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10H-3,10a-Epidithiopyrazino[1,2-a]indole-1,4-dione, 2,3,5a,6-tetrahydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-, [3R-(3alpha,5abeta,6beta,10aalpha)]-

HCID 3477
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
67-99-2
Standard SMILES
CN1C(=O)C23CC4=CC=CC(O)C4N2C(=O)C1(CO)SS3
InChIKey
FIVPIPIDMRVLAY-UHFFFAOYSA-N
Molecular formula
C13H14N2O4S2
Average molar mass
326.4 g/mol
Monoisotopic mass
326.03949928

Overview

gliotoxin has been reported in Aspergillus fumigatus with data available.

Names & identifiers

Preferred name
10H-3,10a-Epidithiopyrazino[1,2-a]indole-1,4-dione, 2,3,5a,6-tetrahydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-, [3R-(3alpha,5abeta,6beta,10aalpha)]-
IUPAC
7-hydroxy-11-(hydroxymethyl)-15-methyl-12,13-dithia-9,15-diazatetracyclo[9.2.2.01,9.03,8]pentadeca-3,5-diene-10,14-dione
English name
GLIOTOXIN
Molecular formula
C13H14N2O4S2
Molecular weight
326.39

Names & synonyms

NSC 102866CHEMBL1972524SCHEMBL14986985BCBcMAP01_000033FIVPIPIDMRVLAY-UHFFFAOYSA-NNSC77672NSC 77672NSC-77672SMP1_000141NCI60_000081S-82SN 12870
Show more names
GLIOTOXINs.n.12870Nsc102866Aids086418aspergillinAids-086418Gliotoxin solutionAspergillin solutionGliotoxin in Acetonitrile
S. N. 1287010H-3,10a-Epidithiopyrazino(1,2-a)indole-1,4-dione,2,3,5a,6-tetrahydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-10H-3,10a-Epidithiopyrazino[1,2-a]indole-1,4-dione, 2,3,5a,6-tetrahydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-, [3R-(3.alpha.,5a.beta.,6.beta.,10a.alpha.)]-10H-3,2-a]indole-1,4-dione, 2,3,5a,6-tetrahydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-, [3R-(3.alpha.,5a.beta.,6.beta.,10a.alpha.)]-10H-3,2-a]indole-1,4-dione, 2,3,5a,6-tetrahydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-,(3R,5aS,6S,10aR)-

Database identifiers

CAS
67-99-2

Properties

Computed structural properties

XLogP
-0.7
Topological polar surface area
132 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
6
Rotatable bonds
1
Heavy atoms
21
Formal charge
0
Complexity
621

Physicochemical properties

Melting point
221 °C · 221°C (rough estimate)
Boiling point
699.7 · 699.7±55.0 °C(Predicted)
alpha
25 · D25 -290° (c = 0.08 in ethanol)
Density
1.4069 · 1.4069 (rough estimate)
refractive index
1.651 · 1.6510 (estimate)
Flash point
2 ℃ · 2℃
storage temp.
2 · 2-8°C
solubility
10 mg/mL, · chloroform: 10 mg/mL, clear, colorless
form
White solid
pka
12.9 · 12.90±0.40(Predicted)
color
Monoclinic crystals from MeOH
Merck
13 · 13,4454
BRN
50675 · 50675
Stability
2 yeara · Stable for 2 yeara as supplied. Solutions in DMSO may be stored at -20°C for up to 1 month.
InChI
InChI=1S/C13H14N2O4S2/c1-14-10(18)12-5-7-3-2-4-8(17)9(7)15(12)11(19)13(14,6-16)21-20-12/h2-4,8-9,16-17H,5-6H2,1H3/t8-,9-,12+,13+/m0/s1

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

F
4.2-10-23
wgk
3
rtecs
KB4725000
ridadr
UN 3462 6.1/PG 3
hs_code
29419090
Toxicity
LD50 oral in mouse: 67mg/kg
risk_code
25-36-20/21/22-11
Signal word
Danger
Symbol(GHS)
GHS06
hazard_code
T,Xn,F
safety_code
36/37/39-45-36/37-16
hazard_class
6.1(b)
Storage Class
6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
packing_group
III
Hazard statements
H301
Hazard Classifications
Acute Tox. 3 Oral
Precautionary statements
P301+P310

