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팔로인

Phalloin

HCID 34183
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
28227-92-1
표준 SMILES
CC1NC(=O)C(CC(C)(C)O)NC(=O)C2Cc3c([nH]c4ccccc34)SCC(NC(=O)C(C(C)O)NC1=O)C(=O)N1CC(O)CC1C(=O)NC(C)C(=O)N2
InChIKey
VVAHMTWEOWYEHQ-UHFFFAOYSA-N
분자식
C35H48N8O10S
평균 분자량
772.9 g/mol
단동위원소 질량
772.32141074

개요

phalloin has been reported in Amanita phalloides, Amanita bisporigera, and other organisms with data available.

이름 및 식별자

우선 이름
Phalloin
IUPAC
18-hydroxy-34-(1-hydroxyethyl)-28-(2-hydroxy-2-methylpropyl)-23,31-dimethyl-12-thia-10,16,22,25,27,30,33,36-octazapentacyclo[12.11.11.03,11.04,9.016,20]hexatriaconta-3(11),4,6,8-tetraene-15,21,24,26,29,32,35-heptone
현지명
팔로인
영어명
phalloin
분자식
C35H48N8O10S
분자량
772.87

이름 및 동의어

PHALLOIN28227-92-1DTXSID40104631818-hydroxy-34-(1-hydroxyethyl)-28-(2-hydroxy-2-methylpropyl)-23,31-dimethyl-12-thia-10,16,22,25,27,30,33,36-octazapentacyclo[12.11.11.03,11.04,9.016,20]hexatriaconta-3(11),4,6,8-tetraene-15,21,24,26,29,32,35-heptone18-hydroxy-34-(1-hydroxyethyl)-28-(2-hydroxy-2-methylpropyl)-23,31-dimethyl-12-thia-10,16,22,25,27,30,33,36-octazapentacyclo(12.11.11.03,11.04,9.016,20)hexatriaconta-3(11),4,6,8-tetraene-15,21,24,26,29,32,35-heptoneRefChem:860501DTXCID70152814718,21,24,26,29,32,35-heptahydroxy-28-(2-hydroxy-2-methylpropyl)-34-(1-hydroxyethyl)-23,31-dimethyl-12-thia-10,16,22,25,27,30,33,36-octaazapentacyclo(12.11.11.03,11.04,9.016,20)hexatriaconta-3(11),4,6,8,21,24,26,29,32,35-decaen-15-onePhalloineHSDB 3525Phalloidin, 7-(4-hydroxy-L-leucine)-SCHEMBL30682996
이름 더 보기
팔로인Phalloin (6CI,7CI,8CI,9CI)Cyclo(L-Ala-D-Thr-L-Cys(1)-L-c4Hyp-L-Ala-L-Trp2(1)-4-hydroxy-L-Leu-)
NS00126146Q9257868

물성

구조 계산 물성

XLogP
-0.6
극성 표면적
297 Ų
수소 결합 공여자 수
10
수소 결합 수용자 수
11
회전 가능 결합 수
3
무거운 원자 수
54
형식 전하
0
복잡도
1,480

실험 및 물리화학적 성질

Chemical ClassesBiological Agents -> Mushroom Toxins

물리화학적 성질

끓는 점
1314.6 · 1314.6±65.0 °C(Predicted)
밀도
1.1492 · 1.1492 (rough estimate)
굴절률
1.74 · 1.7400 (estimate)
산도 계수 (pKa)
13.04 · 13.04±0.70(Predicted)

안전 및 규제

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

유해성 정보

Hazards Summary · 1건

Phalloin and gamma-amanitin were detected within the 1st day and phalloidin within the 2nd day in the urine of rats after the administration of amanita phalloides extracts. [HSDB] Intraperitoneal LD50 (mouse) = 1 mg/kg; [RTECS] See Phalloidin.

Special Reports · 1건

THE HISTORY OF TOXIC COMPONENTS MAY BE DIVIDED INTO 2 PERIODS. THE 1ST STUDIES BEGAN IN THE LATE 18TH CENTURY AND RESULTED IN DISTINGUISHING BETWEEN NON-TOXIC HEMOLYSIN OR PHALLINE, AND A POORLY DEFINED TOXIC COMPOUND. THE 2ND PERIOD BEGAN WITH THE ISOLATION OF PHALLOIDINE IN 1937, FOLLOWED BY ISOLATION OF ALPHA, BETA AND GAMMA AMANITINE AND PHALLOINE. CLASSIFICATION, STRUCTURE, CONCENTRATIONS, TOXICITY IN ANIMALS AND STRUCTURE-ACTIVITY RELATIONSHIPS ARE DISCUSSED FOR THESE. ALSO REVIEWED ARE DATA ON SYNTHESIS OF TOXIN CONSTITUENTS, RESEARCH ON THE ANTITOXIN, ANTAMANIDE.[THEVENIN M ET AL; AMANITA PHALLOIDES AND ITS TOXINS: I. REVIEW OF RESEARCH ON THE IDENTITY OF THE TOXIC COMPONENTS; EUR J TOXICOL ENVIRON HYG 9(4) 197 (1976)]

