(2S,4aS,10aS)-2,5-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one

Details

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Internal ID 7585249a-288b-499d-93a1-fa6e8340ae52
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (2S,4aS,10aS)-2,5-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one
SMILES (Canonical) CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(C3(C)C)O)C)O)OC
SMILES (Isomeric) CC(C)C1=C(C(=C2C(=C1)C(=O)C[C@H]3[C@@]2(CC[C@@H](C3(C)C)O)C)O)OC
InChI InChI=1S/C21H30O4/c1-11(2)12-9-13-14(22)10-15-20(3,4)16(23)7-8-21(15,5)17(13)18(24)19(12)25-6/h9,11,15-16,23-24H,7-8,10H2,1-6H3/t15-,16+,21+/m1/s1
InChI Key RBOFUIKHKQRVJQ-XFQAVAEZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O4
Molecular Weight 346.50 g/mol
Exact Mass 346.21440943 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,4aS,10aS)-2,5-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.6654 66.54%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8713 87.13%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.8782 87.82%
OATP1B3 inhibitior + 0.8755 87.55%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8071 80.71%
BSEP inhibitior - 0.5605 56.05%
P-glycoprotein inhibitior - 0.8071 80.71%
P-glycoprotein substrate - 0.7286 72.86%
CYP3A4 substrate + 0.6595 65.95%
CYP2C9 substrate - 0.5905 59.05%
CYP2D6 substrate - 0.7032 70.32%
CYP3A4 inhibition - 0.5268 52.68%
CYP2C9 inhibition - 0.7759 77.59%
CYP2C19 inhibition - 0.7739 77.39%
CYP2D6 inhibition - 0.9364 93.64%
CYP1A2 inhibition + 0.8760 87.60%
CYP2C8 inhibition - 0.7197 71.97%
CYP inhibitory promiscuity - 0.9276 92.76%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6560 65.60%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.7490 74.90%
Skin irritation - 0.5677 56.77%
Skin corrosion - 0.9533 95.33%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6585 65.85%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5834 58.34%
skin sensitisation - 0.8647 86.47%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8511 85.11%
Acute Oral Toxicity (c) III 0.6162 61.62%
Estrogen receptor binding + 0.6993 69.93%
Androgen receptor binding - 0.5865 58.65%
Thyroid receptor binding + 0.6329 63.29%
Glucocorticoid receptor binding + 0.7407 74.07%
Aromatase binding + 0.6427 64.27%
PPAR gamma + 0.7276 72.76%
Honey bee toxicity - 0.7278 72.78%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9898 98.98%

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 98.45% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.11% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.98% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.88% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.61% 96.77%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.50% 85.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.81% 82.69%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.55% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.81% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.95% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.66% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.69% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 88.25% 94.75%
CHEMBL340 P08684 Cytochrome P450 3A4 87.67% 91.19%
CHEMBL1907 P15144 Aminopeptidase N 87.64% 93.31%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.94% 92.88%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.92% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.22% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.34% 94.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.13% 93.03%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.11% 93.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.78% 95.89%
CHEMBL2535 P11166 Glucose transporter 83.27% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.16% 99.23%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.92% 96.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.41% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.21% 92.62%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.41% 90.24%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.31% 91.07%

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.
Torreya nucifera

Cross-Links

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PubChem 162911446
LOTUS LTS0135058
wikiData Q105233218