(1S,4R,4aS,5R,7R,7aS,8S,9R,11aS)-8-(1H-indol-3-yl)-4,4a,7-trimethyl-9-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,8,9,10,11-dodecahydrobenzo[d]naphthalene-1,5-diol

Details

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Internal ID 52379d42-0031-4ba1-a672-5069d17fcd6e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,4R,4aS,5R,7R,7aS,8S,9R,11aS)-8-(1H-indol-3-yl)-4,4a,7-trimethyl-9-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,8,9,10,11-dodecahydrobenzo[d]naphthalene-1,5-diol
SMILES (Canonical) CC1CCC(C23C1(C(CC(C2C(C(CC3)C(=C)C)C4=CNC5=CC=CC=C54)C)O)C)O
SMILES (Isomeric) C[C@@H]1CC[C@@H]([C@]23[C@]1([C@@H](C[C@H]([C@H]2[C@H]([C@@H](CC3)C(=C)C)C4=CNC5=CC=CC=C54)C)O)C)O
InChI InChI=1S/C28H39NO2/c1-16(2)19-12-13-28-23(30)11-10-18(4)27(28,5)24(31)14-17(3)26(28)25(19)21-15-29-22-9-7-6-8-20(21)22/h6-9,15,17-19,23-26,29-31H,1,10-14H2,2-5H3/t17-,18-,19+,23+,24-,25-,26+,27-,28+/m1/s1
InChI Key KHMAONVROPNUDX-PHLGNYFESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H39NO2
Molecular Weight 421.60 g/mol
Exact Mass 421.298079487 g/mol
Topological Polar Surface Area (TPSA) 56.20 Ų
XlogP 6.30
Atomic LogP (AlogP) 6.04
H-Bond Acceptor 2
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4R,4aS,5R,7R,7aS,8S,9R,11aS)-8-(1H-indol-3-yl)-4,4a,7-trimethyl-9-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,8,9,10,11-dodecahydrobenzo[d]naphthalene-1,5-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5370 53.70%
Blood Brain Barrier - 0.5371 53.71%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.4091 40.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.9166 91.66%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8875 88.75%
P-glycoprotein inhibitior - 0.5892 58.92%
P-glycoprotein substrate + 0.6999 69.99%
CYP3A4 substrate + 0.6990 69.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3578 35.78%
CYP3A4 inhibition + 0.6422 64.22%
CYP2C9 inhibition - 0.7526 75.26%
CYP2C19 inhibition + 0.6234 62.34%
CYP2D6 inhibition - 0.8751 87.51%
CYP1A2 inhibition + 0.7095 70.95%
CYP2C8 inhibition + 0.6887 68.87%
CYP inhibitory promiscuity + 0.7604 76.04%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.4903 49.03%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.9511 95.11%
Skin irritation - 0.7222 72.22%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8425 84.25%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.7946 79.46%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.7259 72.59%
Acute Oral Toxicity (c) III 0.5775 57.75%
Estrogen receptor binding + 0.7433 74.33%
Androgen receptor binding + 0.7590 75.90%
Thyroid receptor binding + 0.6633 66.33%
Glucocorticoid receptor binding + 0.6894 68.94%
Aromatase binding + 0.7566 75.66%
PPAR gamma - 0.5837 58.37%
Honey bee toxicity - 0.8447 84.47%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9886 98.86%

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 99.09% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.23% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 94.27% 97.79%
CHEMBL1951 P21397 Monoamine oxidase A 89.14% 91.49%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 89.08% 92.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.53% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.75% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.57% 89.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.28% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.05% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.44% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.29% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.18% 94.45%
CHEMBL5028 O14672 ADAM10 83.46% 97.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.27% 92.62%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.88% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.76% 86.33%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.21% 100.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.16% 94.62%

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.
There are no matching plants.

Cross-Links

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PubChem 124511202
LOTUS LTS0254388
wikiData Q105141218