(4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl) benzoate

Details

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Internal ID 4d746841-5200-4d3b-ac86-a6ed81bdc810
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl) benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H34O5/c1-16-18-11-14-31-20(18)15-19-21(16)22(28)23(32-24(29)17-9-6-5-7-10-17)27(30)25(2,3)12-8-13-26(19,27)4/h5-7,9-11,14,16,19,21-23,28,30H,8,12-13,15H2,1-4H3
InChI Key YMUSGWGTHSRGHT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H34O5
Molecular Weight 438.60 g/mol
Exact Mass 438.24062418 g/mol
Topological Polar Surface Area (TPSA) 79.90 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.72
H-Bond Acceptor 5
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 (4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl) benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9583 95.83%
Caco-2 + 0.5642 56.42%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7587 75.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8538 85.38%
OATP1B3 inhibitior + 0.8503 85.03%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6821 68.21%
BSEP inhibitior - 0.5560 55.60%
P-glycoprotein inhibitior + 0.5895 58.95%
P-glycoprotein substrate - 0.6505 65.05%
CYP3A4 substrate + 0.6911 69.11%
CYP2C9 substrate - 0.8133 81.33%
CYP2D6 substrate - 0.8183 81.83%
CYP3A4 inhibition - 0.6090 60.90%
CYP2C9 inhibition - 0.6503 65.03%
CYP2C19 inhibition - 0.6649 66.49%
CYP2D6 inhibition - 0.9242 92.42%
CYP1A2 inhibition + 0.5792 57.92%
CYP2C8 inhibition + 0.6968 69.68%
CYP inhibitory promiscuity - 0.7965 79.65%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6172 61.72%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.9540 95.40%
Skin irritation - 0.6651 66.51%
Skin corrosion - 0.9308 93.08%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8081 80.81%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5322 53.22%
skin sensitisation - 0.8896 88.96%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7302 73.02%
Acute Oral Toxicity (c) III 0.4609 46.09%
Estrogen receptor binding + 0.6481 64.81%
Androgen receptor binding + 0.7056 70.56%
Thyroid receptor binding + 0.5842 58.42%
Glucocorticoid receptor binding + 0.7537 75.37%
Aromatase binding + 0.7269 72.69%
PPAR gamma + 0.5602 56.02%
Honey bee toxicity - 0.8380 83.80%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9967 99.67%

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 96.38% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.16% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 95.61% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.29% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.81% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.31% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.99% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.87% 85.14%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 90.85% 87.67%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 90.05% 83.00%
CHEMBL4208 P20618 Proteasome component C5 87.99% 90.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.17% 97.25%
CHEMBL4267 P37173 TGF-beta receptor type II 86.75% 88.18%
CHEMBL1951 P21397 Monoamine oxidase A 86.27% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.94% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.41% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.43% 97.09%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 84.08% 92.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.29% 89.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.08% 93.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.91% 81.11%
CHEMBL2535 P11166 Glucose transporter 81.70% 98.75%
CHEMBL340 P08684 Cytochrome P450 3A4 81.30% 91.19%
CHEMBL226 P30542 Adenosine A1 receptor 81.12% 95.93%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.13% 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.
Caesalpinia pulcherrima

Cross-Links

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PubChem 78297420
LOTUS LTS0009852
wikiData Q105350756