Fusaristerol C

Details

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Internal ID 81a771a1-fdf2-40ce-a90b-2be6b400e266
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,6R,9R,10S,13S,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13,17-trimethyl-2,3,4,5,6,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,6,9-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H48O3/c1-18(2)19(3)8-9-20(4)26(5)13-11-22-23-17-25(31)24-16-21(30)10-12-28(24,7)29(23,32)15-14-27(22,26)6/h8-9,17-22,24-25,30-32H,10-16H2,1-7H3/b9-8+/t19-,20+,21-,22-,24?,25+,26+,27-,28-,29-/m0/s1
InChI Key IJXNPQGUSGUOQC-JCLZURILSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H48O3
Molecular Weight 444.70 g/mol
Exact Mass 444.36034539 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.89
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Fusaristerol C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5434 54.34%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6838 68.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7936 79.36%
OATP1B3 inhibitior + 0.9670 96.70%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.7705 77.05%
P-glycoprotein inhibitior - 0.6400 64.00%
P-glycoprotein substrate - 0.5739 57.39%
CYP3A4 substrate + 0.6516 65.16%
CYP2C9 substrate - 0.7657 76.57%
CYP2D6 substrate - 0.7563 75.63%
CYP3A4 inhibition - 0.8741 87.41%
CYP2C9 inhibition - 0.9130 91.30%
CYP2C19 inhibition - 0.8936 89.36%
CYP2D6 inhibition - 0.9460 94.60%
CYP1A2 inhibition - 0.9024 90.24%
CYP2C8 inhibition - 0.5681 56.81%
CYP inhibitory promiscuity - 0.7172 71.72%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5463 54.63%
Eye corrosion - 0.9938 99.38%
Eye irritation - 0.9535 95.35%
Skin irritation + 0.6084 60.84%
Skin corrosion - 0.9575 95.75%
Ames mutagenesis - 0.6470 64.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5171 51.71%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5985 59.85%
skin sensitisation + 0.4728 47.28%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 1.0000 100.00%
Nephrotoxicity - 0.7384 73.84%
Acute Oral Toxicity (c) III 0.6265 62.65%
Estrogen receptor binding + 0.7835 78.35%
Androgen receptor binding + 0.7011 70.11%
Thyroid receptor binding + 0.6618 66.18%
Glucocorticoid receptor binding + 0.6916 69.16%
Aromatase binding - 0.4887 48.87%
PPAR gamma - 0.5112 51.12%
Honey bee toxicity - 0.7596 75.96%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9905 99.05%

Targets

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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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.62% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 95.81% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.11% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 90.55% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.45% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.22% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.52% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 88.56% 90.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.22% 97.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.15% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.06% 91.07%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.97% 94.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.78% 100.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 82.96% 91.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.66% 97.25%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 81.47% 97.23%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.45% 94.62%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.00% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 146682466
LOTUS LTS0219466
wikiData Q105114206