Stereumin J

Details

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Internal ID d3eea5a9-531f-4045-81c9-e2029f7bc764
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1S,3aS,4S,6S,6aR,9S,9aR,9bR)-6,9-dimethyl-3-methylidene-1,2,4,5,6,6a,7,8,9a,9b-decahydrophenalene-1,3a,4,9-tetrol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H26O4/c1-8-6-12(18)16(20)9(2)7-11(17)14-13(16)10(8)4-5-15(14,3)19/h8,10-14,17-20H,2,4-7H2,1,3H3/t8-,10+,11-,12-,13+,14-,15-,16-/m0/s1
InChI Key TVNDZJKRWCJCRE-OAVDDGGCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H26O4
Molecular Weight 282.37 g/mol
Exact Mass 282.18310931 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.83
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Stereumin J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9615 96.15%
Caco-2 - 0.5905 59.05%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5100 51.00%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9213 92.13%
OATP1B3 inhibitior + 0.8948 89.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7280 72.80%
BSEP inhibitior - 0.9513 95.13%
P-glycoprotein inhibitior - 0.9346 93.46%
P-glycoprotein substrate - 0.7119 71.19%
CYP3A4 substrate + 0.5784 57.84%
CYP2C9 substrate - 0.5856 58.56%
CYP2D6 substrate - 0.7492 74.92%
CYP3A4 inhibition - 0.8090 80.90%
CYP2C9 inhibition - 0.8640 86.40%
CYP2C19 inhibition - 0.7980 79.80%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition - 0.8193 81.93%
CYP2C8 inhibition - 0.7598 75.98%
CYP inhibitory promiscuity - 0.9404 94.04%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6224 62.24%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.7955 79.55%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9154 91.54%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6670 66.70%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6574 65.74%
skin sensitisation - 0.6929 69.29%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5313 53.13%
Acute Oral Toxicity (c) I 0.4006 40.06%
Estrogen receptor binding - 0.4836 48.36%
Androgen receptor binding + 0.6879 68.79%
Thyroid receptor binding + 0.7191 71.91%
Glucocorticoid receptor binding + 0.5700 57.00%
Aromatase binding + 0.5194 51.94%
PPAR gamma - 0.7597 75.97%
Honey bee toxicity - 0.8217 82.17%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9891 98.91%

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 93.16% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.78% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.65% 92.94%
CHEMBL226 P30542 Adenosine A1 receptor 89.43% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.21% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.54% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 87.53% 90.17%
CHEMBL2581 P07339 Cathepsin D 86.95% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.85% 82.69%
CHEMBL238 Q01959 Dopamine transporter 84.50% 95.88%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.48% 97.25%
CHEMBL1871 P10275 Androgen Receptor 81.89% 96.43%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.27% 86.00%

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 139585187
LOTUS LTS0175976
wikiData Q105265415