Cornusalterin F

Details

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Internal ID 5ba570ff-1415-4c5b-9dd5-fef5625df505
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (5S,9S,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylheptan-2-yl]-5,6,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-1-one
SMILES (Canonical) CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(C(=O)C=CC4(C)C)C)C)C
SMILES (Isomeric) C[C@@H](CCCC(C)C)[C@@H]1CC[C@]2([C@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(C(=O)C=CC4(C)C)C)C)C
InChI InChI=1S/C30H48O/c1-20(2)10-9-11-21(3)22-14-18-29(7)23-12-13-25-27(4,5)17-16-26(31)30(25,8)24(23)15-19-28(22,29)6/h12,16-17,20-22,24-25H,9-11,13-15,18-19H2,1-8H3/t21-,22-,24-,25-,28-,29+,30+/m0/s1
InChI Key SRZGQWOHBSWCAT-RIZYFFEQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H48O
Molecular Weight 424.70 g/mol
Exact Mass 424.370516150 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 9.50
Atomic LogP (AlogP) 8.40
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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CHEBI:70114
Q27138453
(13alpha,14beta,17alpha,20S)-lanosta-2,7-dien-1-one

2D Structure

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2D Structure of Cornusalterin F

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 + 0.6496 64.96%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5251 52.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8953 89.53%
OATP1B3 inhibitior + 0.9332 93.32%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9305 93.05%
P-glycoprotein inhibitior + 0.6645 66.45%
P-glycoprotein substrate + 0.5438 54.38%
CYP3A4 substrate + 0.6568 65.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8664 86.64%
CYP3A4 inhibition - 0.9161 91.61%
CYP2C9 inhibition - 0.7821 78.21%
CYP2C19 inhibition - 0.6310 63.10%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.8156 81.56%
CYP2C8 inhibition - 0.6853 68.53%
CYP inhibitory promiscuity + 0.5430 54.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5104 51.04%
Eye corrosion - 0.9826 98.26%
Eye irritation - 0.9407 94.07%
Skin irritation + 0.5195 51.95%
Skin corrosion - 0.9721 97.21%
Ames mutagenesis - 0.7570 75.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7739 77.39%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6195 61.95%
skin sensitisation + 0.8101 81.01%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7370 73.70%
Acute Oral Toxicity (c) III 0.7032 70.32%
Estrogen receptor binding + 0.8603 86.03%
Androgen receptor binding + 0.7443 74.43%
Thyroid receptor binding + 0.7824 78.24%
Glucocorticoid receptor binding + 0.8709 87.09%
Aromatase binding + 0.6674 66.74%
PPAR gamma + 0.6912 69.12%
Honey bee toxicity - 0.8730 87.30%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9968 99.68%

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
CHEMBL2581 P07339 Cathepsin D 95.39% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.52% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.29% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.98% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.50% 82.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 91.05% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.52% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.25% 97.09%
CHEMBL1907 P15144 Aminopeptidase N 87.60% 93.31%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.32% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.25% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.31% 93.56%
CHEMBL2179 P04062 Beta-glucocerebrosidase 83.80% 85.31%
CHEMBL1937 Q92769 Histone deacetylase 2 82.65% 94.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.94% 96.77%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.77% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.09% 95.89%

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.
Cornus walteri

Cross-Links

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PubChem 50994305
NPASS NPC188659
LOTUS LTS0037000
wikiData Q27138453