Chemistry & industry

Applications · 3 items

DescriptionGliotoxin is an immunosuppressive mycotoxin produced by pathogenic strains of Aspergillus and other fungi with diverse biological activities. It inhibits 20S proteasomal chymotrypsin activity (IC50 = 10 μM), blocking the degradation of IκBα and preventing the activation of NF-κB. Gliotoxin induces apoptosis in monocytes and dendritic cells and reduces phagocytosis by neutrophils. It suppresses viral infection by Nipah and Hendra virus in HEK293T cells (IC50s = 149 and 579 nM, respectively). Under reducing conditions, gliotoxin inhibits leukotriene A4 hydrolase (LTA4H; ) epoxide hydrolase activity, but not aminopeptidase activity, and leukotriene B4 (LTB4; ) synthesis in neutrophils and monocytes. In vivo, gliotoxin (5 mg/kg) reduces LTB4 plasma levels and blocks peritoneal neutrophil infiltration in a mouse model of peritonitis induced by zymosan A . It also inhibits geranylgeranyltransferase I and farnesyltransferase (IC50s = 17 and 80 μM, respectively).

UsesGliotoxin is a sulfur-containing mycotoxin produced by species of fungi and pathogens of humans. Gliotoxin exhibits inhibitory activities against histone H3K9 methyltransferase, a key enzyme in the re gulation of transcriptional activity by writing epigenetic marks. Gliotoxin also exhibits immunosuppressive properties by causing apoptosis of cells of the immune system. In addition, various studies suggests Gliotoxin may also be a potential anti-inflammatory, antibiotic, antifungal and antiviral agent.

UsesGliotoxin is a potent epithiodioxopiperazine mycotoxin produced by species of Gliocladium, Aspergillus and Penicillium. At the cellular level gliotoxin inhibits a broad range of unrelated mechanisms, including inhibition of chymotrypsin-like activity of the 20S proteasome and Ca2+ release from mitochondria, activation of transcription factor NF-κB in response to a variety of stimuli in T and B cells, anti-inflammatory activity, and inhibition of farnesyltransferase and geranylgeranyltransferase. The mode of action appears to be via covalent interaction with proteins through mixed disulphide formation. Gliotoxin inhibits a number of thiol-requiring enzymes and also displays antioxidant and immunomodulatory activity.

Upstream & downstream products

Downstream products

(3R)-2,3,5aβ,6α-Tetrahydro-6β-hydroxy-3β-(hydroxymethyl)-2-methyl-10H-3α,10aα-epitetrathiopyrazino[1,2-a]indole-1,4-dione

Related reactions

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New reaction record

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
PubChem CID
3477
ChEMBL
CHEMBL1972524
InChIKey
FIVPIPIDMRVLAY-RBJBARPLSA-N
SMILES
N12C(=O)[C@@]3(CO)SS[C@@]1(C(=O)N3C)CC1[C@@]2([H])[C@@H](O)C=CC=1
FDA UNII
5 L648PH06K · 5L648PH06K
UNSPSC Code
12352200 · 12352200
Symbol(GHS)
6 · GHS06
Signal word
Danger
Hazard statements
301 · H301
Precautionary statements
301 · P301+P310
Hazard Codes
T,Xn,F
Risk Statements
25 · 25-36-20/21/22-11
Safety Statements
36 · 36/37/39-45-36/37-16
RIDADR
3462 · UN 3462 6.1/PG 3
WGK Germany
3 · 3
RTECS
4725000 · KB4725000
F
4.2 · 4.2-10-23
HazardClass
6.1 · 6.1(b)
PackingGroup
III
HS Code
29419090 · 29419090
Storage Class
6.1 C · 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
Hazard Classifications
3 Oral · Acute Tox. 3 Oral
Toxicity
50 oral · LD50 oral in mouse: 67mg/kg
Bis(methylthio)gliotoxin

