Pterisolic acid D

Details

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Internal ID 74492614-efda-4e3c-8ca6-593830a05415
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name (1S,3R,4S,5R,9R,10R,13R,14R)-3,10-dihydroxy-5,9,14-trimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid
SMILES (Canonical) CC1C2CCC3(C4(CCCC(C4C(CC3(C2)C1=O)O)(C)C(=O)O)C)O
SMILES (Isomeric) C[C@@H]1[C@@H]2CC[C@]3([C@@]4(CCC[C@@]([C@H]4[C@@H](C[C@]3(C2)C1=O)O)(C)C(=O)O)C)O
InChI InChI=1S/C20H30O5/c1-11-12-5-8-20(25)18(3)7-4-6-17(2,16(23)24)14(18)13(21)10-19(20,9-12)15(11)22/h11-14,21,25H,4-10H2,1-3H3,(H,23,24)/t11-,12-,13-,14-,17-,18-,19-,20-/m1/s1
InChI Key JSIHLPUZVXXTHU-VDRBZVAGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O5
Molecular Weight 350.40 g/mol
Exact Mass 350.20932405 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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1401419-88-2
Kauran-18-oic acid, 6,9-dihydroxy-15-oxo-, (4alpha,6beta)-
(1S,3R,4S,5R,9R,10R,13R,14R)-3,10-dihydroxy-5,9,14-trimethyl-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid
DTXSID101222406
AKOS032961918
FS-9494

2D Structure

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2D Structure of Pterisolic acid D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9788 97.88%
Caco-2 + 0.5553 55.53%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7538 75.38%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.8891 88.91%
OATP1B3 inhibitior + 0.9103 91.03%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7821 78.21%
BSEP inhibitior - 0.7948 79.48%
P-glycoprotein inhibitior - 0.8689 86.89%
P-glycoprotein substrate - 0.6725 67.25%
CYP3A4 substrate + 0.6497 64.97%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate - 0.8514 85.14%
CYP3A4 inhibition - 0.8726 87.26%
CYP2C9 inhibition - 0.8653 86.53%
CYP2C19 inhibition - 0.9177 91.77%
CYP2D6 inhibition - 0.9773 97.73%
CYP1A2 inhibition - 0.7156 71.56%
CYP2C8 inhibition - 0.8425 84.25%
CYP inhibitory promiscuity - 0.9904 99.04%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6602 66.02%
Eye corrosion - 0.9937 99.37%
Eye irritation - 0.9224 92.24%
Skin irritation + 0.6945 69.45%
Skin corrosion - 0.8908 89.08%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7859 78.59%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5467 54.67%
skin sensitisation - 0.8626 86.26%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 1.0000 100.00%
Nephrotoxicity - 0.5987 59.87%
Acute Oral Toxicity (c) II 0.3910 39.10%
Estrogen receptor binding + 0.8367 83.67%
Androgen receptor binding + 0.6960 69.60%
Thyroid receptor binding + 0.6812 68.12%
Glucocorticoid receptor binding + 0.7219 72.19%
Aromatase binding + 0.5933 59.33%
PPAR gamma - 0.5550 55.50%
Honey bee toxicity - 0.9568 95.68%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9883 98.83%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.95% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.70% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.82% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.45% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.10% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.50% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.41% 99.23%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.73% 93.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.43% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.63% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.00% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.88% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.20% 100.00%

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.
Pteris semipinnata

Cross-Links

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PubChem 53238560
LOTUS LTS0187192
wikiData Q105134379