(2R,3aS,4'aR,7S,7'R,9aS,9bR)-7,7'-bis(2-hydroxypropan-2-yl)-1',4'a,5,9a-tetramethylspiro[3a,6,7,8,9,9b-hexahydrobenzo[g][1]benzofuran-2,3'-5,6,7,8-tetrahydro-4H-naphthalene]-2',3,4-trione

Details

Top
Internal ID c4db4db8-8b14-4fb9-85e4-04cd784f2189
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2R,3aS,4'aR,7S,7'R,9aS,9bR)-7,7'-bis(2-hydroxypropan-2-yl)-1',4'a,5,9a-tetramethylspiro[3a,6,7,8,9,9b-hexahydrobenzo[g][1]benzofuran-2,3'-5,6,7,8-tetrahydro-4H-naphthalene]-2',3,4-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H44O6/c1-16-21-14-19(28(5,6)36)10-12-30(21,8)26-22(23(16)32)25(34)31(37-26)15-29(7)11-9-18(27(3,4)35)13-20(29)17(2)24(31)33/h18-19,22,26,35-36H,9-15H2,1-8H3/t18-,19+,22+,26-,29-,30+,31+/m1/s1
InChI Key SKUVBRVOKSCXDJ-LYKVPTNKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C31H44O6
Molecular Weight 512.70 g/mol
Exact Mass 512.31378912 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.65
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2R,3aS,4'aR,7S,7'R,9aS,9bR)-7,7'-bis(2-hydroxypropan-2-yl)-1',4'a,5,9a-tetramethylspiro[3a,6,7,8,9,9b-hexahydrobenzo[g][1]benzofuran-2,3'-5,6,7,8-tetrahydro-4H-naphthalene]-2',3,4-trione

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 - 0.5778 57.78%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8263 82.63%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8790 87.90%
OATP1B3 inhibitior + 0.8903 89.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.7083 70.83%
BSEP inhibitior + 0.9063 90.63%
P-glycoprotein inhibitior + 0.6682 66.82%
P-glycoprotein substrate - 0.7257 72.57%
CYP3A4 substrate + 0.6482 64.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8785 87.85%
CYP3A4 inhibition - 0.7618 76.18%
CYP2C9 inhibition - 0.8043 80.43%
CYP2C19 inhibition - 0.8657 86.57%
CYP2D6 inhibition - 0.9440 94.40%
CYP1A2 inhibition - 0.6194 61.94%
CYP2C8 inhibition + 0.5078 50.78%
CYP inhibitory promiscuity - 0.8589 85.89%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4835 48.35%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.8978 89.78%
Skin irritation + 0.5866 58.66%
Skin corrosion - 0.9075 90.75%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4780 47.80%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7716 77.16%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.7195 71.95%
Acute Oral Toxicity (c) III 0.3967 39.67%
Estrogen receptor binding + 0.7337 73.37%
Androgen receptor binding + 0.7502 75.02%
Thyroid receptor binding + 0.6089 60.89%
Glucocorticoid receptor binding + 0.7914 79.14%
Aromatase binding + 0.7222 72.22%
PPAR gamma + 0.6472 64.72%
Honey bee toxicity - 0.7978 79.78%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9928 99.28%

Targets

Top

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 94.32% 91.11%
CHEMBL1871 P10275 Androgen Receptor 93.70% 96.43%
CHEMBL2581 P07339 Cathepsin D 90.69% 98.95%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 89.21% 90.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.23% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.04% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.96% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.77% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.30% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.88% 97.09%
CHEMBL1902 P62942 FK506-binding protein 1A 85.99% 97.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.95% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.19% 93.04%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 82.66% 96.90%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.41% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.15% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.82% 96.61%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 80.72% 92.95%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.47% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.45% 97.14%

Plants that contains it

Top
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.
Carissa spinarum

Cross-Links

Top
PubChem 160863620
LOTUS LTS0094023
wikiData Q105255049