Fucostenone

Details

Top
Internal ID 357e46a2-31fc-4d3f-be9b-32b5a19c5458
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Stigmastanes and derivatives
IUPAC Name (8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(E,2R)-5-propan-2-ylhept-5-en-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
SMILES (Canonical) CC=C(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C
SMILES (Isomeric) C/C=C(\CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)C)/C(C)C
InChI InChI=1S/C29H46O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h7,18-20,24-27H,8-17H2,1-6H3/b21-7+/t20-,24+,25-,26+,27+,28+,29-/m1/s1
InChI Key JKNOXDGSYQSJQT-IOYZGJOASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C29H46O
Molecular Weight 410.70 g/mol
Exact Mass 410.354866087 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 8.80
Atomic LogP (AlogP) 8.15
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
Stigmasta-4,24(28)-dien-3-one, (24E)-
53755-09-2
CHEMBL517299

2D Structure

Top
2D Structure of Fucostenone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5869 58.69%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5591 55.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8320 83.20%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9744 97.44%
P-glycoprotein inhibitior + 0.8334 83.34%
P-glycoprotein substrate - 0.7386 73.86%
CYP3A4 substrate + 0.7448 74.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8713 87.13%
CYP3A4 inhibition - 0.8867 88.67%
CYP2C9 inhibition - 0.8897 88.97%
CYP2C19 inhibition - 0.7062 70.62%
CYP2D6 inhibition - 0.9594 95.94%
CYP1A2 inhibition - 0.8927 89.27%
CYP2C8 inhibition - 0.8651 86.51%
CYP inhibitory promiscuity - 0.6104 61.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5158 51.58%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.9696 96.96%
Skin irritation + 0.6133 61.33%
Skin corrosion - 0.9711 97.11%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4285 42.85%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5169 51.69%
skin sensitisation + 0.8120 81.20%
Respiratory toxicity + 0.9889 98.89%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.9140 91.40%
Acute Oral Toxicity (c) III 0.7698 76.98%
Estrogen receptor binding + 0.9168 91.68%
Androgen receptor binding + 0.8301 83.01%
Thyroid receptor binding + 0.7637 76.37%
Glucocorticoid receptor binding + 0.8948 89.48%
Aromatase binding + 0.6398 63.98%
PPAR gamma + 0.6350 63.50%
Honey bee toxicity - 0.7216 72.16%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9926 99.26%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.13% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.82% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.20% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 96.66% 100.00%
CHEMBL240 Q12809 HERG 94.60% 89.76%
CHEMBL1871 P10275 Androgen Receptor 94.39% 96.43%
CHEMBL2581 P07339 Cathepsin D 94.26% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.80% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 92.73% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.50% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.71% 93.99%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.98% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.88% 90.71%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 88.69% 85.30%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 88.09% 94.78%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.90% 82.69%
CHEMBL226 P30542 Adenosine A1 receptor 85.72% 95.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.23% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.90% 92.62%
CHEMBL4581 P52732 Kinesin-like protein 1 82.43% 93.18%
CHEMBL221 P23219 Cyclooxygenase-1 81.95% 90.17%

Plants that contains it

Top
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.
Melia azedarach

Cross-Links

Top
PubChem 11795872
NPASS NPC282593
LOTUS LTS0085364
wikiData Q105130354