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FUMONISIN B1

CAS No.
116355-83-0
Chemical Name:
FUMONISIN B1
Synonyms
FB1;MACROFUSINE;FUMONISIN B1;B1 Fumonisin B1;Fumonisin B1,96%;FUMONISIN B1 98%;Fumonisin B1 ,95%;Fumonisin B1 (FB1);fumonisin b1solution;FuMonisin B1, 96% 1MG
CBNumber:
CB1773259
Molecular Formula:
C34H59NO15
Molecular Weight:
721.83
MDL Number:
MFCD00133349
MOL File:
116355-83-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-21 10:31:43
Product description Number Pack Size Price
Fumonisin B₁, Fusarium moniliforme - CAS 116355-83-0 - Calbiochem A cell-permeable mycotoxin that inhibits sphingolipid biosynthesis in rat kidney and in liver microsomes by inhibition of sphingosine N-acyltransferase (ceramide synthase; IC?? = 100 nM). 344850-M 1mg $109
Fumonisin B1 solution 50?μg/mL in acetonitrile: water, analytical standard 34139 1ML $323
Fumonisin B1 reference material 32936 5mg $1400
Fumonisin B1 ≥95% 62580 1mg $86
Fumonisin B1 ≥95% 62580 5mg $409
More product size

FUMONISIN B1 Properties

Melting point >60oC
Boiling point 713.81°C (rough estimate)
Density 1.2207 (rough estimate)
refractive index 1.6630 (estimate)
Flash point 6 °C
storage temp. 2-8°C
solubility Soluble in Water (up to 25 mg/ml).
form Powder
pka 3+-.0.23(Predicted)
color White to tan
biological source Fusarium sp. (Fusarium moniliforme)
Stability Stable for 2 years from date of purchase as supplied. Solutions in distilled water may be stored at -20° for up to 3 months.
InChIKey GPIYLYZFGAXYSU-UHFFFAOYSA-N
SMILES C(CC(C)CC(O)CCCCC(O)CC(O)C(N)C)(OC(=O)CC(C(=O)O)CC(=O)O)C(CC(C)CCC)OC(=O)CC(C(=O)O)CC(=O)O
Toxicology and Carcinogenesis Toxicology and Carcinogenesis Studies of Fumonisin B1 (CASRN 116355-83-0) in F344/N Rats and B6C3F1 Mice (Feed Studies)
CAS DataBase Reference 116355-83-0
FDA UNII 3ZZM97XZ32
Proposition 65 List Fumonisin B1
IARC 2B (Vol. 56) 1993, 2B (Vol. 82) 2002
UNSPSC Code 85151701
NACRES NA.32

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS08
Signal word  Danger
Hazard statements  H301-H351-H361d-H373
Precautionary statements  P201-P301+P310+P330
target organs Kidney,Liver
PPE Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  Xn,T,F
Risk Statements  40-36-20/21/22-11
Safety Statements  36/37-16-26-45
RIDADR  3172
WGK Germany  3
RTECS  TZ8350000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29221990
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral
Carc. 2
Repr. 2
STOT RE 2
Hazardous Substances Data 116355-83-0(Hazardous Substances Data)

FUMONISIN B1 price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 344850-M Fumonisin B₁, Fusarium moniliforme - CAS 116355-83-0 - Calbiochem A cell-permeable mycotoxin that inhibits sphingolipid biosynthesis in rat kidney and in liver microsomes by inhibition of sphingosine N-acyltransferase (ceramide synthase; IC?? = 100 nM). 116355-83-0 1mg $109 2026-04-30 Buy
Sigma-Aldrich 34139 Fumonisin B1 solution 50?μg/mL in acetonitrile: water, analytical standard 116355-83-0 1ML $323 2026-04-30 Buy
Sigma-Aldrich 32936 Fumonisin B1 reference material 116355-83-0 5mg $1400 2026-04-30 Buy
Cayman Chemical 62580 Fumonisin B1 ≥95% 116355-83-0 1mg $86 2026-04-30 Buy
Cayman Chemical 62580 Fumonisin B1 ≥95% 116355-83-0 5mg $409 2026-04-30 Buy
Product number Packaging Price Buy
344850-M 1mg $109 Buy
34139 1ML $323 Buy
32936 5mg $1400 Buy
62580 1mg $86 Buy
62580 5mg $409 Buy

FUMONISIN B1 Chemical Properties,Uses,Production

Description

Fumonisin B1 (116355-83-0) inhibits ceramide synthesis (sphinganine N-acyltransferase), IC50 = 100 nM. Inhibits de novo sphingolipid biosynthesis (IC50 = 0.7 μM) thereby blocking glycosphingolipid production.

