4-Hydroxylupanine

Details

Top
Internal ID f27fb471-5782-4102-a32a-62bced4810b5
Taxonomy Alkaloids and derivatives > Lupin alkaloids > Sparteine, lupanine, and related alkaloids
IUPAC Name (2S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-ol
SMILES (Canonical) C1CCN2CC3CC(C2C1)CN4C3CCCC4O
SMILES (Isomeric) C1CCN2CC3CC([C@H]2C1)CN4[C@H]3CCCC4O
InChI InChI=1S/C15H26N2O/c18-15-6-3-5-14-11-8-12(10-17(14)15)13-4-1-2-7-16(13)9-11/h11-15,18H,1-10H2/t11?,12?,13-,14+,15?/m1/s1
InChI Key AFEKUFYCNWZEGZ-HTPHUKHLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26N2O
Molecular Weight 250.38 g/mol
Exact Mass 250.204513457 g/mol
Topological Polar Surface Area (TPSA) 26.70 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.66
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4-Hydroxylupanine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9767 97.67%
Caco-2 + 0.5221 52.21%
Blood Brain Barrier + 0.9316 93.16%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6247 62.47%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.9413 94.13%
OATP1B3 inhibitior + 0.9495 94.95%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.7250 72.50%
BSEP inhibitior - 0.8033 80.33%
P-glycoprotein inhibitior - 0.9606 96.06%
P-glycoprotein substrate - 0.7910 79.10%
CYP3A4 substrate - 0.5769 57.69%
CYP2C9 substrate - 0.8190 81.90%
CYP2D6 substrate + 0.5575 55.75%
CYP3A4 inhibition - 0.9800 98.00%
CYP2C9 inhibition - 0.9631 96.31%
CYP2C19 inhibition - 0.9193 91.93%
CYP2D6 inhibition - 0.8240 82.40%
CYP1A2 inhibition - 0.8480 84.80%
CYP2C8 inhibition - 0.9514 95.14%
CYP inhibitory promiscuity - 0.9725 97.25%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6731 67.31%
Eye corrosion - 0.9206 92.06%
Eye irritation + 0.8508 85.08%
Skin irritation - 0.6262 62.62%
Skin corrosion - 0.7589 75.89%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5439 54.39%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.7814 78.14%
skin sensitisation - 0.8964 89.64%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.6479 64.79%
Acute Oral Toxicity (c) III 0.7400 74.00%
Estrogen receptor binding - 0.7794 77.94%
Androgen receptor binding - 0.5336 53.36%
Thyroid receptor binding - 0.5696 56.96%
Glucocorticoid receptor binding - 0.6317 63.17%
Aromatase binding - 0.8296 82.96%
PPAR gamma - 0.8750 87.50%
Honey bee toxicity - 0.9209 92.09%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity - 0.9555 95.55%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.85% 97.25%
CHEMBL3023 Q9NRA0 Sphingosine kinase 2 88.90% 95.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.67% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.68% 97.09%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 86.60% 95.50%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 86.57% 96.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.99% 95.89%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 85.90% 83.57%
CHEMBL1978 P11511 Cytochrome P450 19A1 85.64% 91.76%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 85.52% 95.58%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 83.13% 94.78%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.49% 93.04%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 82.22% 98.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.31% 93.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.59% 92.94%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 80.36% 98.46%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.33% 93.03%
CHEMBL4235 P28845 11-beta-hydroxysteroid dehydrogenase 1 80.11% 97.98%

Plants that contains it

Top
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.
Cytisus scoparius
Genista majorica
Lupinus arboreus
Lupinus latifolius
Lupinus luteus
Lupinus mexicanus
Lupinus mutabilis
Lupinus polyphyllus
Virgilia divaricata

Cross-Links

Top
PubChem 6427216
LOTUS LTS0244791
wikiData Q104253254