Radianspene A

Details

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Internal ID 16088b97-8540-4520-b83c-c796433a9fc9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name [(1S,2R,3R,3aR,5aR)-1-hydroxy-9-(hydroxymethyl)-3a,5a-dimethyl-8-oxo-3-propan-2-yl-2,3,4,5,6,7-hexahydro-1H-benzo[f]azulen-2-yl] acetate
SMILES (Canonical) CC(C)C1C(C(C2=CC3=C(C(=O)CCC3(CCC12C)C)CO)O)OC(=O)C
SMILES (Isomeric) CC(C)[C@H]1[C@H]([C@H](C2=CC3=C(C(=O)CC[C@]3(CC[C@]12C)C)CO)O)OC(=O)C
InChI InChI=1S/C22H32O5/c1-12(2)18-20(27-13(3)24)19(26)16-10-15-14(11-23)17(25)6-7-21(15,4)8-9-22(16,18)5/h10,12,18-20,23,26H,6-9,11H2,1-5H3/t18-,19-,20+,21-,22-/m0/s1
InChI Key BEMZAUOOVKSYLX-CUUWFGFTSA-N
Popularity 1 reference 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 2.70
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 Radianspene A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9775 97.75%
Caco-2 + 0.6459 64.59%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8762 87.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8550 85.50%
OATP1B3 inhibitior + 0.8638 86.38%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5593 55.93%
BSEP inhibitior + 0.5623 56.23%
P-glycoprotein inhibitior - 0.5820 58.20%
P-glycoprotein substrate - 0.6896 68.96%
CYP3A4 substrate + 0.6396 63.96%
CYP2C9 substrate - 0.7976 79.76%
CYP2D6 substrate - 0.9044 90.44%
CYP3A4 inhibition - 0.8526 85.26%
CYP2C9 inhibition - 0.6172 61.72%
CYP2C19 inhibition - 0.8991 89.91%
CYP2D6 inhibition - 0.9393 93.93%
CYP1A2 inhibition - 0.7212 72.12%
CYP2C8 inhibition - 0.8213 82.13%
CYP inhibitory promiscuity - 0.8942 89.42%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6366 63.66%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9402 94.02%
Skin irritation + 0.5834 58.34%
Skin corrosion - 0.9589 95.89%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6577 65.77%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5483 54.83%
skin sensitisation - 0.8867 88.67%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7586 75.86%
Acute Oral Toxicity (c) III 0.6996 69.96%
Estrogen receptor binding + 0.6354 63.54%
Androgen receptor binding + 0.5321 53.21%
Thyroid receptor binding + 0.5809 58.09%
Glucocorticoid receptor binding + 0.8058 80.58%
Aromatase binding + 0.5964 59.64%
PPAR gamma + 0.5516 55.16%
Honey bee toxicity - 0.7735 77.35%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9910 99.10%

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 98.54% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.50% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.91% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.67% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.55% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.80% 85.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.12% 82.69%
CHEMBL226 P30542 Adenosine A1 receptor 86.76% 95.93%
CHEMBL340 P08684 Cytochrome P450 3A4 85.10% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.89% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.45% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.40% 95.89%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.65% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.43% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 82.27% 94.75%
CHEMBL5028 O14672 ADAM10 80.95% 97.50%
CHEMBL4208 P20618 Proteasome component C5 80.26% 90.00%

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 101585004
LOTUS LTS0253349
wikiData Q77573827