Chemical Properties

white to tan powder

Uses

A serine/threonine phosphatase inhibitor.

Uses

A mycotoxin produced by mold associated with corn. Fungal metabolite believed to cause leukoencephalomalacia in horses.

Uses

Fumonisin B1 is a major analogue of a family of potent mycotoxins produced by various Fusarium species, associated with animal toxicity worldwide. In vitro, fumonisin B1 inhibits sphingosine N-acyl-transferase (ceramide synthase) and blocks the growth of axons.

Definition

ChEBI: Fumonisin B1 is a diester that results from the condensation of the 1-carboxy groups of two molecules of propane-1,2,3-tricarboxylic acid with hydroxy groups at positions 14 and 15 of (2S,3S,5R,10R,12S,14S,15R,16R)-2-amino-12,16-dimethylicosane-3,5,10,14,15-pentol. It has a role as a metabolite and a carcinogenic agent. It is a fumonisin, a primary amino compound, a diester and a triol. It is functionally related to a (2S,3S,5R,10R,12S,14S,15R,16R)-2-amino-12,16-dimethylicosane-3,5,10,14,15-pentol. It is a conjugate acid of a fumonisin B1(3-).

General Description

Fumonisin B1 is a neurotoxin and a phytotoxin. A cell-permeable mycotoxin that inhibits sphingolipid biosynthesis in rat kidney and in liver microsomes by inhibition of sphingosine N-acyltransferase (ceramide synthase) (IC50 = 100 nM). Cellular effects also appear to be induced by micromolar levels of FB1. Because it inhibits ceramide synthase activity, it elevates cellular levels of sphingoid bases, including sphinganine, resulting in overall inhibition of sphingolipid biosynthesis. Preferentially inhibits sphingomyelin biosynthesis in neuronal cells. Has carcinogenic properties.

Biological Activity

Mycotoxin produced by Fusarium moniliforme . Potently inhibits sphingosine N-acyltransferase (ceramide synthase), causing an accumulation of sphingoid bases (IC 50 ~ 75 nM). Also inhibits protein phosphatases; IC 50 values are 80, 300, 400, 500 and 3000 μ M for PP5, PP2C α , PP2A, PP1 γ 2 and PP2B respectively.

Biochem/physiol Actions

Fumonisin B1 acts as a hepatocarcinogen and causes hepatotoxicity in rats. In horses, it causes leukoencephalitis, and in pigs, it causes pulmonary edema syndrome. In China and southern parts of Africa, it is linked with high incidence of esophageal cancer in humans. It acts as an inhibitor of sphingosine N-acyltransferase enzyme (ceramide synthase), related to structural similarities between fumonisin B1 and sphingoid bases like sphingosine.

storage

Store at +4°C

References

[1] A H MERRILL. Fumonisin B1 inhibits sphingosine (sphinganine) N-acyltransferase and de novo sphingolipid biosynthesis in cultured neurons in situ.[J]. The Journal of Biological Chemistry, 1993, 268 36: 27299-27306.

FUMONISIN B1 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 211)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
BOC Sciences
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TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32467 58
Hubei Ipure Biology Co., Ltd
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HONG KONG IPURE BIOLOGY CO.,LIMITED
86 18062405514 18062405514 ada@ipurechemical.com CHINA 3461 58
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+86-571-87711850 market18@leapchem.com China 43333 58
Aladdin Scientific
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DAYANG CHEM (HANGZHOU) CO.,LTD
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NANJING YINGWEN BIOTECHNOLOGY CO LTD
+8613382787392 sales@aeechem.com China 10000 58
QUALITY CONTROL SOLUTIONS LTD.
+86-0755-66853366 +86-13670046396 export03@qcsrm.com China 24342 58

