Nuttalline

Details

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Internal ID dc7fb809-cd17-487a-be81-d676b22f0ba1
Taxonomy Alkaloids and derivatives > Lupin alkaloids > Sparteine, lupanine, and related alkaloids
IUPAC Name 4-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one
SMILES (Canonical) C1CCN2CC3CC(C2C1)CN4C3CC(CC4=O)O
SMILES (Isomeric) C1CCN2CC3CC(C2C1)CN4C3CC(CC4=O)O
InChI InChI=1S/C15H24N2O2/c18-12-6-14-10-5-11(9-17(14)15(19)7-12)13-3-1-2-4-16(13)8-10/h10-14,18H,1-9H2
InChI Key GIQKWLHFWBBSSV-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24N2O2
Molecular Weight 264.36 g/mol
Exact Mass 264.183778013 g/mol
Topological Polar Surface Area (TPSA) 43.80 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.84
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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23360-87-4
Nuttaline
4-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one
4beta-Hydroxylupanine
4-Hydroxyspartein-2-one #
GIQKWLHFWBBSSV-UHFFFAOYSA-N
7,14-Methano-4H,6H-dipyrido[1,2-a:1',2'-e][1,5]diazocin-4-one, dodecahydro-2-hydroxy-, [2S-(2.alpha.,7.alpha.,7a.beta.,14.alpha.,14a.alpha.)]-
7,14-Methano-4H,6H-dipyrido(1,2-a:1',2'-e)(1,5)diazocin-4-one, dodecahydro-2-hydroxy-, (2S-(2alpha,7alpha,7abeta,14alpha,14aalpha))-

2D Structure

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2D Structure of Nuttalline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.6633 66.33%
Blood Brain Barrier + 0.8879 88.79%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7215 72.15%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9364 93.64%
OATP1B3 inhibitior + 0.9519 95.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.7225 72.25%
P-glycoprotein inhibitior - 0.9252 92.52%
P-glycoprotein substrate - 0.6846 68.46%
CYP3A4 substrate - 0.5451 54.51%
CYP2C9 substrate - 0.8121 81.21%
CYP2D6 substrate + 0.4247 42.47%
CYP3A4 inhibition - 0.9453 94.53%
CYP2C9 inhibition - 0.9415 94.15%
CYP2C19 inhibition - 0.8527 85.27%
CYP2D6 inhibition - 0.8784 87.84%
CYP1A2 inhibition - 0.8442 84.42%
CYP2C8 inhibition - 0.9733 97.33%
CYP inhibitory promiscuity - 0.9505 95.05%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5873 58.73%
Eye corrosion - 0.9692 96.92%
Eye irritation - 0.6664 66.64%
Skin irritation - 0.7488 74.88%
Skin corrosion - 0.9059 90.59%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6092 60.92%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.6380 63.80%
skin sensitisation - 0.8921 89.21%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.7526 75.26%
Acute Oral Toxicity (c) III 0.6746 67.46%
Estrogen receptor binding - 0.4934 49.34%
Androgen receptor binding - 0.4854 48.54%
Thyroid receptor binding - 0.5649 56.49%
Glucocorticoid receptor binding - 0.6030 60.30%
Aromatase binding - 0.6896 68.96%
PPAR gamma - 0.7085 70.85%
Honey bee toxicity - 0.9117 91.17%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity - 0.9791 97.91%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.38% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.66% 97.09%
CHEMBL2581 P07339 Cathepsin D 88.91% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.20% 95.89%
CHEMBL1978 P11511 Cytochrome P450 19A1 87.74% 91.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.47% 96.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.51% 93.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.39% 95.56%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 86.30% 95.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.94% 93.04%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.71% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.87% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.56% 90.71%
CHEMBL3922 P50579 Methionine aminopeptidase 2 84.20% 97.28%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 82.58% 96.03%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 82.35% 94.78%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.73% 98.33%
CHEMBL3012 Q13946 Phosphodiesterase 7A 81.28% 99.29%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.98% 93.00%
CHEMBL237 P41145 Kappa opioid receptor 80.89% 98.10%
CHEMBL3023 Q9NRA0 Sphingosine kinase 2 80.69% 95.61%

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.
Lebeckia plukenetiana
Pinus hartwegii

Cross-Links

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PubChem 161417
LOTUS LTS0087503
wikiData Q105009146