(1S,4S,8S,10S)-4-(2-hydroxypropan-2-yl)-9,9-dimethyl-8,10-bis(3-methylbut-2-enyl)-1-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.02,6]dodec-2(6)-ene-5,12-dione

Details

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Internal ID bd067026-8843-4dd0-b57b-46e93324c61f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids
IUPAC Name (1S,4S,8S,10S)-4-(2-hydroxypropan-2-yl)-9,9-dimethyl-8,10-bis(3-methylbut-2-enyl)-1-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.02,6]dodec-2(6)-ene-5,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H44O5/c1-17(2)11-12-20-15-30(23(32)19(5)6)24-21(22(31)25(35-24)28(9,10)34)16-29(26(30)33,27(20,7)8)14-13-18(3)4/h11,13,19-20,25,34H,12,14-16H2,1-10H3/t20-,25+,29+,30+/m0/s1
InChI Key XASFDRCVNCHCNC-BJKZPFNHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H44O5
Molecular Weight 484.70 g/mol
Exact Mass 484.31887450 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 6.40
Atomic LogP (AlogP) 5.91
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4S,8S,10S)-4-(2-hydroxypropan-2-yl)-9,9-dimethyl-8,10-bis(3-methylbut-2-enyl)-1-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.02,6]dodec-2(6)-ene-5,12-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 - 0.5276 52.76%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7289 72.89%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8717 87.17%
OATP1B3 inhibitior + 0.9098 90.98%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6581 65.81%
P-glycoprotein inhibitior - 0.4635 46.35%
P-glycoprotein substrate + 0.5056 50.56%
CYP3A4 substrate + 0.6493 64.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8693 86.93%
CYP3A4 inhibition - 0.9060 90.60%
CYP2C9 inhibition - 0.7451 74.51%
CYP2C19 inhibition - 0.8411 84.11%
CYP2D6 inhibition - 0.9270 92.70%
CYP1A2 inhibition - 0.6497 64.97%
CYP2C8 inhibition - 0.7247 72.47%
CYP inhibitory promiscuity - 0.6061 60.61%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4474 44.74%
Eye corrosion - 0.9832 98.32%
Eye irritation - 0.8731 87.31%
Skin irritation - 0.5125 51.25%
Skin corrosion - 0.9109 91.09%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5552 55.52%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.6054 60.54%
skin sensitisation - 0.6174 61.74%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5737 57.37%
Acute Oral Toxicity (c) III 0.5580 55.80%
Estrogen receptor binding + 0.6706 67.06%
Androgen receptor binding + 0.6440 64.40%
Thyroid receptor binding + 0.6320 63.20%
Glucocorticoid receptor binding + 0.6509 65.09%
Aromatase binding + 0.5913 59.13%
PPAR gamma + 0.7198 71.98%
Honey bee toxicity - 0.8083 80.83%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9864 98.64%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.03% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.64% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.96% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.17% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 93.86% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.34% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.28% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.33% 96.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.32% 91.07%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.65% 89.34%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.64% 90.08%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.66% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.45% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.34% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.69% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.68% 92.62%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.24% 95.71%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.03% 92.88%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.76% 89.50%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 80.57% 82.50%
CHEMBL2842 P42345 Serine/threonine-protein kinase mTOR 80.36% 92.78%

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.
Garcinia subelliptica

Cross-Links

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PubChem 162821324
LOTUS LTS0109815
wikiData Q105324095