(1R,2R,5R,6R,9R,10R,13S,15S)-5-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-2,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol

Details

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Internal ID bfc641e6-5847-473a-b120-d7d333e819f3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2R,5R,6R,9R,10R,13S,15S)-5-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-2,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol
SMILES (Canonical) CC(C)C(C)C=CC(C)C1CCC2(C1CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C
SMILES (Isomeric) C[C@H](/C=C/[C@@H](C)C(C)C)[C@H]1CC[C@@]2([C@@H]1CC[C@H]3[C@]24C=C[C@@]5([C@@]3(CC[C@@H](C5)O)C)OO4)C
InChI InChI=1S/C28H44O3/c1-18(2)19(3)7-8-20(4)22-12-14-25(5)23(22)9-10-24-26(6)13-11-21(29)17-27(26)15-16-28(24,25)31-30-27/h7-8,15-16,18-24,29H,9-14,17H2,1-6H3/b8-7+/t19-,20-,21+,22-,23-,24-,25-,26-,27-,28-/m1/s1
InChI Key GRGWPUZWMHKISD-ASHKMTMBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H44O3
Molecular Weight 428.60 g/mol
Exact Mass 428.32904526 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 6.70
Atomic LogP (AlogP) 6.47
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2R,5R,6R,9R,10R,13S,15S)-5-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-2,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.5060 50.60%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4777 47.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8478 84.78%
OATP1B3 inhibitior + 0.9007 90.07%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7569 75.69%
P-glycoprotein inhibitior - 0.4603 46.03%
P-glycoprotein substrate - 0.6594 65.94%
CYP3A4 substrate + 0.6693 66.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7078 70.78%
CYP3A4 inhibition - 0.8935 89.35%
CYP2C9 inhibition - 0.8688 86.88%
CYP2C19 inhibition - 0.8361 83.61%
CYP2D6 inhibition - 0.9469 94.69%
CYP1A2 inhibition - 0.7562 75.62%
CYP2C8 inhibition - 0.6161 61.61%
CYP inhibitory promiscuity - 0.9601 96.01%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5951 59.51%
Eye corrosion - 0.9776 97.76%
Eye irritation - 0.9527 95.27%
Skin irritation - 0.6652 66.52%
Skin corrosion - 0.9168 91.68%
Ames mutagenesis - 0.6234 62.34%
Human Ether-a-go-go-Related Gene inhibition + 0.6960 69.60%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5806 58.06%
skin sensitisation - 0.6921 69.21%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8183 81.83%
Acute Oral Toxicity (c) III 0.4103 41.03%
Estrogen receptor binding + 0.8352 83.52%
Androgen receptor binding + 0.7540 75.40%
Thyroid receptor binding + 0.6786 67.86%
Glucocorticoid receptor binding + 0.7342 73.42%
Aromatase binding + 0.6054 60.54%
PPAR gamma + 0.5482 54.82%
Honey bee toxicity - 0.6406 64.06%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8695 86.95%

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 95.89% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.28% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 93.94% 95.93%
CHEMBL4072 P07858 Cathepsin B 90.23% 93.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.34% 95.89%
CHEMBL3837 P07711 Cathepsin L 88.45% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.44% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 87.34% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.00% 93.56%
CHEMBL2179 P04062 Beta-glucocerebrosidase 86.31% 85.31%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.20% 97.14%
CHEMBL1937 Q92769 Histone deacetylase 2 85.56% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.24% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.29% 82.69%
CHEMBL5203 P33316 dUTP pyrophosphatase 83.77% 99.18%
CHEMBL268 P43235 Cathepsin K 83.15% 96.85%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.97% 96.61%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.56% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.06% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.87% 89.00%

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.
Bauhinia purpurea

Cross-Links

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PubChem 162932005
LOTUS LTS0161679
wikiData Q105015915