독성 정보

TreatmentConsider gastric lavage and activated charcoal. (A678)
Health EffectsLiver lesions, tachycardia, hypoglycemia, hypotension and electrolyte imbalance with acid- base disturbance (L1160).
Adverse EffectsNeurotoxin - Other CNS neurotoxin
Exposure RoutesOral, dermal, inhalation, and parenteral (contaminated drugs). (A3101)
Toxicity Summary · 1건

Phallotoxins bind actin, preventing its depolymerization and poisoning the cell. They bind specifically at the interface between F-actin subunits, locking adjacent subunits together. This leads to a decrease in the rate constant for the dissociation of actin subunits from filament ends, which essentially stabilizes actin filaments through the prevention of filament depolymerization. Moreover, they inhibit the ATP hydrolysis activity of F-actin. (L1183, A2465)

화학 및 산업

약리 정보

Metabolism/MetabolitesPHALLOIN AND GAMMA-AMANITIN WERE DETECTED WITHIN THE 1ST DAY AND PHALLOIDIN WITHIN THE 2ND DAY IN THE URINE OF RATS AFTER THE ADMINISTRATION OF AMANITA PHALLOIDES EXTRACTS.

용도 및 제조

Uses · 2건

Oligopeptide similar to phalloidin. [ChemIDplus]

Prophalloin is one of a group of toxins from the death cap (Amanita phalloides) known as phallotoxins. (L996)

Methods of Manufacturing · 1건

COUPLING OF THE S-CHLORIDE OF BOC TERT-BUTYLOXYCARBONYL-ALANYL-D-THREONYL-CYSTEINYL-ALLO-HYDROXYPROLINE WITH ALANYL-TRYPTOPHYL-GAMMA-HYDROXYLEUCINE LACTONE GAVE A THIOETHER, WHICH ON CYCLIZATION YIELDED BOC-SECOPHALLOIN LACTONE. REMOVAL OF THE BOC RESIDUE, OPENING OF THE LACTONE RING AND A 2ND CYCLIZATION LED TO PHALLOIN, WHICH PROVED IDENTICAL WITH THE NATURAL TOXIN IN PHYSICAL AND TOXICOLOGICAL RESPECTS.

관련 반응

0건
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화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트

데이터베이스 식별자

CAS
28227-92-1
PubChem CID
34183
DTXSID
DTXSID401046318
Signs and Symptoms · 1건

Hypovolemic shock; Gastrointestinal symptoms occur after a latent period and include abdominal pain, vomiting, and watery diarrhea. Neurologic symptoms are related to hepatic failure and may include encephalopathy, somnolence, confusion, coma and seizures (L1160).

Human Toxicity Excerpts · 3건

THE MOST SERIOUS FORM OF MYCETISMUS IS PRODUCED BY GALERINA SPECIES, AMANITA VERNA, AMANITA VIROSA, AND AMANITA PHALLOIDES, WHICH ARE FAIRLY COMMON IN BOTH NORTH AMERICA AND EUROPE. THESE SPECIES ACCOUNT FOR 90% OF ALL FATAL CASES. THE PRINCIPAL TOXINS ARE THE PHALLOIDINS, A GROUP OF CYCLIC HEPTAPEPTIDES THAT APPEAR TO INHIBIT PROTEIN SYNTHESIS, AND THE AMANITINS, WHICH INHIBIT RNA POLYMERASE II AND HENCE INTERFERE WITH THE SYNTHESIS OF MESSENGER RNA. THE TOXINS DISRUPT HEPATIC CELL MEMBRANES AND THE STRUCTURE OF THE ENDOPLASMIC RETICULUM. /PHALLOIDINS/

THE PHALLOTOXINS ARE SOMETIMES SAID TO BE RESPONSIBLE FOR...INITIAL GASTROENTERITIS /OF MUSHROOM POISONING/... /PHALLOTOXINS/

THE PHALLOTOXINS (WHICH INCLUDE PHALLOIDIN) POSSESS A COMMON CYCLIC HEPTAPEPTIDE SKELETON WITH SOME UNUSUAL AMINO ACIDS. AT LEAST IN THE CASE OF PHALLOIDIN, WHICH MAY OR MAY NOT HAVE TO BE ALTERED CHEMICALLY BY THE LIVER BEFORE IT ACQUIRES ITS CHARACTERISTIC ABILITY TO INJURE THAT ORGAN, CYTOTOXICITY IS ASSOCIATED WITH A THIOETHER LINKAGE BETWEEN CYSTEINE AND TRYPTOPHAN IN THE TOXIN MOLECULE.

Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).
Toxicity DataLD50: 1.5 mg/kg (Mouse) (T258)

안전 데이터

독성
LD50 ipr-mus: 1 mg/kg NEJMAG 269,223,63
유해 물질 데이터
28227-92-1(Hazardous Substances Data)