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모닐리포르민

Moniliformin

HCID 40452
노트반응
기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
31876-38-7
표준 SMILES
O=c1cc(O)c1=O
InChIKey
KGPQKNJSZNXOPV-UHFFFAOYSA-N
분자식
C4H2O3
평균 분자량
98.06 g/mol
단동위원소 질량
98.00039392

이름 및 식별자

우선 이름
Moniliformin
IUPAC
3-hydroxycyclobut-3-ene-1,2-dione
현지명
모닐리포르민
영어명
moniliformin
분자식
C4H2O3
분자량
98.06

이름 및 동의어

Moniliformin31876-38-73-hydroxycyclobut-3-ene-1,2-dioneSemisquaric acid3-Cyclobutene-1,2-dione, 3-hydroxy-1-Hydroxycyclobut-1-ene-3,4-dioneHydroxycyclobutenedione3-Hydroxy-3-cyclobutene-1,2-dione3-Hydroxy-3-cyclobutenedioneG5JMQ8SDF81-Hydroxy-cyclobut-1-ene-3,4-dioneDTXSID10185731
이름 더 보기
모닐리포르민
RefChem:159498DTXCID50108222636-113-2981-476-51-hydroxycyclobutene-3,4-dioneNSC2928961345994-72-039284-13-4

데이터베이스 식별자

CAS
31876-38-7、71376-34-6
PubChem CID
40452
DTXSID
DTXSID10185731
ChEMBL
CHEMBL1977616
ChEBI
CHEBI:222613
UNII
G5JMQ8SDF8
EC Number
636-113-2、981-476-5
Nikkaji
J20.107C

물성

구조 계산 물성

XLogP
-0.6
극성 표면적
54.4 Ų
수소 결합 공여자 수
1
수소 결합 수용자 수
3
회전 가능 결합 수
0
무거운 원자 수
7
형식 전하
0
복잡도
166

물리화학적 성질

녹는점
163 °C · 163°C (rough estimate)
끓는 점
123.51 °C · 123.51°C (rough estimate)
밀도
1.3154 · 1.3154 (rough estimate)
굴절률
1.454 · 1.4540 (estimate)
산도 계수 (pKa)
-0.21 · -0.21±0.25(Predicted)

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

GHS 분류

GHS Classification · 6건

Danger

H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]

P264, P270, P301+P316, P321, P330, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 41 reports by companies from 2 notifications to the ECHA C&L Inventory.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.

유해성 정보

Regulatory InformationRegulation (EC) No 178/2002 (amended)
Hazard Classes and Categories · 2건

Acute Tox. 3 (100%)

Acute Tox. 2 (100%);Skin Irrit. 2 (100%);Eye Irrit. 2A (100%);STOT SE 3 (100%)

독성 정보

TreatmentKashin-Beck disease cannot be cured but can be treated with physical therapy and corrective surgery. Natamycin ophthalmic suspension is the drug of choice for filamentous fungal infections such as mycotic keratitis. (L1964, L1828)
Health Effects · 1건

Moniliformin is believed to be a cause of Kashin-Beck disease, which causes joint destruction and deformity. It may also have immunosuppressive properties and can cause fungal infections such as mycotic keratitis. (A3021, A3075, A3076, L1970)

Exposure RoutesOral, dermal, inhalation, and parenteral (contaminated drugs). (A3101)
Toxicity Summary

화학 및 산업

용도 및 제조

UsesMoniliformin is a mycotoxin produced by a number of fungi of the Fusarium species. It can by found in contaminated cereal crops. (L1969, A3075)

응용 분야

용도Moniliformin is a toxic secondary metabolite ofFusarium spp..

상·하류 제품 정보

상류 원료

디클로로케텐3-Cyclobutene-1,2-dione, 3-chloro-4-hydroxy-2-Cyclobuten-1-one, 2,3,4-tris(1,1-dimethylethoxy)-Cyclobutanone, 2,2,3,3-tetraethoxy-Cyclobutene, 1,4-dichloro-3,3,4-trifluoro-2,3-di-tert-butoxy-4-hydroxy-2-cyclobuten-1-oneTetramethoxyethylene케텐에틸비닐에테르

관련 반응

1건
반응 기록 만들기
HRID 372627 반응식
HRID 372627반응물로uspto-grants-1978_05

화합물 노트

불러오는 중…

이 페이지에서기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
· 1건

Moniliformin reversibly inhibits the enzymes pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase by competing for the binding site of pyruvate. This interferes with the tricarboxylic acid cycle by preventing the necessary incorporation of pyruvate and oxidation of the alpha-ketoglutarate intermediate. Moniliformin has also been shown to interfere with carbohydrate metabolism by inhibiting transketolase and aldose reductase. Moniliformin causes the necrosis of human chondrocytes in cartilage. It does so by increasing the expression of matrix catabolic enzymes, such as MMP-1 and MMP-13, and decreasing the syntheses of extracellular matrix components such as aggrecan and type II collage. This accelerates the catabolism of the extracellular matrix in articular cartilages, inducing a loss of cartilage function and eventually leading to cartilage degradation. Moniliformin is also known to cause DNA damage, inducing chromatid breaks, chromosome breaks, and chromatid exchanges. (A3075, A3076, A3077)

Signs and Symptoms · 1건

The main symptoms of acute moniliformin toxication in animals are muscular weakness, respiratory stress, myocardial degeneration, as well as some histopathological changes in organs such as the kidneys, the lungs and the pancreas, followed by coma and death. Kashin-Beck disease is characterized by joint pain, with restriction of movement and joint enlargement. (A3077)

Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).

규제 정보

Regulatory InformationRegulation (EC) No 178/2002 (amended)