Buphanisine

Details

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Internal ID bc61b496-b352-472f-af2b-7695cc2618c5
Taxonomy Alkaloids and derivatives > Amaryllidaceae alkaloids > Crinine- and Haemanthamine-type amaryllidaceae alkaloids
IUPAC Name (1S,13R,15R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene
SMILES (Canonical) COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1
SMILES (Isomeric) CO[C@@H]1C[C@@H]2[C@@]3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1
InChI InChI=1S/C17H19NO3/c1-19-12-2-3-17-4-5-18(16(17)7-12)9-11-6-14-15(8-13(11)17)21-10-20-14/h2-3,6,8,12,16H,4-5,7,9-10H2,1H3/t12-,16+,17+/m0/s1
InChI Key HATSAIPBKRRCME-JCURWCKSSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C17H19NO3
Molecular Weight 285.34 g/mol
Exact Mass 285.13649347 g/mol
Topological Polar Surface Area (TPSA) 30.90 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.22
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Buphanisine
(-)-buphanisine
CHEMBL512945

2D Structure

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2D Structure of Buphanisine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.9449 94.49%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.4601 46.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9376 93.76%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.6606 66.06%
P-glycoprotein inhibitior - 0.8299 82.99%
P-glycoprotein substrate - 0.5671 56.71%
CYP3A4 substrate + 0.5985 59.85%
CYP2C9 substrate - 0.6221 62.21%
CYP2D6 substrate + 0.4829 48.29%
CYP3A4 inhibition - 0.5655 56.55%
CYP2C9 inhibition - 0.8977 89.77%
CYP2C19 inhibition - 0.5627 56.27%
CYP2D6 inhibition + 0.7412 74.12%
CYP1A2 inhibition - 0.5792 57.92%
CYP2C8 inhibition - 0.8349 83.49%
CYP inhibitory promiscuity - 0.5342 53.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5429 54.29%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9836 98.36%
Skin irritation - 0.7932 79.32%
Skin corrosion - 0.9384 93.84%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6813 68.13%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.6178 61.78%
skin sensitisation - 0.7989 79.89%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity + 0.7093 70.93%
Acute Oral Toxicity (c) III 0.5989 59.89%
Estrogen receptor binding + 0.5700 57.00%
Androgen receptor binding + 0.5761 57.61%
Thyroid receptor binding + 0.7004 70.04%
Glucocorticoid receptor binding + 0.5894 58.94%
Aromatase binding + 0.5346 53.46%
PPAR gamma - 0.5180 51.80%
Honey bee toxicity - 0.6582 65.82%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7124 71.24%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.64% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.94% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.96% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.63% 94.45%
CHEMBL240 Q12809 HERG 92.89% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.10% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.82% 97.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.96% 94.80%
CHEMBL4208 P20618 Proteasome component C5 86.07% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.91% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.27% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.21% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.08% 100.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 84.31% 82.67%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 84.00% 80.96%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 83.81% 90.95%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.75% 82.38%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.19% 89.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.66% 90.71%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.30% 90.24%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.20% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.96% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.60% 93.04%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.90% 94.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.71% 91.03%
CHEMBL233 P35372 Mu opioid receptor 80.55% 97.93%

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.
Ammocharis tinneana
Brunsvigia josephinae
Brunsvigia orientalis
Crinum asiaticum
Crossyne flava
Galanthus elwesii
Neorautanenia mitis
Nerine bowdenii

Cross-Links

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PubChem 12302149
NPASS NPC78733
LOTUS LTS0275387
wikiData Q104402423