[(1S,13R,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate

Details

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Internal ID 21d6f036-42e3-4aa4-a824-c333982f1645
Taxonomy Alkaloids and derivatives > Amaryllidaceae alkaloids > Crinine- and Haemanthamine-type amaryllidaceae alkaloids
IUPAC Name [(1S,13R,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate
SMILES (Canonical) CC(=O)OC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1
SMILES (Isomeric) CC(=O)O[C@@H]1C[C@@H]2[C@@]3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1
InChI InChI=1S/C18H19NO4/c1-11(20)23-13-2-3-18-4-5-19(17(18)7-13)9-12-6-15-16(8-14(12)18)22-10-21-15/h2-3,6,8,13,17H,4-5,7,9-10H2,1H3/t13-,17+,18+/m0/s1
InChI Key YEIGSYFTXGPBIB-MORSLUCNSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C18H19NO4
Molecular Weight 313.30 g/mol
Exact Mass 313.13140809 g/mol
Topological Polar Surface Area (TPSA) 48.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.13
H-Bond Acceptor 5
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 [(1S,13R,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9840 98.40%
Caco-2 + 0.8168 81.68%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5315 53.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9282 92.82%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.6451 64.51%
P-glycoprotein inhibitior - 0.6778 67.78%
P-glycoprotein substrate - 0.6320 63.20%
CYP3A4 substrate + 0.6284 62.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition + 0.8240 82.40%
CYP2C9 inhibition - 0.8845 88.45%
CYP2C19 inhibition - 0.5095 50.95%
CYP2D6 inhibition + 0.6049 60.49%
CYP1A2 inhibition - 0.5467 54.67%
CYP2C8 inhibition - 0.8343 83.43%
CYP inhibitory promiscuity + 0.6089 60.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4854 48.54%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.9738 97.38%
Skin irritation - 0.8101 81.01%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4217 42.17%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.6303 63.03%
skin sensitisation - 0.7894 78.94%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.7063 70.63%
Acute Oral Toxicity (c) III 0.6600 66.00%
Estrogen receptor binding + 0.7378 73.78%
Androgen receptor binding + 0.5965 59.65%
Thyroid receptor binding + 0.7283 72.83%
Glucocorticoid receptor binding + 0.7205 72.05%
Aromatase binding - 0.5072 50.72%
PPAR gamma + 0.6255 62.55%
Honey bee toxicity - 0.7149 71.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5955 59.55%
Fish aquatic toxicity + 0.8376 83.76%

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 98.45% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.17% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.82% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.68% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.74% 86.33%
CHEMBL4208 P20618 Proteasome component C5 89.08% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.45% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.95% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.02% 94.80%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.39% 93.04%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.27% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 84.71% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.47% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.93% 97.25%
CHEMBL2581 P07339 Cathepsin D 83.84% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.09% 97.09%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 82.13% 90.95%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.87% 89.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.36% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.19% 92.62%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.08% 90.24%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.89% 99.23%
CHEMBL5028 O14672 ADAM10 80.40% 97.50%

Plants that contains it

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Cross-Links

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PubChem 101935954
NPASS NPC310782
LOTUS LTS0180812
wikiData Q105347259