trans-Feruloyl campestanol

Details

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Internal ID 46e6924f-645f-4739-a889-433b2f21261a
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (E,6R,9R)-9-[(3S,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-1-(4-hydroxy-3-methoxyphenyl)-5,6-dimethyldec-1-en-3-one
SMILES (Canonical) CC(CCC(C)C(C)CC(=O)C=CC1=CC(=C(C=C1)O)OC)C2CCC3C2(CCC4C3CCC5C4(CCC(C5)O)C)C
SMILES (Isomeric) C[C@H](CC[C@@H](C)C(C)CC(=O)/C=C/C1=CC(=C(C=C1)O)OC)[C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC[C@@H]5[C@@]4(CC[C@@H](C5)O)C)C
InChI InChI=1S/C38H58O4/c1-24(26(3)21-29(39)12-9-27-10-16-35(41)36(22-27)42-6)7-8-25(2)32-14-15-33-31-13-11-28-23-30(40)17-19-37(28,4)34(31)18-20-38(32,33)5/h9-10,12,16,22,24-26,28,30-34,40-41H,7-8,11,13-15,17-21,23H2,1-6H3/b12-9+/t24-,25-,26?,28+,30+,31+,32-,33+,34+,37+,38-/m1/s1
InChI Key JAZJNMDSVDHBFN-AVKUBCOBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C38H58O4
Molecular Weight 578.90 g/mol
Exact Mass 578.43351033 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 10.40
Atomic LogP (AlogP) 9.08
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of trans-Feruloyl campestanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 - 0.7994 79.94%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8215 82.15%
OATP2B1 inhibitior - 0.5617 56.17%
OATP1B1 inhibitior + 0.7572 75.72%
OATP1B3 inhibitior - 0.2162 21.62%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9835 98.35%
P-glycoprotein inhibitior + 0.7105 71.05%
P-glycoprotein substrate + 0.5913 59.13%
CYP3A4 substrate + 0.7468 74.68%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.8070 80.70%
CYP3A4 inhibition - 0.6436 64.36%
CYP2C9 inhibition - 0.7905 79.05%
CYP2C19 inhibition - 0.7544 75.44%
CYP2D6 inhibition - 0.9286 92.86%
CYP1A2 inhibition + 0.7303 73.03%
CYP2C8 inhibition + 0.6644 66.44%
CYP inhibitory promiscuity - 0.7523 75.23%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6469 64.69%
Eye corrosion - 0.9951 99.51%
Eye irritation - 0.9382 93.82%
Skin irritation - 0.5169 51.69%
Skin corrosion - 0.9536 95.36%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7065 70.65%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6656 66.56%
skin sensitisation - 0.8960 89.60%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.9449 94.49%
Acute Oral Toxicity (c) III 0.4099 40.99%
Estrogen receptor binding + 0.7646 76.46%
Androgen receptor binding + 0.8651 86.51%
Thyroid receptor binding - 0.5301 53.01%
Glucocorticoid receptor binding + 0.6522 65.22%
Aromatase binding + 0.6600 66.00%
PPAR gamma + 0.6677 66.77%
Honey bee toxicity - 0.6664 66.64%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5045 50.45%
Fish aquatic toxicity + 0.9945 99.45%

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 99.46% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.62% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.52% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.37% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.03% 94.45%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 94.52% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.81% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 93.02% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.48% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.56% 97.09%
CHEMBL2179 P04062 Beta-glucocerebrosidase 90.77% 85.31%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.89% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.47% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 87.23% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.09% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.58% 95.89%
CHEMBL4208 P20618 Proteasome component C5 84.28% 90.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.81% 100.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 82.83% 89.50%
CHEMBL340 P08684 Cytochrome P450 3A4 82.46% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.44% 92.62%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.21% 91.07%
CHEMBL2535 P11166 Glucose transporter 81.09% 98.75%
CHEMBL4581 P52732 Kinesin-like protein 1 80.81% 93.18%

Plants that contains it

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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.
Coix lacryma-jobi

Cross-Links

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PubChem 129847772
LOTUS LTS0159291
wikiData Q105124167