N-Ethoxycarbonylethylcrinasiadine

Details

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Internal ID 211f8bd2-0e71-455d-b090-f7b07a6eac0b
Taxonomy Alkaloids and derivatives > Amaryllidaceae alkaloids > Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
IUPAC Name ethyl 3-(6-oxo-[1,3]dioxolo[4,5-j]phenanthridin-5-yl)propanoate
SMILES (Canonical) CCOC(=O)CCN1C2=CC=CC=C2C3=CC4=C(C=C3C1=O)OCO4
SMILES (Isomeric) CCOC(=O)CCN1C2=CC=CC=C2C3=CC4=C(C=C3C1=O)OCO4
InChI InChI=1S/C19H17NO5/c1-2-23-18(21)7-8-20-15-6-4-3-5-12(15)13-9-16-17(25-11-24-16)10-14(13)19(20)22/h3-6,9-10H,2,7-8,11H2,1H3
InChI Key NITMZBGVDDZNHZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H17NO5
Molecular Weight 339.30 g/mol
Exact Mass 339.11067264 g/mol
Topological Polar Surface Area (TPSA) 65.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.84
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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CHEMBL2208206

2D Structure

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2D Structure of N-Ethoxycarbonylethylcrinasiadine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9643 96.43%
Caco-2 + 0.7496 74.96%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7065 70.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9223 92.23%
OATP1B3 inhibitior + 0.9324 93.24%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.6327 63.27%
P-glycoprotein inhibitior + 0.6850 68.50%
P-glycoprotein substrate - 0.8778 87.78%
CYP3A4 substrate + 0.6144 61.44%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.8778 87.78%
CYP3A4 inhibition + 0.8582 85.82%
CYP2C9 inhibition + 0.7498 74.98%
CYP2C19 inhibition + 0.9598 95.98%
CYP2D6 inhibition - 0.8618 86.18%
CYP1A2 inhibition + 0.7435 74.35%
CYP2C8 inhibition - 0.7220 72.20%
CYP inhibitory promiscuity + 0.9394 93.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5211 52.11%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.8999 89.99%
Skin irritation - 0.8467 84.67%
Skin corrosion - 0.9475 94.75%
Ames mutagenesis + 0.5246 52.46%
Human Ether-a-go-go-Related Gene inhibition - 0.5800 58.00%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.7336 73.36%
skin sensitisation - 0.8855 88.55%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7954 79.54%
Acute Oral Toxicity (c) III 0.7468 74.68%
Estrogen receptor binding + 0.7794 77.94%
Androgen receptor binding + 0.5741 57.41%
Thyroid receptor binding + 0.6546 65.46%
Glucocorticoid receptor binding + 0.7272 72.72%
Aromatase binding + 0.6985 69.85%
PPAR gamma + 0.6064 60.64%
Honey bee toxicity - 0.9019 90.19%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9007 90.07%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.66% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.60% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.31% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.17% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.34% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.01% 92.62%
CHEMBL2581 P07339 Cathepsin D 90.50% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.06% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.22% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.54% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.47% 99.17%
CHEMBL255 P29275 Adenosine A2b receptor 83.58% 98.59%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.38% 96.00%
CHEMBL4208 P20618 Proteasome component C5 81.00% 90.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.06% 94.80%

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.
Zephyranthes candida

Cross-Links

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PubChem 71454344
LOTUS LTS0089917
wikiData Q105179994