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HCID 4649생성일: 2026년 10월 26일

4-아미노살리실 산

4-아미노살리실산 · 4-아미노살리실릭애씨드 · 4-아미노살리실릭애씨드및그염류 · PAS · 4-AMINO-2-HYDROXYBENZOIC ACID · AMINOSALICYLIC ACID · Pasa · 4-Asa

https://huagongshe.com/ko/chemical/4649

4-아미노살리실 산 분자 구조식

식별자 및 물리적 특성

CAS No.65-49-6
분자식C7H7NO3
평균 분자량153.14 g/mol
단동위원소 질량153.04259308 g/mol
SMILESNc1ccc(C(=O)O)c(O)c1
InChIKeyWUBBRNOQWQTFEX-UHFFFAOYSA-N
PubChem CID4649
ChEMBLCHEMBL1169
ChEBICHEBI:27565
EC No.200-613-5
DTXSIDDTXSID2022591
현지명4-아미노살리실 산

화학 및 물리적 성질

XLogP1.3
극성 표면적83.6
수소 결합 공여자 수3
수소 결합 수용자 수4
회전 가능 결합 수1
무거운 원자 수11
형식 전하0
복잡도160
물질 분류Nitrogen Compounds -> Aminobenzoic Acids
의약품Pharmaceuticals -> AntibioticsPharmaceuticals -> Listed in ZINC15
pHPH (SATURATED AQ SOLN): BETWEEN 3 & 3.73.5 (1g/l, H2O, 20℃)
SpringerMaterials PropertiesDiamagnetic susceptibility
LogP(분배 계수)LogP= 1.321.6
냄새ODORLESS, OR HAS SLIGHT ACETOUS ODOR
Color/FormMINUTE CRYSTALS FROM ALCWHITE, OR NEARLY WHITE, BULKY POWDERNEEDLES, PLATES FROM ALC-ETHERA reddish-brown crystalline powder is obtained on recrystallization from ethanol-ether.
용해도1 G SOL IN ABOUT 7 ML WATERSLIGHTLY SOL IN ALC /CALCIUM SALT/PH OF 1% SOLN: ABOUT 7FREELY SOL IN WATER /POTASSIUM SALT/For more Solubility (Complete) data for P-AMINOSALICYLIC ACID (7 total), please visit the HSDB record page.SOL IN DILUTE NITRIC ACID & DILUTE SODIUM HYDROXIDEVirtually insoluble in benzene, choroform, or carbon tetrachloride1.69g/L
Human DrugsBreast FeedingLactationMilk, HumanAnti-infective AgentsAntitubercular AgentsFDA approved drugs -> Active ingredient
녹는점150-151 °C, with effervescenceNEEDLES FROM ALCMP: 115 °C /ETHYL ESTER/150.5 °C135-145 °C (lit.)
증기압0.000004 [mmHg]
Physical DescriptionWhite or nearly white solidAffected by light and air[Hawley] Beige powder[MSDSonline]
끓는 점276.03°C (rough estimate)
밀도1.3585 (rough estimate)
굴절률1.5500 (estimate)
저장 조건Keep in dark place,Inert atmosphere,Room temperature
물리적 상태가루
pKa(산도 계수)3.25(at 25℃)
색상무색의
용해도2g/L(20℃)
Merck14,477
BRN473071
Specific Activity17.6-26.4nmol/min·mg
BCS Class4/2
안정성흡습성
주요 응용펩타이드 합성
InChI1S/C7H7NO3/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,9H,8H2,(H,10,11)
InChIKeyWUBBRNOQWQTFEX-UHFFFAOYSA-N
SMILESNc1ccc(C(O)=O)c(O)c1
NISTAminosalicylic acid(65-49-6)
EPA4-Aminosalicylic acid (65-49-6)

