Isoptelefolidine

Details

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Internal ID f70eb993-dce0-40c4-8daf-c79604fd1fde
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives
IUPAC Name 1-(6,8-dimethoxy-[1,3]dioxolo[4,5-h]quinolin-7-yl)-3-methylbut-3-en-2-ol
SMILES (Canonical) CC(=C)C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O
SMILES (Isomeric) CC(=C)C(CC1=C(C2=C(C3=C(C=C2)OCO3)N=C1OC)OC)O
InChI InChI=1S/C17H19NO5/c1-9(2)12(19)7-11-15(20-3)10-5-6-13-16(23-8-22-13)14(10)18-17(11)21-4/h5-6,12,19H,1,7-8H2,2-4H3
InChI Key WSGNACAVADSXNC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H19NO5
Molecular Weight 317.34 g/mol
Exact Mass 317.12632271 g/mol
Topological Polar Surface Area (TPSA) 70.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.46
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Isoptelefolidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9680 96.80%
Caco-2 + 0.7645 76.45%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4132 41.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9101 91.01%
OATP1B3 inhibitior + 0.9319 93.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6344 63.44%
P-glycoprotein inhibitior - 0.8200 82.00%
P-glycoprotein substrate - 0.7473 74.73%
CYP3A4 substrate + 0.5520 55.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7040 70.40%
CYP3A4 inhibition + 0.8260 82.60%
CYP2C9 inhibition - 0.7377 73.77%
CYP2C19 inhibition - 0.6409 64.09%
CYP2D6 inhibition - 0.8597 85.97%
CYP1A2 inhibition + 0.6481 64.81%
CYP2C8 inhibition - 0.6377 63.77%
CYP inhibitory promiscuity + 0.6129 61.29%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5735 57.35%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.6046 60.46%
Skin irritation - 0.7870 78.70%
Skin corrosion - 0.9388 93.88%
Ames mutagenesis + 0.5846 58.46%
Human Ether-a-go-go-Related Gene inhibition - 0.5863 58.63%
Micronuclear + 0.6059 60.59%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.7917 79.17%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6337 63.37%
Acute Oral Toxicity (c) III 0.5771 57.71%
Estrogen receptor binding + 0.7410 74.10%
Androgen receptor binding - 0.5425 54.25%
Thyroid receptor binding + 0.7112 71.12%
Glucocorticoid receptor binding + 0.7581 75.81%
Aromatase binding - 0.4845 48.45%
PPAR gamma + 0.7027 70.27%
Honey bee toxicity - 0.8091 80.91%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.7849 78.49%

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 95.52% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.35% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.96% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.40% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.75% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.47% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.36% 96.77%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.31% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.12% 96.00%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 84.79% 80.96%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.42% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 83.66% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.82% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.28% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.09% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.09% 95.56%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.16% 92.68%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.05% 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.
Orixa japonica

Cross-Links

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PubChem 101663727
NPASS NPC72803
LOTUS LTS0014947
wikiData Q104398945