16,25-Dihydroxy-20,24-epoxy-9,19-cyclolanostan-3-one

Details

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Internal ID 261a39f5-6e49-461e-b6c5-401493e34c5c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name (11S,12S,14S,15R,16R)-14-hydroxy-15-[(2S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one
SMILES (Canonical) CC1(C2CCC3C4(CC(C(C4(CCC35C2(C5)CCC1=O)C)C6(CCC(O6)C(C)(C)O)C)O)C)C
SMILES (Isomeric) C[C@]12CCC34CC35CCC(=O)C(C5CC[C@H]4[C@@]1(C[C@@H]([C@@H]2[C@@]6(CCC(O6)C(C)(C)O)C)O)C)(C)C
InChI InChI=1S/C30H48O4/c1-24(2)19-8-9-20-27(6)16-18(31)23(28(7)12-11-22(34-28)25(3,4)33)26(27,5)14-15-30(20)17-29(19,30)13-10-21(24)32/h18-20,22-23,31,33H,8-17H2,1-7H3/t18-,19?,20-,22?,23-,26+,27-,28-,29?,30?/m0/s1
InChI Key RBRKRLQNZMJOLD-WSZNCIIPSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O4
Molecular Weight 472.70 g/mol
Exact Mass 472.35526001 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.67
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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DTXSID40953364
(11S,12S,14S,15R,16R)-14-Hydroxy-15-[(2S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one

2D Structure

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2D Structure of 16,25-Dihydroxy-20,24-epoxy-9,19-cyclolanostan-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 - 0.5735 57.35%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7141 71.41%
OATP2B1 inhibitior - 0.7151 71.51%
OATP1B1 inhibitior + 0.8818 88.18%
OATP1B3 inhibitior + 0.9187 91.87%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7358 73.58%
BSEP inhibitior - 0.4880 48.80%
P-glycoprotein inhibitior - 0.6396 63.96%
P-glycoprotein substrate - 0.7320 73.20%
CYP3A4 substrate + 0.6686 66.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7746 77.46%
CYP3A4 inhibition - 0.5491 54.91%
CYP2C9 inhibition - 0.6991 69.91%
CYP2C19 inhibition - 0.7062 70.62%
CYP2D6 inhibition - 0.9521 95.21%
CYP1A2 inhibition - 0.6725 67.25%
CYP2C8 inhibition - 0.6255 62.55%
CYP inhibitory promiscuity - 0.9177 91.77%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5795 57.95%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9388 93.88%
Skin irritation - 0.5662 56.62%
Skin corrosion - 0.9070 90.70%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4377 43.77%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6716 67.16%
skin sensitisation - 0.8307 83.07%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.8150 81.50%
Acute Oral Toxicity (c) I 0.3365 33.65%
Estrogen receptor binding + 0.7330 73.30%
Androgen receptor binding + 0.7199 71.99%
Thyroid receptor binding + 0.6886 68.86%
Glucocorticoid receptor binding + 0.7137 71.37%
Aromatase binding + 0.7991 79.91%
PPAR gamma + 0.5703 57.03%
Honey bee toxicity - 0.8265 82.65%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9626 96.26%

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 97.14% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.59% 97.25%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.28% 83.57%
CHEMBL204 P00734 Thrombin 91.05% 96.01%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.96% 95.56%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.89% 96.61%
CHEMBL230 P35354 Cyclooxygenase-2 88.70% 89.63%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.85% 85.30%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.76% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.40% 100.00%
CHEMBL2581 P07339 Cathepsin D 87.32% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.77% 97.09%
CHEMBL259 P32245 Melanocortin receptor 4 84.72% 95.38%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.66% 89.34%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.66% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.44% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 81.96% 94.75%
CHEMBL1902 P62942 FK506-binding protein 1A 81.44% 97.05%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.13% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.72% 92.62%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.49% 82.69%
CHEMBL284 P27487 Dipeptidyl peptidase IV 80.25% 95.69%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.18% 96.95%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 80.01% 98.00%

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.
Parthenium argentatum
Parthenium lozanianum

Cross-Links

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PubChem 193674
LOTUS LTS0199300
wikiData Q82932203