Dahliane G

Details

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Internal ID 70cbfa29-f561-4bd0-82a9-862bb06c2bad
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name [(1S,2S,3R,3aR,5aR)-1,2-dihydroxy-3a,5a-dimethyl-8-oxo-3-propan-2-yl-2,3,4,5,6,7-hexahydro-1H-benzo[f]azulen-9-yl]methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H32O5/c1-12(2)18-20(26)19(25)16-10-15-14(11-27-13(3)23)17(24)6-7-21(15,4)8-9-22(16,18)5/h10,12,18-20,25-26H,6-9,11H2,1-5H3/t18-,19-,20-,21-,22-/m0/s1
InChI Key VLKWNDNCESOJPC-YFNVTMOMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32O5
Molecular Weight 376.50 g/mol
Exact Mass 376.22497412 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dahliane G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9677 96.77%
Caco-2 + 0.6190 61.90%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8958 89.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8794 87.94%
OATP1B3 inhibitior + 0.8965 89.65%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6452 64.52%
P-glycoprotein inhibitior - 0.6526 65.26%
P-glycoprotein substrate - 0.7281 72.81%
CYP3A4 substrate + 0.6389 63.89%
CYP2C9 substrate - 0.7791 77.91%
CYP2D6 substrate - 0.8980 89.80%
CYP3A4 inhibition - 0.9081 90.81%
CYP2C9 inhibition - 0.6154 61.54%
CYP2C19 inhibition - 0.8532 85.32%
CYP2D6 inhibition - 0.9378 93.78%
CYP1A2 inhibition - 0.6336 63.36%
CYP2C8 inhibition - 0.7437 74.37%
CYP inhibitory promiscuity - 0.9324 93.24%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6304 63.04%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9266 92.66%
Skin irritation + 0.5490 54.90%
Skin corrosion - 0.9545 95.45%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7175 71.75%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.6393 63.93%
skin sensitisation - 0.8531 85.31%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6413 64.13%
Acute Oral Toxicity (c) III 0.6028 60.28%
Estrogen receptor binding + 0.6831 68.31%
Androgen receptor binding + 0.5564 55.64%
Thyroid receptor binding + 0.6054 60.54%
Glucocorticoid receptor binding + 0.7768 77.68%
Aromatase binding + 0.6848 68.48%
PPAR gamma + 0.6296 62.96%
Honey bee toxicity - 0.7902 79.02%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9957 99.57%

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 98.75% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.60% 97.25%
CHEMBL2581 P07339 Cathepsin D 97.04% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.87% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.27% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.38% 85.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.44% 96.77%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.37% 82.69%
CHEMBL221 P23219 Cyclooxygenase-1 88.04% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.41% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.28% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 84.18% 91.19%
CHEMBL226 P30542 Adenosine A1 receptor 83.31% 95.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.83% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.47% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.44% 100.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 81.17% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.66% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.46% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 146683330
LOTUS LTS0081481
wikiData Q105288472