(2S,3S,6R)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-9-one

Details

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Internal ID f2b4c6a9-1220-4fd7-b07b-7522458f736c
Taxonomy Alkaloids and derivatives > Cephalotaxus alkaloids
IUPAC Name (2S,3S,6R)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-9-one
SMILES (Canonical) COC1=CC23CCC(=O)N2CCC4=CC5=C(C=C4C3C1O)OCO5
SMILES (Isomeric) COC1=C[C@]23CCC(=O)N2CCC4=CC5=C(C=C4[C@@H]3[C@@H]1O)OCO5
InChI InChI=1S/C18H19NO5/c1-22-14-8-18-4-2-15(20)19(18)5-3-10-6-12-13(24-9-23-12)7-11(10)16(18)17(14)21/h6-8,16-17,21H,2-5,9H2,1H3/t16-,17-,18+/m1/s1
InChI Key WLFMEQAKLOQAMK-KURKYZTESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H19NO5
Molecular Weight 329.30 g/mol
Exact Mass 329.12632271 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.32
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3S,6R)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9627 96.27%
Caco-2 + 0.7573 75.73%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7325 73.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9335 93.35%
OATP1B3 inhibitior + 0.9483 94.83%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.7192 71.92%
P-glycoprotein substrate - 0.8342 83.42%
CYP3A4 substrate + 0.6399 63.99%
CYP2C9 substrate - 0.7861 78.61%
CYP2D6 substrate - 0.7852 78.52%
CYP3A4 inhibition + 0.6627 66.27%
CYP2C9 inhibition - 0.8420 84.20%
CYP2C19 inhibition - 0.6315 63.15%
CYP2D6 inhibition - 0.7439 74.39%
CYP1A2 inhibition - 0.7237 72.37%
CYP2C8 inhibition - 0.8726 87.26%
CYP inhibitory promiscuity - 0.7036 70.36%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4782 47.82%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.9608 96.08%
Skin irritation - 0.7740 77.40%
Skin corrosion - 0.9255 92.55%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5787 57.87%
Micronuclear + 0.6900 69.00%
Hepatotoxicity - 0.5447 54.47%
skin sensitisation - 0.8320 83.20%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.5792 57.92%
Acute Oral Toxicity (c) III 0.6058 60.58%
Estrogen receptor binding + 0.7760 77.60%
Androgen receptor binding + 0.6465 64.65%
Thyroid receptor binding + 0.6111 61.11%
Glucocorticoid receptor binding + 0.7616 76.16%
Aromatase binding + 0.5436 54.36%
PPAR gamma + 0.6605 66.05%
Honey bee toxicity - 0.8239 82.39%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7989 79.89%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.86% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.86% 96.77%
CHEMBL2581 P07339 Cathepsin D 95.69% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.47% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.81% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.54% 95.56%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 91.16% 82.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.25% 86.33%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.89% 93.40%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.43% 92.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.06% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.33% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.23% 89.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.94% 95.89%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 83.94% 90.24%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.70% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.52% 93.04%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.00% 93.99%
CHEMBL340 P08684 Cytochrome P450 3A4 82.08% 91.19%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 81.89% 97.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.49% 94.00%
CHEMBL4105786 P41182 B-cell lymphoma 6 protein 80.18% 92.86%

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.
Cephalotaxus fortunei
Cephalotaxus hainanensis
Taxus baccata

Cross-Links

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PubChem 11461634
NPASS NPC16647