13-Hydroxymultiflorine

Details

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Internal ID cd6bc180-7f94-4221-afeb-19c1c527f4de
Taxonomy Alkaloids and derivatives > Lupin alkaloids > Sparteine, lupanine, and related alkaloids
IUPAC Name 12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-one
SMILES (Canonical) C1CN2CC3CC(C2CC1O)CN4C3CC(=O)CC4
SMILES (Isomeric) C1CN2CC3CC(C2CC1O)CN4C3CC(=O)CC4
InChI InChI=1S/C15H24N2O2/c18-12-1-3-16-8-10-5-11(14(16)6-12)9-17-4-2-13(19)7-15(10)17/h10-12,14-15,18H,1-9H2
InChI Key XSWCLXUQXOJCGT-UHFFFAOYSA-N
Popularity 2 references 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 0.20
Atomic LogP (AlogP) 0.49
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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XSWCLXUQXOJCGT-UHFFFAOYSA-N

2D Structure

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2D Structure of 13-Hydroxymultiflorine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.5945 59.45%
Blood Brain Barrier + 0.8944 89.44%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7899 78.99%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9634 96.34%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.6365 63.65%
P-glycoprotein inhibitior - 0.9068 90.68%
P-glycoprotein substrate - 0.7151 71.51%
CYP3A4 substrate - 0.5298 52.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5516 55.16%
CYP3A4 inhibition - 0.9219 92.19%
CYP2C9 inhibition - 0.9321 93.21%
CYP2C19 inhibition - 0.9393 93.93%
CYP2D6 inhibition - 0.8306 83.06%
CYP1A2 inhibition - 0.8783 87.83%
CYP2C8 inhibition - 0.9764 97.64%
CYP inhibitory promiscuity - 0.9816 98.16%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9630 96.30%
Carcinogenicity (trinary) Non-required 0.6356 63.56%
Eye corrosion - 0.9370 93.70%
Eye irritation - 0.5487 54.87%
Skin irritation - 0.6161 61.61%
Skin corrosion - 0.8211 82.11%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6220 62.20%
Micronuclear + 0.5900 59.00%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation - 0.8747 87.47%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5973 59.73%
Acute Oral Toxicity (c) III 0.6812 68.12%
Estrogen receptor binding - 0.6857 68.57%
Androgen receptor binding - 0.5883 58.83%
Thyroid receptor binding - 0.6811 68.11%
Glucocorticoid receptor binding - 0.5628 56.28%
Aromatase binding - 0.6820 68.20%
PPAR gamma - 0.7987 79.87%
Honey bee toxicity - 0.8339 83.39%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.9687 96.87%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.73% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.45% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.44% 97.09%
CHEMBL217 P14416 Dopamine D2 receptor 85.34% 95.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.93% 95.89%
CHEMBL2581 P07339 Cathepsin D 84.66% 98.95%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.15% 93.03%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.04% 96.09%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 83.69% 96.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.34% 97.25%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 83.04% 98.46%
CHEMBL3023 Q9NRA0 Sphingosine kinase 2 81.33% 95.61%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.72% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.32% 99.23%

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.
Lupinus albus
Lupinus linearis

Cross-Links

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PubChem 85280874
LOTUS LTS0066467
wikiData Q104250365