View Lastest Price from FUMONISIN B1 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fumonisin B1 pictures 2026-04-20 Fumonisin B1
116355-83-0
US $292.00 / mg 10g TargetMol Chemicals Inc.
  • Fumonisin B1 pictures
  • Fumonisin B1
    116355-83-0
  • US $292.00 / mg
  • TargetMol Chemicals Inc.
MACROFUSINE FUMONISIN B1 FUMONISIN B1, FUSARIUM MONILIFORME FB1 1,2,3-PROPANETRICARBOXYLIC ACID 1,1'-[1-(12-AMINO-4,9,11-TRIHYDROXY-2-METHYLTRIDECYL)-2-(1-METHYLPENTYL)-1,2-ETHANEDIYL] ESTER 1,2,3-PROPANETRICARBOXYLIC ACID 1,1'-[12-AMINO-4,9,11-TRIHYDROXY-2-METHYLTRIDECYL)-2-(1-METHYLPENTYL)-1,2-ETHANEDIYL]ESTER 1,2,3-propanetricarboxylicacid,1,1’-(1-(12-amino-4,9,11-trihydroxy-2-methyltr idecyl)-2-(1-methylpentyl)-1,2-ethanediyl)ester FUMONISIN B1 (MACROFUSINE) \ SPHINGOSINE FUMONISIN B1 FROM FUSARIUM MONILIFORME 1,2,3-Propanetricarboxylic acid, 1,1[1-(12-amino-4,9,11-trihydroxy-2-methyl-tridecyl)-2-(1-methylpentyl)-1,2-ethane-diyl]ester, Macrofusine FumonisinB1 from Fusarium moniliforme, Macrofusine Fumonisin B1,96% 1,1'-[(1S,2R)-1-[(2S,4R,9R,11S,12S)-12-Amino-4,9,11-trihydroxy-2-methyltridecyl]-2-[(1R)-1-methylpentyl]-1,2-ethanediyl-1,2,3-(2R,2'R)-propanetricarboxylicacidester. Fumonisin B1 ,95% FuMonisin B1, 96% 1MG (2R,2'R)-1,2,3-Propanetricarboxylic Acid 1,1'-[(1S,2R)-1-[(2S,4R,9R,11S,12S)-12-AMino-4,9,11-trihydroxy-2-Methyltridecyl]-2-[(1R)-1-Methylpentyl]-1,2-ethanediyl] Ester FUMONISIN B1 98% 1,2,3-Propanetricarboxylic acid, 1,1-(1S,2R)-1-(2S,4R,9R,11S,12S)-12-amino-4,9,11-trihydroxy-2-methyltridecyl-2-(1R)-1-methylpentyl-1,2-ethanediyl ester, (2R,2R)- fumonisin b1solution Fumonisin B1 (2R,2'R)-1,2,3-Propanetricarboxylic acid 1,1'-[(1S,2R)-1-[(2S,4R,9R,11S,12S)-12-amino-4,9,11-trihydroxy-2-methyltridecyl]-2-[(1R)-1-methylpentyl]-1,2-ethanediyl] ester Standard Solution Fumonisin B1 Fumonisin B1 (FB1) Fumonisin B, Fusarium moniliforme - CAS 116355-83-0 - Calbiochem Fumonisin B1 Ready Made Solution Fumonisin B1, 96%, from Fusarium moniliforme Fumonisin B1 Solution [ 50μg/ml Acetonitrile:Water(1:1) Solution] Fumonisin B1 50ug /ml in ACN:H2O 1:1 B1 Fumonisin B1 (2R)-2-(2-{[(5R,6R,7S,9S,11R,16R,18S,19S)-19-amino-6-{[(3R)-3,4-dicarboxybutanoyl]oxy}-11,16,18-trihydroxy-5,9-dimethylicosan-7-yl]oxy}-2-oxoethyl)butanedioic acid Fumonisin B1 50 μg/ml Acetonitrile/Water Fumonisine B1 in Acetonitrile:Water=1:1 Fumonisine B1 in Acetonitrile FumonisinB1 standard substance Fumonisin B1 from Fusarium moniliforme Fumonisin B1 Fumonisin B1, Fusarium moniliforme Fumonisin B1 solution Fumonisin B?, Fusarium moniliforme - CAS 116355-83-0 - Calbiochem[344850-1MG] Fumonisin B?, Fusarium moniliforme - CAS 116355-83-0 - Calbiochem[344850] 116355-83-0 C34H59NO15 Biochemicals and Reagents BioChemical Enzyme Inhibitors by Enzyme Enzymes, Inhibitors, and Substrates Enzyme Inhibitors R to Z Sphingosine N-acyltransferase antibiotic Miscellaneous Natural Products Amines Chiral Reagents Intermediates & Fine Chemicals Pharmaceuticals