausea, dizziness, sleeplessness, epigastric pain and diarrhoea./CASE REPORTS/ Albendazole is a benzimidazole with wide spectrum coverage as an antiparasitic drug. Reported side effects have been minimal. ... The case of a patient who died with severe prolonged pancytopenia beginning during the third week of therapy for a pulmonary echinococcal cyst /is reported/. This case was a 68-year-old man who presented with a large cystic lung mass. His medical history was significant for Child-Pugh class B cirrhosis. A prolonged course of albendazole was initiated. Two weeks later, the patient presented in septic shock with severe pancytopenia. The patient was initially resuscitated, but died after 10 days with no marrow recovery. Autopsy was consistent with albendazole-induced pancytopenia. This is the third human case of pancytopenia and the first death reported in relation to albendazole-induced pancytopenia. Neutropenia seems to be related more to higher dosage and longer duration of use. Albendazole sulfoxide peak dose and half life are significantly prolonged by liver disease and concomitant administration of certain drugs. The severity and duration of albendazole-induced pancytopenia in this case was likely related to the underlying liver disease. Frequent serial monitoring of blood counts and cessation of medication with any evidence of marrow toxicity in such patients is warranted./OTHER TOXICITY INFORMATION/ Albendazole at 10 to 12 mg/kg/day has been given continuously for 3 to 6 mo without producing serious or irreversible toxicity.
Artificial Pollution SourcesAlbendazole's production and use as an anthelmintic drug in humans and animals(1,2) may result in its release to the environment through various waste streams(SRC).
Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).
Drug Induced Liver InjuryDrug Induced Liver Injury Rank (DILIrank 2.0)AlbendazolevMost-DILI-concern7Warnings & precautionsDOI:10.1016/j.drudis.2016.02.015
수질 위해 등급(WGK)2
RTECS 번호FD1100000
관세 코드29332990
위험 문구(R)61-36/37/38-48/22-63-33
위험 표시T,Xn
안전 문구(S)53-45-37/39-26-36/37-24/25
기존화학 물질KE-29862
위험 등급Aquatic Acute 1Aquatic Chronic 1Repr. 2STOT RE 2 Oral
저장 분류11 - Combustible Solids
유해 물질 데이터54965-21-8(Hazardous Substances Data)

용도

용도

알벤다졸(albendazole, albendazolum)은 다양한 기생충 감염을 치료하기 위해 사용되는 약물이다. 편모충증, 편충증, 필라리아병, 신경낭미충증, 포충증, 요충증, 회충증 등에 유용하다.

용도

Albendazole is a derivative of benzimidazole, is a drug with a broad antihelmintic spectrum. It exhibits an antihelmintic effect against sensitive cestodes and nematodes by blocking the process of glucose uptake by the parasites, which is expressed in the depletion of glycogen reserves and subsequent reduction in the level of adenosintriphophate. As a result, the parasite stops moving and dies. It is used upon infection of Acaris lumbricoides, Ancylostoma duodenale, Necator americanus, Enterobius vermicularis, and Trichuris trichiura. Synonyms of this drug are SKF 62979 and others.

일반 설명

Albendazole occurs as a white crystalline powder that isvirtually insoluble in water. The oral absorption of albendazoleis enhanced by a fatty meal. The drug undergoes rapidand extensive first-pass metabolism to the sulfoxide, whichis the active form in plasma. The elimination half-life ofthe sulfoxide ranges from 10 to 15 hours. Considerable biliaryexcretion and enterohepatic recycling of albendazolesulfoxide occurs. Albendazole is generally well toleratedin single-dose therapy for intestinal nematodes. The highdose,prolonged therapy required for clonorchiasis orechinococcal disease therapy can result in adverse effectssuch as bone marrow depression, elevation of hepatic enzymes,and alopecia.