(2Z)-2-[(1R,3R,5R,6S,10R)-1,6-dihydroxy-10-(3-hydroxypropyl)-6-methyl-3-[(1E,3E)-2-methyl-4-[(5S)-2,5,6,6-tetramethylcyclohexen-1-yl]buta-1,3-dienyl]-2-oxaspiro[4.5]decan-9-ylidene]propanal

Details

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Internal ID dfa6bc34-df1d-4244-b311-9667254e65eb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2Z)-2-[(1R,3R,5R,6S,10R)-1,6-dihydroxy-10-(3-hydroxypropyl)-6-methyl-3-[(1E,3E)-2-methyl-4-[(5S)-2,5,6,6-tetramethylcyclohexen-1-yl]buta-1,3-dienyl]-2-oxaspiro[4.5]decan-9-ylidene]propanal
SMILES (Canonical) CC1CCC(=C(C1(C)C)C=CC(=CC2CC3(C(C(=C(C)C=O)CCC3(C)O)CCCO)C(O2)O)C)C
SMILES (Isomeric) C[C@H]1CCC(=C(C1(C)C)/C=C/C(=C/[C@H]2C[C@]3([C@@H](/C(=C(/C)\C=O)/CC[C@]3(C)O)CCCO)[C@@H](O2)O)/C)C
InChI InChI=1S/C31H48O5/c1-20(10-13-26-21(2)11-12-23(4)29(26,5)6)17-24-18-31(28(34)36-24)27(9-8-16-32)25(22(3)19-33)14-15-30(31,7)35/h10,13,17,19,23-24,27-28,32,34-35H,8-9,11-12,14-16,18H2,1-7H3/b13-10+,20-17+,25-22-/t23-,24-,27+,28+,30-,31-/m0/s1
InChI Key VKLHLMJHQATABJ-KRVAJWFPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H48O5
Molecular Weight 500.70 g/mol
Exact Mass 500.35017463 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 5.80
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2Z)-2-[(1R,3R,5R,6S,10R)-1,6-dihydroxy-10-(3-hydroxypropyl)-6-methyl-3-[(1E,3E)-2-methyl-4-[(5S)-2,5,6,6-tetramethylcyclohexen-1-yl]buta-1,3-dienyl]-2-oxaspiro[4.5]decan-9-ylidene]propanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9611 96.11%
Caco-2 - 0.6578 65.78%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7530 75.30%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.8528 85.28%
OATP1B3 inhibitior + 0.9043 90.43%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5609 56.09%
BSEP inhibitior + 0.9801 98.01%
P-glycoprotein inhibitior + 0.7655 76.55%
P-glycoprotein substrate + 0.6082 60.82%
CYP3A4 substrate + 0.7145 71.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8649 86.49%
CYP3A4 inhibition - 0.7300 73.00%
CYP2C9 inhibition - 0.8262 82.62%
CYP2C19 inhibition - 0.8932 89.32%
CYP2D6 inhibition - 0.9378 93.78%
CYP1A2 inhibition - 0.9107 91.07%
CYP2C8 inhibition + 0.6160 61.60%
CYP inhibitory promiscuity - 0.8452 84.52%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6047 60.47%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9533 95.33%
Skin irritation + 0.4936 49.36%
Skin corrosion - 0.9495 94.95%
Ames mutagenesis + 0.5230 52.30%
Human Ether-a-go-go-Related Gene inhibition + 0.6839 68.39%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5994 59.94%
skin sensitisation - 0.8585 85.85%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.7138 71.38%
Acute Oral Toxicity (c) III 0.5051 50.51%
Estrogen receptor binding + 0.7594 75.94%
Androgen receptor binding + 0.7293 72.93%
Thyroid receptor binding + 0.6395 63.95%
Glucocorticoid receptor binding + 0.8289 82.89%
Aromatase binding + 0.7706 77.06%
PPAR gamma + 0.5182 51.82%
Honey bee toxicity - 0.7982 79.82%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9796 97.96%

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 95.88% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.80% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.72% 100.00%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 92.29% 95.52%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.15% 95.56%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 88.63% 95.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.99% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.74% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.72% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.60% 98.95%
CHEMBL5555 O00767 Acyl-CoA desaturase 83.66% 97.50%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 83.03% 89.05%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.00% 91.71%
CHEMBL2996 Q05655 Protein kinase C delta 82.54% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.97% 97.09%
CHEMBL1870 P28702 Retinoid X receptor beta 80.23% 95.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.01% 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.
Iris hoogiana

Cross-Links

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PubChem 162981459
LOTUS LTS0209431
wikiData Q104667784