Tetrahydrodeoxoargentamin

Details

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Internal ID 39b0ec02-bcae-41a3-aea0-4dfdc4d50643
Taxonomy Alkaloids and derivatives > Lupin alkaloids > Sparteine, lupanine, and related alkaloids
IUPAC Name 7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-ol
SMILES (Canonical) C1CCN2CC3CC(C2C1)CN4C3CC(CC4)O
SMILES (Isomeric) C1CCN2CC3CC(C2C1)CN4C3CC(CC4)O
InChI InChI=1S/C15H26N2O/c18-13-4-6-17-9-11-7-12(15(17)8-13)10-16-5-2-1-3-14(11)16/h11-15,18H,1-10H2
InChI Key MMXKVQSOWVEFOB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26N2O
Molecular Weight 250.38 g/mol
Exact Mass 250.204513457 g/mol
Topological Polar Surface Area (TPSA) 26.70 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.32
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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Spartein-4-ol #
Tetrahydrodeoxoargentamin
MMXKVQSOWVEFOB-UHFFFAOYSA-N
NSC-95095

2D Structure

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2D Structure of Tetrahydrodeoxoargentamin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.5874 58.74%
Blood Brain Barrier + 0.9194 91.94%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6930 69.30%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.9597 95.97%
OATP1B3 inhibitior + 0.9494 94.94%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.7524 75.24%
P-glycoprotein inhibitior - 0.9439 94.39%
P-glycoprotein substrate - 0.8184 81.84%
CYP3A4 substrate - 0.6068 60.68%
CYP2C9 substrate - 0.6462 64.62%
CYP2D6 substrate + 0.6764 67.64%
CYP3A4 inhibition - 0.9691 96.91%
CYP2C9 inhibition - 0.9502 95.02%
CYP2C19 inhibition - 0.9386 93.86%
CYP2D6 inhibition - 0.7550 75.50%
CYP1A2 inhibition - 0.8096 80.96%
CYP2C8 inhibition - 0.9733 97.33%
CYP inhibitory promiscuity - 0.9731 97.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9830 98.30%
Carcinogenicity (trinary) Non-required 0.6592 65.92%
Eye corrosion - 0.8453 84.53%
Eye irritation + 0.7545 75.45%
Skin irritation + 0.4906 49.06%
Skin corrosion - 0.6150 61.50%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5636 56.36%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.8564 85.64%
skin sensitisation - 0.8756 87.56%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.5541 55.41%
Acute Oral Toxicity (c) III 0.6957 69.57%
Estrogen receptor binding - 0.6919 69.19%
Androgen receptor binding - 0.5738 57.38%
Thyroid receptor binding - 0.5522 55.22%
Glucocorticoid receptor binding - 0.6455 64.55%
Aromatase binding - 0.7482 74.82%
PPAR gamma - 0.8428 84.28%
Honey bee toxicity - 0.9279 92.79%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity - 0.9747 97.47%

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
CHEMBL3023 Q9NRA0 Sphingosine kinase 2 94.36% 95.61%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.08% 97.25%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 90.94% 96.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.29% 97.09%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 87.31% 94.78%
CHEMBL237 P41145 Kappa opioid receptor 86.72% 98.10%
CHEMBL4235 P28845 11-beta-hydroxysteroid dehydrogenase 1 86.64% 97.98%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.46% 95.89%
CHEMBL238 Q01959 Dopamine transporter 86.37% 95.88%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.85% 95.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.14% 93.04%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.93% 96.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.72% 93.03%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 82.27% 98.33%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 82.08% 89.32%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 82.01% 98.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.32% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.24% 92.94%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 81.03% 98.46%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.13% 91.03%

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.
Thermopsis lanceolata

Cross-Links

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PubChem 261946
LOTUS LTS0230595
wikiData Q105168174