beta-Dictyopterol

Details

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Internal ID 51712d68-49b1-44b4-bf0b-5d07699446c7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (1R,4aS,6R,8aR)-8a-methyl-4-methylidene-6-prop-1-en-2-yl-1,2,3,4a,5,6,7,8-octahydronaphthalen-1-ol
SMILES (Canonical) CC(=C)C1CCC2(C(CCC(=C)C2C1)O)C
SMILES (Isomeric) CC(=C)[C@@H]1CC[C@]2([C@@H](CCC(=C)[C@@H]2C1)O)C
InChI InChI=1S/C15H24O/c1-10(2)12-7-8-15(4)13(9-12)11(3)5-6-14(15)16/h12-14,16H,1,3,5-9H2,2,4H3/t12-,13+,14-,15-/m1/s1
InChI Key CORHHSPHLRPKPM-LXTVHRRPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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.beta.-Dictyopterol
CORHHSPHLRPKPM-LXTVHRRPSA-N

2D Structure

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2D Structure of beta-Dictyopterol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.6704 67.04%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.5607 56.07%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.9356 93.56%
OATP1B3 inhibitior + 0.8965 89.65%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6099 60.99%
BSEP inhibitior - 0.8725 87.25%
P-glycoprotein inhibitior - 0.9503 95.03%
P-glycoprotein substrate - 0.8226 82.26%
CYP3A4 substrate + 0.6042 60.42%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.6992 69.92%
CYP2C9 inhibition - 0.8182 81.82%
CYP2C19 inhibition - 0.6124 61.24%
CYP2D6 inhibition - 0.9406 94.06%
CYP1A2 inhibition - 0.7907 79.07%
CYP2C8 inhibition - 0.8991 89.91%
CYP inhibitory promiscuity - 0.8443 84.43%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5322 53.22%
Eye corrosion - 0.9829 98.29%
Eye irritation + 0.7457 74.57%
Skin irritation + 0.5932 59.32%
Skin corrosion - 0.9291 92.91%
Ames mutagenesis - 0.8637 86.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4674 46.74%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.6626 66.26%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7365 73.65%
Acute Oral Toxicity (c) III 0.7836 78.36%
Estrogen receptor binding - 0.6324 63.24%
Androgen receptor binding - 0.5088 50.88%
Thyroid receptor binding - 0.7140 71.40%
Glucocorticoid receptor binding - 0.5998 59.98%
Aromatase binding - 0.6934 69.34%
PPAR gamma - 0.7789 77.89%
Honey bee toxicity - 0.8495 84.95%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9910 99.10%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.37% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.73% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 89.71% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.12% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.29% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.13% 97.09%
CHEMBL1871 P10275 Androgen Receptor 85.30% 96.43%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.87% 82.69%
CHEMBL1951 P21397 Monoamine oxidase A 83.21% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.35% 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.
Chrysanthemum morifolium
Curcuma zedoaria
Ligularia stenocephala

Cross-Links

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PubChem 10059334
NPASS NPC218163
LOTUS LTS0114619
wikiData Q104399170