(14R,24S)-24-methoxy-13-methyl-5,7,19,21,25-pentaoxa-13-azahexacyclo[12.11.0.02,10.04,8.015,23.018,22]pentacosa-2,4(8),9,15(23),16,18(22)-hexaene

Details

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Internal ID 1f83a804-2368-4c1a-b04e-c9533a783f15
Taxonomy Alkaloids and derivatives > Rhoeadine alkaloids
IUPAC Name (14R,24S)-24-methoxy-13-methyl-5,7,19,21,25-pentaoxa-13-azahexacyclo[12.11.0.02,10.04,8.015,23.018,22]pentacosa-2,4(8),9,15(23),16,18(22)-hexaene
SMILES (Canonical) CN1CCC2=CC3=C(C=C2C4C1C5=C(C(O4)OC)C6=C(C=C5)OCO6)OCO3
SMILES (Isomeric) CN1CCC2=CC3=C(C=C2C4[C@H]1C5=C([C@H](O4)OC)C6=C(C=C5)OCO6)OCO3
InChI InChI=1S/C21H21NO6/c1-22-6-5-11-7-15-16(26-9-25-15)8-13(11)19-18(22)12-3-4-14-20(27-10-24-14)17(12)21(23-2)28-19/h3-4,7-8,18-19,21H,5-6,9-10H2,1-2H3/t18-,19?,21+/m1/s1
InChI Key XRBIHOLQAKITPP-DRPMKMPGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H21NO6
Molecular Weight 383.40 g/mol
Exact Mass 383.13688739 g/mol
Topological Polar Surface Area (TPSA) 58.60 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.09
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (14R,24S)-24-methoxy-13-methyl-5,7,19,21,25-pentaoxa-13-azahexacyclo[12.11.0.02,10.04,8.015,23.018,22]pentacosa-2,4(8),9,15(23),16,18(22)-hexaene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9297 92.97%
Caco-2 + 0.8677 86.77%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.6346 63.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9221 92.21%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9022 90.22%
P-glycoprotein inhibitior + 0.6672 66.72%
P-glycoprotein substrate - 0.6543 65.43%
CYP3A4 substrate + 0.6245 62.45%
CYP2C9 substrate + 0.5774 57.74%
CYP2D6 substrate + 0.7008 70.08%
CYP3A4 inhibition - 0.5804 58.04%
CYP2C9 inhibition - 0.6193 61.93%
CYP2C19 inhibition + 0.5465 54.65%
CYP2D6 inhibition + 0.5566 55.66%
CYP1A2 inhibition - 0.5077 50.77%
CYP2C8 inhibition - 0.7763 77.63%
CYP inhibitory promiscuity - 0.5201 52.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5998 59.98%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.9793 97.93%
Skin irritation - 0.7835 78.35%
Skin corrosion - 0.9394 93.94%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7265 72.65%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.8493 84.93%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6823 68.23%
Acute Oral Toxicity (c) III 0.7122 71.22%
Estrogen receptor binding + 0.7210 72.10%
Androgen receptor binding + 0.7203 72.03%
Thyroid receptor binding + 0.5455 54.55%
Glucocorticoid receptor binding + 0.8689 86.89%
Aromatase binding - 0.5682 56.82%
PPAR gamma + 0.7570 75.70%
Honey bee toxicity - 0.8279 82.79%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.3631 36.31%

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
CHEMBL5697 Q9GZT9 Egl nine homolog 1 97.74% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.51% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.99% 96.77%
CHEMBL2581 P07339 Cathepsin D 93.60% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.86% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.45% 86.33%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 89.53% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.24% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.98% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.66% 95.89%
CHEMBL2056 P21728 Dopamine D1 receptor 87.61% 91.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.17% 92.62%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 85.00% 90.95%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 84.79% 82.67%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.08% 95.89%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 83.80% 96.39%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.27% 93.99%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 81.54% 96.42%
CHEMBL3401 O75469 Pregnane X receptor 81.47% 94.73%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.40% 100.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.87% 89.62%

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 rhoeas
Papaver somniferum
Taxus baccata

Cross-Links

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PubChem 5318652
NPASS NPC247684