Suppliers83 total

南京世洲生物科技有限公司025-85560043 15850508050 · [email protected]
成都普瑞法科技开发有限公司+86-028-82633397 18982077548 · [email protected]
湖北永阔科技有限公司027-59223108 15972152991 · [email protected]
成都乐美天医药科技有限公司17308096051 17308096051 · [email protected]
成都超九八生物科技有限公司13348960310 13348960310 · [email protected]
艾吉析科技(上海)有限公司17717235263 · [email protected]
上海纯优生物科技有限公司15921393123 18302135232 · [email protected]
成都埃法生物科技有限公司028-028-85142057 19983342022 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
河南赢创生物科技有限公司16650615803 · [email protected]
Shaanxi Cuikang Pharmaceutical Technology Co., Ltd+86-13119157289 · [email protected]
武汉众志诚生物技术有限公司13628624121 13628604890 · [email protected]
上海赛可锐生物科技有限公司021-58000709 13120558703 · [email protected]
湖北丹鼎医药科技有限公司18917019315(微信同号) 17701422019 · [email protected]
武汉易泰科技有限公司上海分公司18930552037 · [email protected]
上海颖心实验室设备有限公司021-59178156 17002132182 · [email protected]
安耐吉化学&3A(安徽泽升科技有限公司)021-58432009 400-005-6266 · [email protected]
孟成科技(上海)有限公司400-820-6829 · [email protected]
梯希爱(上海)化工贸易有限公司021-61109150 · [email protected]
上海诗丹德标准技术服务有限公司021-021-57127007-6622-6622 17621252073 · [email protected]
銳迪國際科技有限公司18024082417 · [email protected]
上海维亦特生物科技有限公司15317051735 · [email protected]
武汉市皇臻生物化工有限公司13795480948 · [email protected]
云南西力生物技术股份有限公司0871-65217109 · [email protected]
金克隆(北京)生物技术有限公司400-910-1997 15330005590 · [email protected]
AdooQ BioScience, LLC+1 (866) 930-6790 · [email protected]
成都麦德生科技有限公司028-82253651 18140204969 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
杭州杰恒化工有限公司0571-87396432 · [email protected]
上海永叶生物科技有限公司86-021-61559134 15921386130 · [email protected]
陕西缔都医药化工有限公司+86-29-87569262 +86-15003564040 · [email protected]
凯试(上海)科技有限公司021-50135380 · [email protected]
Sigma-Aldrich西格玛奥德里奇(上海)贸易有限公司021-61415566 800-8193336 · [email protected]
天津阿尔塔科技有限公司022-6537-8550 15522853686 · [email protected]
四川精萃天成药物科技有限公司028-87865381 18108190480 · [email protected]
浙江珲达生物科技有限公司0571-89903022 18679456698 · [email protected]
EMMX Biotechnology LLC888-539-0666 · [email protected]
上海一飞生物科技有限公司021-65675885 18964387627 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
湖北齐飞医药化工有限公司027-59322506 18071128681 · [email protected]
青岛贞开生物医药技术有限公司0532-58268781 18561687109 · [email protected]
上海澄绍生物科技有限公司021-61847300 13341622919 · [email protected]
上海超岚化工科技中心(原上海巢莱)0-2022843681 15618226720 · [email protected]
西安莱茵生物科技有限公司86-(0)29-85992781 17792393971 · [email protected]
Novachemistry44-20819178-90 02081917890 · [email protected]
南京尚书生物科技有限公司18266960953 · [email protected]
陕西缔都医药化工有限公司029-81154043 17391733319 · [email protected]
Shanghai Acmec Biochemical Technology Co., Ltd.+86-18621343501 · [email protected]
上海研生实业有限公司021-59989018 15201736385 · [email protected]
毕升化学(上海)有限公司19852830193 19852830193 · [email protected]

Additional notes

DefinitionChEBI: A pyrazinoindole with a disulfide bridge spanning a dioxo-substituted pyrazine ring; mycotoxin produced by several species of fungi.