Fumonisin B2 is known as a fumonisin mycotoxin.
| Internal ID | a170e8a8-5e58-4593-9ecf-496872045f17 |
| Taxonomy | Organic acids and derivatives > Carboxylic acids and derivatives > Fumonisins |
| IUPAC Name | 2-[2-[19-amino-6-(3,4-dicarboxybutanoyloxy)-16,18-dihydroxy-5,9-dimethylicosan-7-yl]oxy-2-oxoethyl]butanedioic acid |
| SMILES (Canonical) | |
| SMILES (Isomeric) | |
| InChI | InChI=1S/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 Key | UXDPXZQHTDAXOZ-UHFFFAOYSA-N |
| Popularity | 2 references in papers |
| Molecular Formula | C34H59NO14 |
| Molecular Weight | 705.80 g/mol |
| Exact Mass | 705.39355556 g/mol |
| Topological Polar Surface Area (TPSA) | 268.00 Ų |
| XlogP | 1.20 |
| Atomic LogP (AlogP) | 3.59 |
| H-Bond Acceptor | 11 |
| H-Bond Donor | 7 |
| Rotatable Bonds | 29 |
| UXDPXZQHTDAXOZ-UHFFFAOYSA-N |
| AKOS030255413 |
| AS-78700 |
| NS00000146 |
| Fumonisin B2 is known as a fumonisin mycotoxin. |
| Fumonisin B2 from Fusarium moniliforme, sphingosine N-acyltransferase inhibitor |
| 1,1'-[(1S,2R)-1-[(2S,9R,11S,12S)-12-Amino-9,11-dihydroxy-2-methyltridecyl]-2-[(1R)-1-methylpentyl]-1,2-ethanediyl]ester-1,2,3-propanetricarboxylic acid |
| 2-[2-[13-amino-1-[1-(3,4-dicarboxybutanoyloxy)-2-methyl-hexyl]-10,12-dihydroxy-3-methyl-tetradecoxy]-2-oxo-ethyl]butanedioic acid |
| Target | Value | Probability (raw) | Probability (%) |
|---|---|---|---|
| Human Intestinal Absorption | + | 0.6536 | 65.36% |
| Caco-2 | - | 0.8472 | 84.72% |
| Blood Brain Barrier | - | 0.5250 | 52.50% |
| Human oral bioavailability | - | 0.6143 | 61.43% |
| Subcellular localzation | Mitochondria | 0.5542 | 55.42% |
| OATP2B1 inhibitior | - | 0.5658 | 56.58% |
| OATP1B1 inhibitior | + | 0.8827 | 88.27% |
| OATP1B3 inhibitior | + | 0.9267 | 92.67% |
| MATE1 inhibitior | - | 1.0000 | 100.00% |
| OCT2 inhibitior | - | 0.9250 | 92.50% |
| BSEP inhibitior | + | 0.6748 | 67.48% |
| P-glycoprotein inhibitior | + | 0.7143 | 71.43% |
| P-glycoprotein substrate | - | 0.7977 | 79.77% |
| CYP3A4 substrate | + | 0.6071 | 60.71% |
| CYP2C9 substrate | - | 0.5982 | 59.82% |
| CYP2D6 substrate | - | 0.7891 | 78.91% |
| CYP3A4 inhibition | - | 0.6368 | 63.68% |
| CYP2C9 inhibition | - | 0.8342 | 83.42% |
| CYP2C19 inhibition | - | 0.7989 | 79.89% |
| CYP2D6 inhibition | - | 0.8325 | 83.25% |
| CYP1A2 inhibition | - | 0.5945 | 59.45% |
| CYP2C8 inhibition | - | 0.6442 | 64.42% |
| CYP inhibitory promiscuity | - | 0.9392 | 93.92% |
| UGT catelyzed | + | 0.8000 | 80.00% |
| Carcinogenicity (binary) | - | 0.8600 | 86.00% |
| Carcinogenicity (trinary) | Non-required | 0.6442 | 64.42% |
| Eye corrosion | - | 0.9784 | 97.84% |
| Eye irritation | - | 0.9013 | 90.13% |
| Skin irritation | - | 0.8659 | 86.59% |
| Skin corrosion | - | 0.9528 | 95.28% |
| Ames mutagenesis | - | 1.0000 | 100.00% |
| Human Ether-a-go-go-Related Gene inhibition | - | 0.3981 | 39.81% |
| Micronuclear | - | 0.5900 | 59.00% |
| Hepatotoxicity | - | 0.5448 | 54.48% |
| skin sensitisation | - | 0.8963 | 89.63% |
