Stereumin T

Details

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Internal ID edba988b-8431-4a32-bd3c-39f9d9cdf8b2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(3aR,5S,5aR,9S,9aR,9bS)-3a,9b-dihydroxy-5,8-dimethyl-1-methylidene-4,5,5a,6,9,9a-hexahydrobenzo[e][1]benzofuran-9-yl] octanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H36O5/c1-5-6-7-8-9-10-19(24)28-21-15(2)11-12-18-16(3)13-22(25)23(26,20(18)21)17(4)14-27-22/h11,16,18,20-21,25-26H,4-10,12-14H2,1-3H3/t16-,18+,20+,21+,22+,23+/m0/s1
InChI Key LERUJOXQLASWHV-QQBWQSCDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H36O5
Molecular Weight 392.50 g/mol
Exact Mass 392.25627424 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.89
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Stereumin T

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9834 98.34%
Caco-2 + 0.4947 49.47%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7235 72.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8854 88.54%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7542 75.42%
BSEP inhibitior - 0.5238 52.38%
P-glycoprotein inhibitior - 0.6095 60.95%
P-glycoprotein substrate + 0.5739 57.39%
CYP3A4 substrate + 0.6490 64.90%
CYP2C9 substrate - 0.8088 80.88%
CYP2D6 substrate - 0.8767 87.67%
CYP3A4 inhibition + 0.5699 56.99%
CYP2C9 inhibition - 0.7189 71.89%
CYP2C19 inhibition - 0.7200 72.00%
CYP2D6 inhibition - 0.9264 92.64%
CYP1A2 inhibition - 0.7503 75.03%
CYP2C8 inhibition + 0.4870 48.70%
CYP inhibitory promiscuity - 0.8190 81.90%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5929 59.29%
Eye corrosion - 0.9918 99.18%
Eye irritation - 0.9516 95.16%
Skin irritation + 0.6897 68.97%
Skin corrosion - 0.9390 93.90%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6901 69.01%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.6159 61.59%
skin sensitisation - 0.8997 89.97%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5201 52.01%
Acute Oral Toxicity (c) III 0.4251 42.51%
Estrogen receptor binding + 0.6971 69.71%
Androgen receptor binding + 0.6734 67.34%
Thyroid receptor binding + 0.5407 54.07%
Glucocorticoid receptor binding + 0.7376 73.76%
Aromatase binding + 0.5933 59.33%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8500 85.00%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.8218 82.18%
Fish aquatic toxicity + 0.9962 99.62%

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 97.70% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.55% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 95.45% 89.63%
CHEMBL2581 P07339 Cathepsin D 94.49% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.21% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.38% 97.21%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.12% 93.56%
CHEMBL5255 O00206 Toll-like receptor 4 90.94% 92.50%
CHEMBL2996 Q05655 Protein kinase C delta 90.61% 97.79%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.14% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.98% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.51% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.56% 97.25%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.78% 100.00%
CHEMBL299 P17252 Protein kinase C alpha 83.63% 98.03%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.41% 100.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.10% 91.24%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.60% 89.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.60% 86.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.31% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.26% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 80.22% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 80.03% 94.73%

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 139587934
LOTUS LTS0189676
wikiData Q105150759