Teucmosin

Details

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Internal ID 657708e3-a281-424d-a866-7cbb7f35482e
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (1S,3aR,4R,6aS)-6a-methyl-1-(3-oxobutyl)-4-propan-2-yl-3a,4,5,6-tetrahydro-1H-cyclopenta[c]furan-3-one
SMILES (Canonical) CC(C)C1CCC2(C1C(=O)OC2CCC(=O)C)C
SMILES (Isomeric) CC(C)[C@H]1CC[C@]2([C@@H]1C(=O)O[C@H]2CCC(=O)C)C
InChI InChI=1S/C15H24O3/c1-9(2)11-7-8-15(4)12(6-5-10(3)16)18-14(17)13(11)15/h9,11-13H,5-8H2,1-4H3/t11-,12+,13+,15-/m1/s1
InChI Key UKWYLUIBBUASGL-UKTARXLSSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24O3
Molecular Weight 252.35 g/mol
Exact Mass 252.17254462 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Teucmosin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.7471 74.71%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7118 71.18%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9042 90.42%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.8131 81.31%
P-glycoprotein inhibitior - 0.7540 75.40%
P-glycoprotein substrate - 0.8221 82.21%
CYP3A4 substrate + 0.5921 59.21%
CYP2C9 substrate - 0.6017 60.17%
CYP2D6 substrate - 0.8384 83.84%
CYP3A4 inhibition - 0.8861 88.61%
CYP2C9 inhibition - 0.8868 88.68%
CYP2C19 inhibition - 0.8181 81.81%
CYP2D6 inhibition - 0.9614 96.14%
CYP1A2 inhibition - 0.8650 86.50%
CYP2C8 inhibition - 0.9549 95.49%
CYP inhibitory promiscuity - 0.9721 97.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7071 70.71%
Eye corrosion - 0.9461 94.61%
Eye irritation - 0.7172 71.72%
Skin irritation - 0.5671 56.71%
Skin corrosion - 0.7578 75.78%
Ames mutagenesis - 0.7723 77.23%
Human Ether-a-go-go-Related Gene inhibition - 0.6078 60.78%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7076 70.76%
skin sensitisation - 0.5815 58.15%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6603 66.03%
Acute Oral Toxicity (c) III 0.7526 75.26%
Estrogen receptor binding + 0.5463 54.63%
Androgen receptor binding + 0.5562 55.62%
Thyroid receptor binding - 0.5502 55.02%
Glucocorticoid receptor binding - 0.6214 62.14%
Aromatase binding - 0.8313 83.13%
PPAR gamma - 0.6854 68.54%
Honey bee toxicity - 0.8784 87.84%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9636 96.36%

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 95.35% 96.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 94.45% 96.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.82% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.95% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.98% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.42% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 88.37% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.97% 99.23%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.78% 96.47%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.44% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.27% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.23% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.83% 90.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.73% 97.09%
CHEMBL1829 O15379 Histone deacetylase 3 82.59% 95.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.34% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 80.24% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.01% 94.33%

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.
Teucrium ramosissimum

Cross-Links

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PubChem 44512746
LOTUS LTS0256149
wikiData Q105274949