xerophilusin XI

Details

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Internal ID ad9c5c80-28d2-4d77-bcda-2a6d3abe74b5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name (1R,2S,3S,5S,8R,9R,10S,11R,16S,18R)-3,9,10,18-tetrahydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one
SMILES (Canonical) CC1(CCCC23C1C(C(C45C2C(CC(C4O)C(=C)C5=O)O)(OC3OC)O)O)C
SMILES (Isomeric) CC1(CCC[C@]23[C@@H]1[C@@H]([C@@]([C@]45[C@H]2[C@H](C[C@H]([C@H]4O)C(=C)C5=O)O)(O[C@@H]3OC)O)O)C
InChI InChI=1S/C21H30O7/c1-9-10-8-11(22)12-19-7-5-6-18(2,3)13(19)16(25)21(26,28-17(19)27-4)20(12,14(9)23)15(10)24/h10-13,15-17,22,24-26H,1,5-8H2,2-4H3/t10-,11-,12-,13+,15+,16-,17-,19+,20-,21-/m0/s1
InChI Key XHYABSFBWXRDOI-QUTINQDXSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H30O7
Molecular Weight 394.50 g/mol
Exact Mass 394.19915329 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.35
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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CHEMBL399079

2D Structure

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2D Structure of xerophilusin XI

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9043 90.43%
Caco-2 - 0.7009 70.09%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5999 59.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8029 80.29%
OATP1B3 inhibitior + 0.8600 86.00%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7571 75.71%
BSEP inhibitior - 0.9027 90.27%
P-glycoprotein inhibitior - 0.8102 81.02%
P-glycoprotein substrate - 0.6719 67.19%
CYP3A4 substrate + 0.6669 66.69%
CYP2C9 substrate - 0.8135 81.35%
CYP2D6 substrate - 0.8356 83.56%
CYP3A4 inhibition - 0.7188 71.88%
CYP2C9 inhibition - 0.6983 69.83%
CYP2C19 inhibition - 0.6940 69.40%
CYP2D6 inhibition - 0.9166 91.66%
CYP1A2 inhibition - 0.7479 74.79%
CYP2C8 inhibition - 0.6084 60.84%
CYP inhibitory promiscuity - 0.9384 93.84%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6727 67.27%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9389 93.89%
Skin irritation - 0.5532 55.32%
Skin corrosion - 0.9150 91.50%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6128 61.28%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5411 54.11%
skin sensitisation - 0.7956 79.56%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.5725 57.25%
Acute Oral Toxicity (c) III 0.3289 32.89%
Estrogen receptor binding + 0.7442 74.42%
Androgen receptor binding + 0.7125 71.25%
Thyroid receptor binding + 0.6498 64.98%
Glucocorticoid receptor binding + 0.6775 67.75%
Aromatase binding + 0.7051 70.51%
PPAR gamma + 0.6231 62.31%
Honey bee toxicity - 0.6813 68.13%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9602 96.02%

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 97.68% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.85% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.79% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.27% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.56% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.14% 98.95%
CHEMBL1902 P62942 FK506-binding protein 1A 84.73% 97.05%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.58% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.61% 86.33%
CHEMBL1871 P10275 Androgen Receptor 83.40% 96.43%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.30% 91.07%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.05% 95.50%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 82.04% 91.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.53% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.52% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.25% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 81.06% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.72% 94.00%
CHEMBL2996 Q05655 Protein kinase C delta 80.70% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.45% 95.56%

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.
Isodon xerophilus

Cross-Links

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PubChem 44445749
LOTUS LTS0145444
wikiData Q105328368