Levallorphan

Details

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Internal ID af678ad4-c50b-40a8-a3df-9235c0dffd0c
Taxonomy Alkaloids and derivatives > Morphinans
IUPAC Name (1R,9R,10R)-17-prop-2-enyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-trien-4-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H25NO/c1-2-10-20-11-9-19-8-4-3-5-16(19)18(20)12-14-6-7-15(21)13-17(14)19/h2,6-7,13,16,18,21H,1,3-5,8-12H2/t16-,18+,19+/m0/s1
InChI Key OZYUPQUCAUTOBP-QXAKKESOSA-N
Popularity 1,088 references in papers

Physical and Chemical Properties

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Molecular Formula C19H25NO
Molecular Weight 283.40 g/mol
Exact Mass 283.193614421 g/mol
Topological Polar Surface Area (TPSA) 23.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.64
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Naloxiphan
152-02-3
Levallorphane
Levalorfano
17-Allylmorphinan-3-ol
Levallorphanum
Levallofano
N-Allyl-3-hydroxymorphinan
L-N-Allyl-3-hydroxymorphinan
(-)-3-Hydroxy-N-allylmorphinan
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Levallorphan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9857 98.57%
Caco-2 + 0.8703 87.03%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6132 61.32%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior - 0.3276 32.76%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior + 0.7500 75.00%
BSEP inhibitior - 0.6243 62.43%
P-glycoprotein inhibitior - 0.9078 90.78%
P-glycoprotein substrate + 0.6130 61.30%
CYP3A4 substrate + 0.5974 59.74%
CYP2C9 substrate - 0.5925 59.25%
CYP2D6 substrate + 0.7061 70.61%
CYP3A4 inhibition - 0.8409 84.09%
CYP2C9 inhibition - 0.8877 88.77%
CYP2C19 inhibition - 0.8743 87.43%
CYP2D6 inhibition + 0.8931 89.31%
CYP1A2 inhibition - 0.5676 56.76%
CYP2C8 inhibition + 0.4936 49.36%
CYP inhibitory promiscuity - 0.5908 59.08%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6343 63.43%
Eye corrosion - 0.9836 98.36%
Eye irritation - 0.9541 95.41%
Skin irritation - 0.6253 62.53%
Skin corrosion - 0.8297 82.97%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8698 86.98%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.9000 90.00%
skin sensitisation - 0.7713 77.13%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.9402 94.02%
Acute Oral Toxicity (c) III 0.7997 79.97%
Estrogen receptor binding - 0.7432 74.32%
Androgen receptor binding + 0.7998 79.98%
Thyroid receptor binding - 0.4910 49.10%
Glucocorticoid receptor binding - 0.6483 64.83%
Aromatase binding - 0.5817 58.17%
PPAR gamma + 0.5560 55.60%
Honey bee toxicity - 0.8018 80.18%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.7165 71.65%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL233 P35372 Mu opioid receptor 1.69 nM
0.48 nM
1.29 nM
Ki
Ki
Ki
PMID: 21621410
PMID: 21621410
PMID: 21621410

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL233 P35372 Mu opioid receptor 99.70% 97.93%
CHEMBL236 P41143 Delta opioid receptor 99.44% 99.35%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.24% 96.09%
CHEMBL237 P41145 Kappa opioid receptor 97.14% 98.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.39% 91.11%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 94.47% 83.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.16% 95.89%
CHEMBL2581 P07339 Cathepsin D 92.07% 98.95%
CHEMBL240 Q12809 HERG 91.10% 89.76%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.10% 89.62%
CHEMBL217 P14416 Dopamine D2 receptor 91.04% 95.62%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.60% 93.40%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.43% 93.99%
CHEMBL238 Q01959 Dopamine transporter 89.38% 95.88%
CHEMBL5203 P33316 dUTP pyrophosphatase 88.78% 99.18%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.49% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.99% 94.45%
CHEMBL242 Q92731 Estrogen receptor beta 86.16% 98.35%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.94% 93.04%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.38% 91.03%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.42% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.22% 100.00%
CHEMBL228 P31645 Serotonin transporter 83.43% 95.51%
CHEMBL4208 P20618 Proteasome component C5 82.06% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.99% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.75% 90.71%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.32% 94.78%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.20% 92.94%

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.
Papaver somniferum

Cross-Links

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PubChem 5359371
NPASS NPC124802
ChEMBL CHEMBL1254682
LOTUS LTS0020080
wikiData Q6534827