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Fumonisin B2 structure, CAS 116355-84-1

Fumonisin B2

CAS Number116355-84-1

Synonymsfumonisin b2solution; FUMONISIN B3; FUMONISIN B2; EINECS 201-067-0; MFCD00133350; FB2,Fumonisin B2,Ready Made; Fumonisin B2 from Fusarium moniliforme; FB2; Diquat-d4 Dibromide

Molecular FormulaC34H59NO14

Molecular Weight705.83

Purity≥96 (TLC)%

Density1.2±0.1 g/cm3

Boiling Point864.4±65.0 °C at 760 mmHg

Melting Point<3200(dec)

Flash Point

Appearancepowder

EINECS

MSDSChineseEnglish

SymbolTransport

Signal WordWarning

Cat. No.: 2A-9010649 Purity: ≥96 (TLC)%
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Quality Control of [ 116355-84-1 ] Purity: ≥96 (TLC)% SDS Specification MoL

COA NMR CNMR HPLC LC-MS
Chemical & Physical Properties
CAS Number116355-84-1
Catalog No.2A-9010649
Chinese Name伏马菌素 B2
Synonymsfumonisin b2solution; FUMONISIN B3; FUMONISIN B2; EINECS 201-067-0; MFCD00133350; FB2,Fumonisin B2,Ready Made; Fumonisin B2 from Fusarium moniliforme; FB2; Diquat-d4 Dibromide
Molecular FormulaC34H59NO14
Molecular Weight705.83
Purity≥96 (TLC)
Density1.2±0.1 g/cm3
Boiling Point864.4±65.0 °C at 760 mmHg
Melting Point<3200(dec)
Appearancepowder
Storage ConditionSeal and store at -20ºC
ApplicationFumonisin B2, a mycotoxin produced by Fusarium moniliforme found in various cereals, is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase), blocking de novo sphingolipid synthesis
HTC29221990
PubChem ID24894857
MDL NumberMFCD00133350
SMILESCCCCC(C)C(OC(=O)CC(CC(O)=O)C(O)=O)C(CC(C)CCCCCCC(O)CC(O)C(C)N)OC(=O)CC(CC(O)=O)C(O)=O
InChI1S/C34H59NO14/c1-5-6-12-21(3)32(49-31(43)18-24(34(46)47)16-29(40)41)27(48-30(42)17-23(33(44)45)15-28(38)39)14-20(2)11-9-7-8-10-13-25(36)19-26(37)22(4)35/h20-27,32,36-37H,5-19,35H2,1-4H3,(H,38,39)(H,40,41)(H,44,45)(H,46,47)
InChI KeyUXDPXZQHTDAXOZ-UHFFFAOYSA-N
NACRES CodeNA.77
UNSPSC12352202
Hazard SymbolsTransport
MSDSmsds/10649_1_116355_84_1.pdf
BioactivityFumonisin B2, a mycotoxin produced by Fusarium moniliforme in various grains, is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis[1][2]. Related Catalog Research Areas >> Infection Signaling Pathways >> Others >> Others Target Sphingosine N-acyltransferase[2] References [1]. Henry MH, et al. The toxicity of fumonisin B1, B2, and B3, individually and in combination, in chicken embryos. Poult Sci. 2001 Apr;80(4):401-7. [2]. Shephard GS, et al. Disruption of sphingolipid metabolism in non-human primates consuming diets of fumonisin-containing Fusarium moniliforme culture material. Toxicon. 1996 May;34(5):527-34. [3]. Wei T, et al. Natural occurrence of fumonisins B1 and B2 in corn in four provinces of China. Food Addit Contam Part B Surveill. 2013;6(4):270-4. Chemical & Physical Properties Density 1.2±0.1 g/cm3 Boiling Point 864.4±65.0 °C at 760 mmHg Melting Point <3200(dec) Molecular Formula C34H59NO14 Molecular Weight 705.831 Flash Point 476.6±34.3 °C Exact Mass 705.393555 PSA 268.28000 LogP 4.39 Vapour Pressure 0.0±0.6 mmHg at 25°C Index of Refraction 1.520 InChIKey UXDPXZQHTDAXOZ-FWPUDPCBSA-N SMILES CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CCCCCCC(O)CC(O)C(C)N)OC(=O)CC(CC(=O)O)C(=O)O
Use ofFumonisin B2, a mycotoxin produced by Fusarium moniliforme in various grains, is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis[1][2]. Properties Articles29 Name fumonisin B2 Synonym More Synonyms fumonisin B2 Biological Activity Description Fumonisin B2, a mycotoxin produced by Fusarium moniliforme in various grains, is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis[1][2]. Related Catalog Research Areas >> Infection Signaling Pathways >> Others >> Others Sphingosine N-acyltransferase[2] References [1]. Henry MH, et al. The toxicity of fumonisin B1, B2, and B3, individually and in combination, in chicken embryos. Poult Sci. 2001 Apr;80(4):401-7. [2]. Shephard GS, et al. Disruption of sphingolipid metabolism in non-human primates consuming diets of fumonisin-containing Fusarium moniliforme culture material. Toxicon. 1996 May;34(5):527-34. [3]. Wei T, et al. Natural occurrence of fumonisins B1 and B2 in corn in four provinces of China. Food Addit Contam Part B Surveill. 2013;6(4):270-4. Chemical & Physical Properties Molecular Formula C34H59NO14 Exact Mass 705.393555 PSA 268.28000 Index of Refraction 1.520 InChIKey UXDPXZQHTDAXOZ-FWPUDPCBSA-N SMILES CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CCCCCCC(O)CC(O)C(C)N)OC(=O)CC(CC(=O)O)C(=O)O
Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Danger Regulations: 1648 International Maritime Transport Danger Regulations: 1648 International Air Transport Danger Regulations: 1648 14.2 United Nations shipping name European land transport hazard code: ACETONITRILE, solution IMDG Code: ACETONITRILE, solution IMDG: Acetonitrile, solution 14.3 Transport hazard categories European land transport Dangerous Regulations: 3 International sea transport Dangerous Regulations: 3 International air transport Dangerous Regulations: 3 14.4 Package group European Dangerous Regulations for land transport: II International Dangerous Regulations for sea transport: II International Dangerous Regulations for air transport: II 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
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