Sphecoline F

Details

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Internal ID 0d0f28bf-4656-4f2b-b84b-3b34ec5622fd
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Pyridoindolones
IUPAC Name 1-acetyl-6-methoxy-2,9-dihydropyrido[3,4-b]indol-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H12N2O3/c1-7(17)13-14-10(6-12(18)16-13)9-5-8(19-2)3-4-11(9)15-14/h3-6,15H,1-2H3,(H,16,18)
InChI Key CZTGDZQYXKUNOD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H12N2O3
Molecular Weight 256.26 g/mol
Exact Mass 256.08479225 g/mol
Topological Polar Surface Area (TPSA) 67.40 Ų
XlogP 0.60
Atomic LogP (AlogP) 2.22
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Sphecoline F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 - 0.5973 59.73%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8441 84.41%
OATP2B1 inhibitior - 0.8630 86.30%
OATP1B1 inhibitior + 0.9289 92.89%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5844 58.44%
P-glycoprotein inhibitior - 0.8710 87.10%
P-glycoprotein substrate - 0.7710 77.10%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate + 0.6171 61.71%
CYP2D6 substrate - 0.8639 86.39%
CYP3A4 inhibition - 0.6456 64.56%
CYP2C9 inhibition - 0.7875 78.75%
CYP2C19 inhibition - 0.7846 78.46%
CYP2D6 inhibition - 0.9016 90.16%
CYP1A2 inhibition + 0.6807 68.07%
CYP2C8 inhibition - 0.7803 78.03%
CYP inhibitory promiscuity - 0.6642 66.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9423 94.23%
Carcinogenicity (trinary) Non-required 0.5971 59.71%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.8381 83.81%
Skin irritation - 0.8823 88.23%
Skin corrosion - 0.9711 97.11%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6637 66.37%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.6060 60.60%
skin sensitisation - 0.9471 94.71%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4743 47.43%
Acute Oral Toxicity (c) III 0.7240 72.40%
Estrogen receptor binding + 0.7803 78.03%
Androgen receptor binding + 0.7712 77.12%
Thyroid receptor binding + 0.5327 53.27%
Glucocorticoid receptor binding + 0.7271 72.71%
Aromatase binding + 0.7192 71.92%
PPAR gamma + 0.6648 66.48%
Honey bee toxicity - 0.9194 91.94%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.6010 60.10%

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 98.78% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.99% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.20% 96.09%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 93.07% 93.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.14% 95.56%
CHEMBL255 P29275 Adenosine A2b receptor 90.81% 98.59%
CHEMBL2581 P07339 Cathepsin D 90.59% 98.95%
CHEMBL4208 P20618 Proteasome component C5 89.25% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.47% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.97% 94.00%
CHEMBL2535 P11166 Glucose transporter 87.43% 98.75%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.43% 85.30%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.98% 99.17%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.81% 94.80%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.20% 86.92%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.32% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 81.23% 91.49%
CHEMBL4040 P28482 MAP kinase ERK2 80.34% 83.82%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.05% 92.94%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 146683997
LOTUS LTS0236947
wikiData Q104973143