(1R,2R,4S)-1-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(2S,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol

Details

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Internal ID a774e8ad-0387-47b3-9e65-b413475e6f0f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (1R,2R,4S)-1-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(2S,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol
SMILES (Canonical) CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=CC3(C(CC(CC3(C)O)O)(C)C)O
SMILES (Isomeric) C/C(=C\C=C\C=C(/C)\C=C\C=C(/C)\[C@@H]1C=C2[C@](O1)(C[C@H](CC2(C)C)O)C)/C=C/C=C(\C)/C=C/[C@@]3([C@](C[C@H](CC3(C)C)O)(C)O)O
InChI InChI=1S/C40H58O5/c1-28(17-13-18-30(3)21-22-40(44)37(7,8)25-33(42)27-39(40,10)43)15-11-12-16-29(2)19-14-20-31(4)34-23-35-36(5,6)24-32(41)26-38(35,9)45-34/h11-23,32-34,41-44H,24-27H2,1-10H3/b12-11+,17-13+,19-14+,22-21+,28-15+,29-16+,30-18+,31-20+/t32-,33-,34-,38+,39+,40+/m0/s1
InChI Key WWUKNXCHIOGECP-LRJXZMMBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C40H58O5
Molecular Weight 618.90 g/mol
Exact Mass 618.42842495 g/mol
Topological Polar Surface Area (TPSA) 90.20 Ų
XlogP 8.40
Atomic LogP (AlogP) 7.92
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2R,4S)-1-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(2S,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9688 96.88%
Caco-2 - 0.8331 83.31%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5466 54.66%
OATP2B1 inhibitior + 0.5747 57.47%
OATP1B1 inhibitior + 0.8578 85.78%
OATP1B3 inhibitior + 0.9563 95.63%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9888 98.88%
P-glycoprotein inhibitior + 0.7533 75.33%
P-glycoprotein substrate - 0.5145 51.45%
CYP3A4 substrate + 0.6695 66.95%
CYP2C9 substrate - 0.8102 81.02%
CYP2D6 substrate - 0.7872 78.72%
CYP3A4 inhibition - 0.8695 86.95%
CYP2C9 inhibition - 0.8246 82.46%
CYP2C19 inhibition - 0.7884 78.84%
CYP2D6 inhibition - 0.9140 91.40%
CYP1A2 inhibition - 0.8132 81.32%
CYP2C8 inhibition - 0.5699 56.99%
CYP inhibitory promiscuity - 0.7029 70.29%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4370 43.70%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9094 90.94%
Skin irritation - 0.6217 62.17%
Skin corrosion - 0.9154 91.54%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7811 78.11%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.5171 51.71%
skin sensitisation - 0.7482 74.82%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.5798 57.98%
Acute Oral Toxicity (c) I 0.4305 43.05%
Estrogen receptor binding + 0.8245 82.45%
Androgen receptor binding + 0.7237 72.37%
Thyroid receptor binding + 0.7109 71.09%
Glucocorticoid receptor binding + 0.7797 77.97%
Aromatase binding + 0.5634 56.34%
PPAR gamma + 0.7334 73.34%
Honey bee toxicity - 0.7267 72.67%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9362 93.62%

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 95.50% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.01% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 87.76% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.66% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.26% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.22% 94.45%
CHEMBL2996 Q05655 Protein kinase C delta 83.31% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.12% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.73% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 82.12% 94.75%
CHEMBL2004 P48443 Retinoid X receptor gamma 81.61% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.81% 92.94%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.50% 100.00%
CHEMBL2061 P19793 Retinoid X receptor alpha 80.05% 91.67%

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.
Rosa foetida

Cross-Links

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PubChem 162940033
LOTUS LTS0084473
wikiData Q105314329