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Swainsonine

HCID 51683
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
72741-87-8
표준 SMILES
O[C@H]1[C@H]2[C@H](O)CCCN2C[C@H]1O
InChIKey
FXUAIOOAOAVCGD-WCTZXXKLSA-N
분자식
C8H15NO3
평균 분자량
173.21 g/mol
단동위원소 질량
173.10519334

개요

Swainsonine is an indolizidine alkaloid isolated from the plant Swainsona canescens with three hydroxy substituents at positions 1, 2 and 8. It has a role as an antineoplastic agent, an immunological adjuvant, an EC 3.2.1.114 (mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase) inhibitor and a plant metabolite.

이름 및 식별자

우선 이름
Swainsonine
IUPAC
(1S,2R,8R,8aR)-1,2,3,5,6,7,8,8a-octahydroindolizine-1,2,8-triol
영어명
SWAINSONINE
분자식
C8H15NO3
분자량
173.21

이름 및 동의어

swainsonine72741-87-8TridolgosirDTXSID5046356(1S,2R,8R,8aR)-Octahydro-1,2,8-indolizinetriolRSY4RK37KQ(1S,2R,8R,8aR)-1,2,3,5,6,7,8,8a-octahydroindolizine-1,2,8-triol1,2,8-Indolizinetriol, octahydro-, (1S-(1alpha,2alpha,8beta,8abeta))-CHEBI:9367DTXCID3026356tridolgosirumRefChem:890073
이름 더 보기
8AR)-1SwainMoiaD-SwainsonineSWAINSONINE 98+%(-)-D-SwainsonineSwainsonine min. 99%swainsonine synthetic
(-)-SwainsonineTridolgosir [INN]Swainsonine (Synthetic)MFCD00017554(1S,2R,8R,8aR)-octahydroindolizine-1,2,8-triol1S-8AB-OCTAHYDRO-INDOLIZIDINE-1A,2A,8B-TRIOLCHEMBL371197NCGC00163481-02

데이터베이스 식별자

CAS
72741-87-8
PubChem CID
51683
DTXSID
DTXSID5046356
ChEMBL
CHEMBL371197

물성

구조 계산 물성

XLogP
-1.3
극성 표면적
63.9 Ų
수소 결합 공여자 수
3
수소 결합 수용자 수
4
회전 가능 결합 수
0
무거운 원자 수
12
형식 전하
0
복잡도
176

실험 및 물리화학적 성질

DrugsPharmaceuticals -> Listed in ZINC15
Melting Point143-144 °C

물리화학적 성질

녹는점
148 · 148-149°C
끓는 점
353.3 · 353.3±21.0 °C(Predicted)
밀도
1.38 · 1.38±0.1 g/cm3 (20 ºC 760 Torr)
저장 조건
-20 °C · -20°C
용해도
2 O: · H2O: 용해성1mg/mL
물리적 상태
동결건조된 분말
산도 계수 (pKa)
14.01 · 14.01±0.60(Predicted)
색상
흰색에서 희미한 노란색까지
생물학적 소스
synthetic
수용성
50 mM까지 · 물에 50mM까지 용해됨
BRN
4175740 · 4175740
안정성
1 · 제공된 대로 구매일로부터 1년 동안 안정적입니다. DMSO, 에탄올 또는 증류수에 용해된 용액은 -20°C에서 최대 3개월 동안 보관할 수 있습니다.
InChI
1S/C8H15NO3/c10-5-2-1-3-9-4-6(11)8(12)7(5)9/h5-8,10-12H,1-4H2/t5-,6-,7,8-/m1/s1
InChIKey
FXUAIOOAOAVCGD-DCDLSZRSSA-N

안전 및 규제

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

GHS 분류

GHS Classification · 4건

Warning

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P270, P271, P280, P301+P317, P302+P352, P304+P340, P317, P321, P330, P362+P364, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

유해성 정보

Hazard Classes and CategoriesAcute Tox. 4 (100%)

독성 정보

Health Effects · 2건

The presence of phytotoxins in plants constitutes a health risk for herbivores, particularly on ruminants who accidently consume them. Among the adverse effects produced by these exposures are reproductive alterations, represented by abortion, infertility, and morphological alterations in neonates, which are frequently attributed to other causes. While in some cases the plants that contain such metabolites are known, other times they are not, leading to alterations that are difficult to treat considering that their toxicodynamics are unknown.