| Respiratory toxicity | - | 0.5222 | 52.22% |
| Reproductive toxicity | - | 0.7566 | 75.66% |
| Mitochondrial toxicity | - | 0.6000 | 60.00% |
| Nephrotoxicity | + | 0.5763 | 57.63% |
| Acute Oral Toxicity (c) | III | 0.6849 | 68.49% |
| Estrogen receptor binding | + | 0.7875 | 78.75% |
| Androgen receptor binding | + | 0.6980 | 69.80% |
| Thyroid receptor binding | - | 0.5416 | 54.16% |
| Glucocorticoid receptor binding | + | 0.6850 | 68.50% |
| Aromatase binding | + | 0.5857 | 58.57% |
| PPAR gamma | + | 0.5509 | 55.09% |
| Honey bee toxicity | - | 0.8916 | 89.16% |
| Biodegradation | - | 0.7500 | 75.00% |
| Crustacea aquatic toxicity | - | 0.5200 | 52.00% |
| Fish aquatic toxicity | + | 0.7697 | 76.97% |
Proven Targets:
| CHEMBL ID | UniProt ID | Name | Min activity | Assay type | Source |
|---|---|---|---|---|---|
| No proven targets yet! | |||||
Predicted Targets (via Super-PRED):
| CHEMBL ID | UniProt ID | Name | Probability | Model accuracy |
|---|---|---|---|---|
| CHEMBL2581 | P07339 | Cathepsin D | 98.51% | 98.95% |
| CHEMBL221 | P23219 | Cyclooxygenase-1 | 98.30% | 90.17% |
| CHEMBL3251 | P19838 | Nuclear factor NF-kappa-B p105 subunit | 98.16% | 96.09% |
| CHEMBL236 | P41143 | Delta opioid receptor | 97.94% | 99.35% |
| CHEMBL4040 | P28482 | MAP kinase ERK2 | 96.44% | 83.82% |
| CHEMBL1907 | P15144 | Aminopeptidase N | 95.54% | 93.31% |
| CHEMBL3892 | Q99500 | Sphingosine 1-phosphate receptor Edg-3 | 95.15% | 97.29% |
| CHEMBL3359 | P21462 | Formyl peptide receptor 1 | 94.56% | 93.56% |
| CHEMBL5619 | P27695 | DNA-(apurinic or apyrimidinic site) lyase | 93.92% | 91.11% |
| CHEMBL3060 | Q9Y345 | Glycine transporter 2 | 93.46% | 99.17% |
| CHEMBL4793 | Q86TI2 | Dipeptidyl peptidase IX | 91.11% | 96.95% |
| CHEMBL4657 | Q6V1X1 | Dipeptidyl peptidase VIII | 91.05% | 97.21% |
| CHEMBL3130 | O00329 | PI3-kinase p110-delta subunit | 88.34% | 96.47% |
| CHEMBL2274 | Q9H228 | Sphingosine 1-phosphate receptor Edg-8 | 88.01% | 100.00% |
| CHEMBL1821 | P08173 | Muscarinic acetylcholine receptor M4 | 87.92% | 94.08% |
| CHEMBL4227 | P25090 | Lipoxin A4 receptor | 87.48% | 100.00% |
| CHEMBL5845 | P23415 | Glycine receptor subunit alpha-1 | 87.31% | 90.71% |
| CHEMBL2955 | O95136 | Sphingosine 1-phosphate receptor Edg-5 | 87.20% | 92.86% |
| CHEMBL1907591 | P30926 | Neuronal acetylcholine receptor; alpha4/beta4 | 85.08% | 100.00% |
| CHEMBL3776 | Q14790 | Caspase-8 | 83.42% | 97.06% |
| CHEMBL2001 | Q9H244 | Purinergic receptor P2Y12 | 82.92% | 96.00% |
| CHEMBL2514 | O95665 | Neurotensin receptor 2 | 82.55% | 100.00% |
| CHEMBL3091268 | Q92753 | Nuclear receptor ROR-beta | 82.15% | 95.50% |
| CHEMBL1255126 | O15151 | Protein Mdm4 | 81.01% | 90.20% |
Below are displayed all the plants proven (via scientific papers) to contain this
compound!
To see more specific details click the taxa you are interested in.
To see more specific details click the taxa you are interested in.
| There are no matching plants. |
| PubChem | 3432 |
| LOTUS | LTS0169790 |
| wikiData | Q104199027 |