HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
Huagongshe Open Program:[email protected]AI access: llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.7.8
  1. Home
  2. /Compound

T-2 Tetraol

HCID 9904331
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
34114-99-3
Standard SMILES
CC1=C[C@H]2O[C@@H]3[C@H](O)[C@@H](O)[C@](C)([C@@]2(CO)C[C@@H]1O)[C@]31CO1
InChIKey
ZAXZBJSXSOISTF-LYFQSNBGSA-N
Molecular formula
C15H22O6
Average molar mass
298.33 g/mol
Monoisotopic mass
298.14163842

Overview

T-2 Tetraol has been reported in Fusarium heterosporum, Fusarium acuminatum, and other organisms with data available.

Names & identifiers

Preferred name
T-2 Tetraol
IUPAC
(1S,2R,4S,7R,9R,10R,11S,12S)-2-(hydroxymethyl)-1,5-dimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-4,10,11-triol
English name
t-2 Tetraol
Molecular formula
C15H22O6
Molecular weight
298.33

Names & synonyms

T-2 Tetraol34114-99-3T-2 toxin tetraolZ00UFS2AP1Toxin T 2 tetraolDTXSID10893263(1S,2R,4S,7R,9R,10R,11S,12S)-2-(hydroxymethyl)-1,5-dimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-4,10,11-triolTrichothec-9-ene-3,4,8,15-tetrol, 12,13-epoxy-, (3alpha,4beta,8alpha)-(1S,2R,4S,7R,9R,10R,11S,12S)-2-(hydroxymethyl)-1,5-dimethylspiro(8-oxatricyclo(7.2.1.02,7)dodec-5-ene-12,2'-oxirane)-4,10,11-triolRefChem:890144DTXCID001323198T-2-TETRAOL
Show more names
T-4 toxinT2 Tetraot-2tetraolt-2toxintetraolT-2-Tetraol solutionT2 Tetraol 100ug/ml in ACNT-2 Tetraol in acetonitrile12,13-Epoxytrichothec-9-ene-3α,4β,8α,15-tetrol3α,4β,8α,15-Tetrahydroxy-12,13-epoxytrichothec-9-eneT-2 Tetraol Solution (50μg/ml in Acetonitrile Solution)
T-?2 Tetraol(2R,2'S,3R,4S,5S,5AR,7S,9aR)-5a-(hydroxymethyl)-5,8-dimethyl-2,3,4,5,5a,6,7,9a-octahydrospiro[2,5-methanobenzo[b]oxepine-10,2'-oxirane]-3,4,7-triol3-alpha,4-beta,8-alpha,15-Tetrahydroxy-12,13-epoxytrichothec-9-eneMFCD00078761T2 TetraolTrichothec-9-ene-3,4,8,15-tetrol, 12,13-epoxy-, (3.alpha.,4.beta.,8.alpha.)-T- 2 TetraolUNII-Z00UFS2AP1

Properties

Computed structural properties

XLogP
-2.1
Topological polar surface area
103 Ų
Hydrogen bond donors
4
Hydrogen bond acceptors
6
Rotatable bonds
1
Heavy atoms
21
Formal charge
0
Complexity
520

Physicochemical properties

Melting point
197 · 197 - 200oC
Boiling point
515.2 · 515.2±50.0 °C(Predicted)
Density
1.48 · 1.48±0.1 g/cm3(Predicted)
Flash point
6 ℃ · 6℃
storage temp.
20 °C · −20°C
solubility
Acetonitrile (Slightly), Methanol (Slightly)
form
Solid
pka
13.68 · 13.68±0.70(Predicted)
color
White to Off-White
FDA UNII
0 UFS2AP1 · Z00UFS2AP1
Symbol(GHS)
2 · GHS02,GHS07
Signal word
Danger
Hazard statements
225 · H225-H302+H312+H332-H319
Precautionary statements
210 · P210-P280-P305+P351+P338
Hazard Codes
T+,Xn,F
Risk Statements
26 · 26/27/28-36/37/38-36-20/21/22-11

Safety & regulation

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

GHS classification

GHS Classification · 4 items

Danger

H300 (100%): Fatal if swallowed [Danger Acute toxicity, oral]

P260, P261, P262, P264, P264+P265, P270, P271, P280, P284, P301+P316, P302+P352, P304+P340, P305+P351+P338, P316, P319, P320, P321, P330, P337+P317, P361+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 41 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Regulatory InformationRegulation (EC) No 178/2002 (amended)
Hazard Classes and CategoriesAcute Tox. 2 (100%)

Toxicology

Treatment · 1 item

There are no known antidotes to trichothecene mycotoxins. Treatments are directed at supporting hemopoietic abnormalities, gastrointestinal damage, and skin damage. Administer charcoal as a slurry in case of acute oral exposure. In case of inhalation: Move patient to fresh air. Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis. Administer oxygen and assist ventilation as required. Treat bronchospasm with inhaled beta2 agonist and oral or parenteral corticosteroids. In case of eye exposure, Irrigate exposed eyes with copious amounts of room temperature water for at least 15 minutes. In case of dermal exposure, Remove contaminated clothing and wash exposed area thoroughly with soap and water. (A704)

Health Effects · 1 item

Trichothecenes have multiorgan effects including anoerxia and weight loss, growth retardation, nervous disorders, cardiovascular alterations, immunodepression, hemostatic derangements, skin toxicity, decreased reproductive capacity, bone marrow damage, and alimentary toxic aleukia. (L1948, L1949, A2964)