Swainsonine causes a variety of neurological disorders, including locoism and "slobbers syndrome" in livestock. In man it causes a lysosomal storage disease, biochemically and morphologically similar to mannosidosis. It is also an appetite suppressant. (L1248, A3092, A3093)

Exposure RoutesOral, dermal, inhalation, and parenteral (contaminated drugs). (A3101)
Toxicity Summary · 1건

Swainsonine inhibits the activity of glycoside hydrolases, especially N-linked glycosylation. Inhibition of Golgi mannosidase II and other alpha-mannosidases causes the accumulation of atypical hybrid glycoproteins and oligosaccarides because the proper processing cannot occur. This also results in intracellular vacuolization. (L1248, A3092, A3093)

화학 및 산업

약리 정보

Mechanism of Action · 2건

Tridolgosir competitively inhibits the alpha manosidase II (alphaMII), which processes N linked carbohydrates of newly synthesized glycoproteins passing through the Golgi apparatus to the cell surface. Highly branched carbohydrate structures are created which bind to Lectin-phytohemagglutinin (L-PHA) and are subsequently expressed in different tumor types which results in metastatic phenotype, which is correlated with an increased aggressiveness in animals and causes other human malignancies. Inhibition of alphaMII reduces carbohydrates that bind to L-PHA, reducing aggressiveness, metastatic phenotype cells, slows tumor growth, and increases“hybrid type” carbohydrates on the cell surface. Hybrid type carbohydrates may increase cytokine activation of lymphocytes, increasing tumor susceptibility to lymphokine activated and natural killer cells.

Locoweed contains the indolizidine alkaloid swainsonine. Livestock that consume locoweed can suffer from locoism. The toxic component in locoweed has been identified as swainsonine. Swainsonine inhibits lysosomal a-mannosidase and mannosidase II, resulting in altered oligosaccharide degradation and incomplete glycoprotein processing. Endophytic fungi producing swainsonine have been isolated from a variety of locoweed, and these fungi and locoweed have a close relationship, e.g., endophytic fungi can promote the growth of locoweed and increase swainsonine production. Livestock that consume locoweed exhibit several symptoms, including dispirited behavior, staggering gait, chromatopsia, trembling, ataxia, and cellular vacuolar degeneration of most tissues.

MeSH Pharmacological Classification · 3건

Substances that augment, stimulate, activate, potentiate, or modulate the immune response at either the cellular or humoral level. The classical agents (Freund's adjuvant, BCG, Corynebacterium parvum, et al.) contain bacterial antigens. Some are endogenous (e.g., histamine, interferon, transfer factor, tuftsin, interleukin-1). Their mode of action is either non-specific, resulting in increased immune responsiveness to a wide variety of antigens, or antigen-specific, i.e., affecting a restricted type of immune response to a narrow group of antigens. The therapeutic efficacy of many biological response modifiers is related to their antigen-specific immunoadjuvanticity.

Agents obtained from higher plants that have demonstrable cytostatic or antineoplastic activity.

Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction.

관련 반응

9건
반응 기록 만들기
HRID 375262 반응식
HRID 375262생성물로uspto-grants-1996_01
HRID 581377 반응식
HRID 581377반응물로uspto-grants-1999_07
HRID 974167 반응식
HRID 974167반응물로uspto-grants-1991_11
HRID 981550 반응식
HRID 981550반응물로uspto-grants-1991_02
HRID 1494207 반응식
HRID 1494207반응물로uspto-grants-1991_06
HRID 1494659 반응식
HRID 1494659반응물로uspto-grants-1991_06
HRID 1937438 반응식
HRID 1937438생성물로uspto-grants-2002_05
HRID 1975837 반응식
HRID 1975837생성물로uspto-grants-1994_02
1 / 2 페이지

화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
ChEBI
CHEBI:9367
UNII
RSY4RK37KQ
EC Number
615-797-6
Nikkaji
J12.698E
SMILES
O[C@@H]1CCCN2C[C@@H](O)[C@@H](O)C12

화학적 성질

White Crystalline Solid

Signs and Symptoms · 2건

Several plants that contain indolizidine alkaloids, including swainsonine, are toxic to livestock, causing dysfunctional lysosomes and storage disease. Swainsonine induces a neurovisceral disease, known as locoism, in sheep, goats, and cattle. Locoism occurs in several parts of the world, e.g., the western United States, China, and parts of Australia. In South America, locoism has been described in the Andean region of Argentina affecting sheep, cattle, and llamas. This publication describes the clinical course in llamas, which was about 15 days, and included moderate ataxia, incoordination of hindlimbs, and progressive loss of body condition. Swainsonine was detected in stem and leaf samples of A. punae at a concentration of 0.06%. A diagnosis of swainsonine toxicosis caused by the consumption of A. punae was made based on clinical history and signs, histologic and ultrastructural changes, and plant analysis.