화학적 성질

beige powder

안전 및 규제

GHS 분류WarningH315 (43.5%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, 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 69 reports by companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
규제 정보Status: Active Update: 23-11-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/25234Benzoic acid, 4-amino-2-hydroxy-: Does not have an individual approval but may be used under an appropriate group standard
기타 안전 정보IMAP assessments - Benzoic acid, 4-amino-2-hydroxy-: Environment tier I assessment
유해성 요약Not expected to increase congenital malformations based on animal studies[REPROTOX] Oral LD50 (mouse) = 4000 mg/kg[RTECS] An eye irritantTargets the GI system and liver[MSDSonline] See p-Aminosalicylic acid sodium salt dihydrate.
FDA 요건Manufacturers, 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 amended21 U.S.C. 321-392).
Special ReportsA review of the literature on the clinical experience, tolerance and toxicity of mesalamine (5-aminosalicylic acid), aminosalicylic acid (4-aminosalicylic acid) and newer mesalamine based drugs for the treatment of chronic inflammatory bowel disease is presented.[Jarnerot GDrugs 37 (Jan): 73-86 (1989)]The initial therapy and retreatment of pulmonary tuberculosis as well as various complicating factors that may affect treatment decisions are presented. Chemotherapeutic agents used in the treatment of tuberculosis and their dosage regiments are mentioned including isoniazid, ethambutol, rifampin, pyrazinamide, ethionamide, cycloserine, streptomycin, kanamycin, aminosalicylate (aminosalicylic acid), and capreomycin.[Spagnolo SVDrug Therapy 15 (Nov): 91-92, 97-100 (1985)]
Hazard Classes and CategoriesSkin Irrit. 2 (43.5%)
보관 조건Store below 90 °C (104 °F), unless otherwise specified by manufacturer. Store in tight, light resistant containers.
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.
상호 작용...PARA-AMINOSALICYLIC ACID.../INHIBITS METABOLISM OF CHLORAMPHENICOL/PENTOBARBITAL /SRP: CNS DEPRESSION/ IN MICE WAS ENHANCED AFTER PRE-TREATMENT WITH... P-AMINOSALICYLIC ACID. INCR /SRP: CNS DEPRESSION/ APPEARED TO BE DUE TO RELEASE OF PENTOBARBITAL FROM SERUM-PROTEIN BINDING, RESULTING IN HIGHER CEREBRAL CONCN...ADDITIVE & SYNERGISTIC WITH STREPTOMYCINS & ISONIAZID.Probenecid decreases the renal excretion of this agent.For more Interactions (Complete) data for P-AMINOSALICYLIC ACID (19 total), please visit the HSDB record page.
유해 작용Occupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
Human Toxicity ExcerptsSEVERE THERAPEUTIC MISADVENTURES, ALTHOUGH RARE, HAVE INCL...HEPATITIS...METHEMOGLOBINEMIA...Adequate and well-controlled studies in humans have not been done. In one study, an increased malformation rate for ears and limbs, and hypospadias were reported in infants of patients taking aminosalicylates with other antitubercular medications. However, other studies have not found aminosalicylates to be teratogenic. /Aminosalicylates/The literature has been reviewed for contact dermatitis occurring to antituberculosis agents. Of the 12 known drugs, 6 (isoniazid, rifampicin, ethambutol, p-aminosalicylic acid, streptomycin and kanamycin) have been documented by patch test to cause this type of dermatitis in certain individuals.
Drug Induced Liver InjuryDrug Induced Liver Injury Rank (DILIrank 2.0)Aminosalicylic acidvMOST-DILI-concern5Warnings & precautionsDOI:10.1016/j.drudis.2016.02.015
Non-Human Toxicity ExcerptsAn N-acetylation polymorphism is described that is expressed toward arylamine carcinogens in tumor target organs of an inbred rat model. High levels ... of arylamine carcinogen N-acetyltransferase activity were observed in kidney, colon, prostate and urinary bladder cytosols derived from Fischer (F-344) inbred rats ... Significantly lower ... levels of arylamine carcinogen N-acetyltransferase activity were observed for corresponding tissue cytosols derived from Wistar-Kyoto inbred rats. Intermediate levels of arylamine carcinogen N-acetyltransferase activity significantly different from both the parental strains were observed in F1 hybrids of the parental strains, consistent with codominant expression of two alleles at a single gene locus. The arylamine substrates exhibiting the acetylator phenotype-dependent N-acetyltransferase activities included ... p-aminosalicylic acid ... Highest levels of arylamine carcinogen N-acetyltransferase were expressed consistently in colon cytosol, but expression of the N-acetylation polymorphism toward arylamine carcinogens was observed in each (kidney, colon, prostate and urinary bladder) of the tumor target organs. The expression of the N-acetylation polymorphism in tumor target organs suggests that the inbred rat model will be useful in assessing the role of acetylator phenotype in arylamine-induced cancers of the colon and prostate.An overview is presented of a selected number of mono-aromatic derivatives and their short-term effects on hepatic fatty acid biosynthesis. The cmpd discussed in this paper are o-hydroxybenzoate ... m-hydroxybenzoate, p-hydroxybenzoate, benzoate, p-t-butylbenzoate, p-aminosalicylate, clofibrate, halofenate, alpha-cyano-4-hydroxycinnamate and benfluorex. All of these drugs inhibit fatty acid biosynthesis by isolated rat liver cells, albeit with different effectiveness. In contrast, the cmpd have differential effects on fatty acid esterification and oxidation by isolated hepatocytes. An attempt is made to describe in molecular terms the underlying mechanisms of the acute inhibitory effects of the mono-aromatic derivatives on hepatic lipogenesis. It is proposed that all of the drugs exert an inhibitory action at the level of acetyl-CoA carboxylase, the enzyme generally considered to catalyze the rate-limiting step in hepatic fatty acid synthesis. This inhibitory effect may be either direct, i.e. by an alteration of the enzyme's structure as a results of interaction between drug and enzyme, or indirect, i.e. through a drug-induced change in the cellular levels of allosteric effectors of acetyl-CoA carboxylase.
Effects During Pregnancy and Lactation◉ Summary of Use during Lactation
수질 위해 등급(WGK)2
TSCA 등재 상태TSCA listed
RTECS 번호VO1225000
운송 번호(UN)UN 1789 8/PG 3
독성LD50 orally in mice: 4 g/kg (Bavin)
관세 코드29225000
위험 문구(R)22-36-36/37/38-45-35-61
위험 표시Xn,Xi,T
안전 문구(S)26-37/39-45-53-36-36/37/39
기존화학 물질KE-01389
저장 분류11 - Combustible Solids
유해 물질 데이터65-49-6(Hazardous Substances Data)

