(4aS,10bR)-Noroxomaritidine

Details

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Internal ID 32df9a5d-c546-4845-995a-5a52d7072b3e
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Phenanthridines and derivatives
IUPAC Name (1R,10S)-5-hydroxy-4-methoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraen-12-one
SMILES (Canonical) COC1=C(C=C2CN3CCC4(C3CC(=O)C=C4)C2=C1)O
SMILES (Isomeric) COC1=C(C=C2CN3CC[C@]4([C@@H]3CC(=O)C=C4)C2=C1)O
InChI InChI=1S/C16H17NO3/c1-20-14-8-12-10(6-13(14)19)9-17-5-4-16(12)3-2-11(18)7-15(16)17/h2-3,6,8,15,19H,4-5,7,9H2,1H3/t15-,16-/m0/s1
InChI Key VEXDOCFQMVMPHJ-HOTGVXAUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H17NO3
Molecular Weight 271.31 g/mol
Exact Mass 271.12084340 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.76
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL3899581
CHEBI:136557
C21405
(4aS,10bR)-8-hydroxy-9-methoxy-4,4a-dihydro-3H,6H-5,10b-ethanophenanthridin-3-one
(1R,10S)-5-hydroxy-4-methoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraen-12-one

2D Structure

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2D Structure of (4aS,10bR)-Noroxomaritidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.8063 80.63%
Blood Brain Barrier + 0.8317 83.17%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8314 83.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9261 92.61%
OATP1B3 inhibitior + 0.9525 95.25%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.6750 67.50%
BSEP inhibitior + 0.6113 61.13%
P-glycoprotein inhibitior - 0.9175 91.75%
P-glycoprotein substrate + 0.5440 54.40%
CYP3A4 substrate + 0.6370 63.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3919 39.19%
CYP3A4 inhibition - 0.5662 56.62%
CYP2C9 inhibition - 0.8422 84.22%
CYP2C19 inhibition - 0.7294 72.94%
CYP2D6 inhibition + 0.6465 64.65%
CYP1A2 inhibition - 0.7603 76.03%
CYP2C8 inhibition - 0.8578 85.78%
CYP inhibitory promiscuity - 0.7575 75.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5369 53.69%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9088 90.88%
Skin irritation - 0.7666 76.66%
Skin corrosion - 0.9389 93.89%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6128 61.28%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.5826 58.26%
skin sensitisation - 0.8442 84.42%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 1.0000 100.00%
Nephrotoxicity + 0.6218 62.18%
Acute Oral Toxicity (c) III 0.6039 60.39%
Estrogen receptor binding - 0.6316 63.16%
Androgen receptor binding - 0.5540 55.40%
Thyroid receptor binding - 0.5432 54.32%
Glucocorticoid receptor binding + 0.6485 64.85%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.6000 60.00%
Honey bee toxicity - 0.8297 82.97%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity - 0.3955 39.55%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.50% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.78% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.54% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.61% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 93.58% 90.71%
CHEMBL4208 P20618 Proteasome component C5 93.03% 90.00%
CHEMBL2581 P07339 Cathepsin D 91.91% 98.95%
CHEMBL217 P14416 Dopamine D2 receptor 91.77% 95.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.45% 86.33%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 91.13% 91.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.82% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.74% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.55% 94.00%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 87.35% 96.86%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.58% 93.40%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.03% 82.69%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 85.09% 91.79%
CHEMBL5747 Q92793 CREB-binding protein 84.83% 95.12%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.60% 89.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.40% 82.38%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.70% 93.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.33% 99.23%
CHEMBL2535 P11166 Glucose transporter 81.10% 98.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.42% 100.00%

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.
Atriplex muricata
Chromolaena laevigata
Crinum asiaticum
Crotalaria crispata
Haplopappus deserticola
Hesperocyparis arizonica
Seriphidium junceum
Viburnum lantana

Cross-Links

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PubChem 11184826
NPASS NPC290181
LOTUS LTS0084802
wikiData Q105284901