Symptoms of locoism include staggering gait, depression, muscular incoordination, staring, nervousness, hyperexcitability, loss of appetite, and reproductive alterations such as abortion and birth defects. The major symptom of "slobbers syndrome" is profuse salivation. Other symptoms include diarrhea, lacrimation, stiff joints, frequent urination, tremors, spontaneous abortion, labored breathing, loss of appetite, bloat, and possibly death. Swainsonine also causes vacuolation of most tissues. (L1819, A3092, A3093)

Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).
Non-Human Toxicity Excerpts · 4건

Swainsonine is the primary toxin in locoweeds. It causes intention tremors, reproductive dysfunction, emaciation, and death. In a mouse study, three generations were given a range of concentrations of swainsonine by intraperitoneal injection (2.50 mg/kg body weight (BW), 1.20 mg/kg BW, 0.60 mg/kg BW, and 0 mg/kg BW). The results results indicate that swainsonine may cause reproductive and developmental toxicities in mice in both parents and offspring.

Swainsonine is the principal agent in locoweed responsible for inducing locoism in animals. The toxicity of Embellisia fungi isolated from locoweed was compared with locoweed toxicity. Rats were fed diets containing locoweed, fungus and alfalfa, or alfalfa. Similar intracellular vacuolation was observed in renal, pancreatic, and hepatic tissues of rats that consumed either locoweed or fungus. Rats that ate locoweed or Embellisia fungi displayed indistinguishable toxicity symptoms. The Embellisia fungi from locoweed can induce toxicity without the plants.

Spontaneous intoxication by Astragalus arequipensis was diagnosed in a flock of 300 sheep that grazed an area heavily invaded by this plant. The main clinical signs were intention tremors, ataxia, and progressive loss of condition. The main microscopic changes were fine cytoplasmic vacuolation of cells in the cerebrum, cerebellum, thyroid and adrenal glands, kidney, liver, pancreas, urinary bladder, and lymph nodes, and swollen axons in the cerebellum. Composite leaf and stem samples of A. arequipensis analyzed by high-performance liquid chromatography contained 0.05% swainsonine. The diagnosis of intoxication by A. arequipensis was made based on the clinical history and signs, the gross, microscopic, and ultrastructural changes, and the detection of swainsonine in the plant.

Lysosomal storage diseases can causeimpaired cellular function and death. Many acquired lysosomal storage diseases are produced by toxic plants containing indolizidine alkaloids. This includes swainsonine, which inhibits lysosomal α-mannosidase and Golgi α-mannosidase II. Swainsonine-induced nervous disease associated with various plants has been reported, including species of the genus Astragalus, Sida, Oxitropis, Swainsona, and Ipomoea. The diagnosis of Astragalus spp. intoxication is established based on clinical signs, microscopic and ultrastructural findings, lectin histochemistry, the abundance of these plants in the grazing area, and the determination of swainsonine in plant specimens.

안전 데이터

wgk
3
rtecs
NM2408666
HS 번호
29339900
risk_code
20/21/22
hazard_code
Xn
safety_code
36
스토리지 클래스
11 - Combustible Solids

용도 및 제조

UsesSwainsonine is a plant toxin found in locoweed (families Fabaceae, Oxytropis, Astragalus and Swainsona) and some fungi (Metarhizium anisopliae, Rizoctonia leguminicola). (L1248, A3092)

응용 분야

출처Swainsonia canescens yields this simple alkaloid.

일반 설명Swainsonine is produced by endophytes, plant and insect pathogens. It is synthesized from the pipecolic acid and mevalonic acid. Swainsonine is a water-soluble indole alkaloid.

공급사100 곳

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常州合晶化工有限公司85528066 13775048983 · [email protected]

추가 설명

정의ChEBI: An indolizidine alkaloid isolated from the plant Swainsona canescens with three hydroxy substituents at positions 1, 2 and 8.