Chemistry & industry

Pharmacology

Metabolism/Metabolites · 1 item

Trichothecenes are lipophilic and thus easily absorbed through the skin, gut, and pulmonary mucosa. They are metabolized mainly by cytochrome P-450 and trichothecene-specific carboxylesterase activity in the liver, although other tissues such as the kidney, spleen, and intestine also show some metabolic activity. Trichothecenes are metabolically transformed to less toxic metabolites by such reactions as hydrolysis, hydroxylation, de-epoxidation, and glucuronidation. Metabolites are excreted in the urine and feces. (L1910, L1949)

Uses & manufacturing

Uses · 1 item

Trichothecenes are a very large family of chemically related mycotoxins produced by various species of Fusarium, Myrothecium, Trichoderma, Trichothecium, Cephalosporium, Verticimonosporium, and Stachybotrys. They are produced on many different grains like wheat, oats or maize by various Fusarium species such as F. graminearum, F. sporotrichioides, F. poae and F. equiseti. Some molds that produce trichothecene mycotoxins, such as Stachybotrys chartarum, can grow in damp indoor environments and may contribute to health problems among building occupants. (L1948)

Applications

UsesT2 Tetraol is a type A trichothecene mycotoxin.

Suppliers27 total

阿诺西(上海)生物技术有限公司400-1107768 15058188853 · [email protected]
成都乐美天医药科技有限公司17308096051 17308096051 · [email protected]
Career Henan Chemica Co+86-0371-86658258 +86-13203830695 · [email protected]
武汉敬康恩生物医药科技有限公司

Related reactions

0 records
New reaction record

No reaction records under the current filter.

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes

Database identifiers

CAS
34114-99-3
PubChem CID
9904331
DTXSID
DTXSID10893263
ChEMBL
CHEMBL152377
UNII
Z00UFS2AP1
EC Number
621-631-3
Nikkaji
J23.685C
Safety Statements
22 · 22-36/37/39-45-36/37-16
RIDADR
2811 · UN2811 6.1/PG 1
WGK Germany
2 · 2
RTECS
9980000 · YC9980000
HS Code
38220090 · 38220090
Exposure RoutesOral, dermal, inhalation, and parenteral (contaminated drugs). (A3101)
Toxicity Summary · 1 item

Unlike many other mycotoxins, trichothecenes do not require metabolic activation to exert their biological activity, instead directly reacting with cellular components. Trichothecenes are cytotoxic to most eukaryotic cells due to their powerful ability to inhibit protein synthesis. They do this by freely moving across the plasma membrane and binding specifically to ribosomes with high-affinity. Specifically, they interfere with the active site of peptidyl transferase at the 3'-end of large 28S ribosomal RNA and inhibit the initiation, elongation or termination step of protein synthesis, as well as cause polyribosomal disaggregation. Protein synthesis is an essential function in all tissues, but tissues where cells are actively and rapidly growing and dividing are very susceptible to the toxins. Additionally, binding to ribosomes is thought to activate proteins in downstream signalling events related to immune response and apoptosis, such as mitogen-activated protein kinases. This is known as ribotoxic stress response. Trichothecenes may also induce some alterations in membrane structure, leading to increased lipid peroxidation and inhibition of electron transport activity in the mitochondria. They can further induce apoptosis through generation of reactive oxygen species. Further secondary effects of trichothecenes include inhibition of RNA and DNA synthesis, and also inhibition of mitosis. (L1948, L1949, A2962, A2963, A2964, A2980)

Signs and Symptoms · 1 item

After direct dermal application or oral ingestion, the trichothecene mycotoxins can cause rapid irritation to the skin or intestinal mucosa, including skin irritation, burning and itching, rash or blisters, and bleeding. Eye contact can cause tearing, eye pain, conjunctivitis, burning sensations about the eyes, and blurred vision for up to 1 week. Symptoms also include nausea, vomiting, fatigue, dyspnea, and acute vascular effects leading to hypotension and shock. (L1948, L1949)

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

Safety data

wgk
2
rtecs
YC9980000
ridadr
UN2811 6.1/PG 1
hs_code
38220090
risk_code
26/27/28-36/37/38-36-20/21/22-11
Signal word
Danger
Symbol(GHS)
GHS02,GHS07
hazard_code
T+,Xn,F
safety_code
22-36/37/39-45-36/37-16
Hazard statements
H225-H302+H312+H332-H319
Precautionary statements
P210-P280-P305+P351+P338
13720134139 086-15871494362 13720134139 · [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]
MedBio脉铂医药021-69568360 18916172912 · [email protected]
上海维亦特生物科技有限公司15317051735 · [email protected]
NANJING YINGWEN BIOTECHNOLOGY CO LTD+8613382787392 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
艾吉析科技(上海)有限公司17717235263 17717235263 · [email protected]
上海阿拉丁生化科技股份有限公司6206333 13167063860 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
湖北威德利化学试剂有限公司15871722230 · [email protected]
山东西亚化学有限公司4009903999 13395398332 · [email protected]
青岛贞开生物医药技术有限公司0532-58268781 18561687109 · [email protected]
上海超岚化工科技中心(原上海巢莱)0-2022843681 15618226720 · [email protected]
陕西缔都医药化工有限公司029-81154043 17391733319 · [email protected]
ATK CHEMICAL COMPANY LIMITED+undefined-21-51877795 · [email protected]
上海宏叶生物科技有限公司400-9205774 400-920-5774 · [email protected]
深圳聚合生化科技有限公司+86-400-002-6226 13028896684 · [email protected]
Aladdin Scientific[email protected]
四川恒诚致远生物科技有限公司18113192475 18113192475 · [email protected]
常州翔龙医药科技有限公司18661161657 · [email protected]
TargetMol中国(陶术生物)4008200310 15002144251 · [email protected]
北京百灵威科技有限公司18210857532 18210857532 · [email protected]
南京世洲生物科技有限公司025-85560043 13675144456 · [email protected]
上海禾午生物科技有限公司021-57886085 17317861055 · [email protected]