CID 10807787

Details

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Internal ID a9bda747-cea0-42d3-867c-359b472a4443
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name
SMILES (Canonical) CC1CC(C2C(CCCC2(C13CC(=O)C4(O3)COC=C4)C)(C)CO)O
SMILES (Isomeric) C[C@@H]1C[C@H]([C@H]2[C@@](CCC[C@@]2([C@@]13CC(=O)[C@]4(O3)COC=C4)C)(C)CO)O
InChI InChI=1S/C20H30O5/c1-13-9-14(22)16-17(2,11-21)5-4-6-18(16,3)20(13)10-15(23)19(25-20)7-8-24-12-19/h7-8,13-14,16,21-22H,4-6,9-12H2,1-3H3/t13-,14-,16+,17-,18+,19-,20-/m1/s1
InChI Key MRHAMHQNBQNENT-IYIKMHAFSA-N
Popularity 1 reference 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) 76.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 10807787

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9805 98.05%
Caco-2 + 0.5454 54.54%
Blood Brain Barrier + 0.6135 61.35%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6780 67.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8321 83.21%
OATP1B3 inhibitior + 0.9395 93.95%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.5792 57.92%
BSEP inhibitior + 0.8062 80.62%
P-glycoprotein inhibitior - 0.7954 79.54%
P-glycoprotein substrate - 0.5809 58.09%
CYP3A4 substrate + 0.6248 62.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8113 81.13%
CYP3A4 inhibition - 0.8089 80.89%
CYP2C9 inhibition - 0.8876 88.76%
CYP2C19 inhibition - 0.8753 87.53%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition - 0.9111 91.11%
CYP2C8 inhibition - 0.6853 68.53%
CYP inhibitory promiscuity - 0.9401 94.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4739 47.39%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9821 98.21%
Skin irritation - 0.6024 60.24%
Skin corrosion - 0.9564 95.64%
Ames mutagenesis - 0.5324 53.24%
Human Ether-a-go-go-Related Gene inhibition - 0.4630 46.30%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5078 50.78%
skin sensitisation - 0.9061 90.61%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6196 61.96%
Acute Oral Toxicity (c) III 0.5130 51.30%
Estrogen receptor binding + 0.7882 78.82%
Androgen receptor binding + 0.7099 70.99%
Thyroid receptor binding + 0.6564 65.64%
Glucocorticoid receptor binding + 0.7014 70.14%
Aromatase binding + 0.8295 82.95%
PPAR gamma + 0.5587 55.87%
Honey bee toxicity - 0.8364 83.64%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.8486 84.86%

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 98.16% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.54% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.25% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.58% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 91.41% 94.75%
CHEMBL2581 P07339 Cathepsin D 91.35% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.34% 95.56%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.80% 96.61%
CHEMBL325 Q13547 Histone deacetylase 1 88.05% 95.92%
CHEMBL2996 Q05655 Protein kinase C delta 87.34% 97.79%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.20% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.06% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.66% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.00% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.77% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.72% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.30% 89.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.67% 93.04%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.51% 95.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.40% 95.50%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.75% 89.34%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.60% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.32% 94.00%

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.
Marrubium globosum

Cross-Links

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PubChem 10807787
LOTUS LTS0275877
wikiData Q105170568