용도

용도

antimycobacterial antitubercular;NF-kB inhibitor.4-Aminosalicylic acid (p-aminosalicylic acid, PAS), an antituberculosis drug, is a model active pharmaceutical ingredient to study salt and cocrystal formation in a multiple hydrogen-bonding functionality molecule with carboxylic acid, amine, and phenol groups.It has also been used as a second line agent to sulfasalazine in people with inflammatory bowel disease such as ulcerative colitis and Crohn's disease.It is typically taken by mouth.

일반 설명

4-Aminosalicylic acid occurs as a white to yellowish white crystalline solid that darkens on exposure to light or air. It is slightly soluble in water but more soluble in alcohol. Alkali metal salts and the nitric acid salt are soluble in water, but the salts of hydrochloric acid and sulfuric acid are not. The acid undergoes decarboxylation when heated. An aqueous solution has a pH of approximately 3.2. PAS is administered orally in the form of the sodium salt, usually in tablet or capsule form. Symptoms of gastrointestinal irritation are common with both the acid and the sodium salt. Various enteric-coated dosage forms have been used in an attempt to overcome this disadvantage. Other forms that are claimed to improve gastrointestinal tolerance include the calcium salt, the phenyl ester, and a combination with an anion exchange resin (Rezi-PAS). An antacid such as aluminum hydroxide is frequently prescribed. The oral absorption of PAS is rapid and nearly complete, and it is widely distributed into most of the body fluids and tissues, with the exception of the CSF, in which levels are significantly lower.It is excreted primarily in the urine as both unchanged drug and metabolites.