Claulansine F

Details

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Internal ID 5c4f95d8-0170-4e78-846c-e5f3ca171447
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 8-methoxy-3,3-dimethyl-11H-pyrano[3,2-a]carbazole-5-carbaldehyde
SMILES (Canonical) CC1(C=CC2=C(O1)C(=CC3=C2NC4=C3C=C(C=C4)OC)C=O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C(=CC3=C2NC4=C3C=C(C=C4)OC)C=O)C
InChI InChI=1S/C19H17NO3/c1-19(2)7-6-13-17-15(8-11(10-21)18(13)23-19)14-9-12(22-3)4-5-16(14)20-17/h4-10,20H,1-3H3
InChI Key QBWFLAHUWCLAKK-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C19H17NO3
Molecular Weight 307.30 g/mol
Exact Mass 307.12084340 g/mol
Topological Polar Surface Area (TPSA) 51.30 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.33
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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CHEMBL2035835

2D Structure

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2D Structure of Claulansine F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7680 76.80%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7111 71.11%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.7999 79.99%
OATP1B3 inhibitior + 0.9656 96.56%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8787 87.87%
P-glycoprotein inhibitior + 0.5935 59.35%
P-glycoprotein substrate - 0.5828 58.28%
CYP3A4 substrate + 0.6090 60.90%
CYP2C9 substrate + 0.5870 58.70%
CYP2D6 substrate - 0.7769 77.69%
CYP3A4 inhibition + 0.6262 62.62%
CYP2C9 inhibition - 0.5906 59.06%
CYP2C19 inhibition + 0.7720 77.20%
CYP2D6 inhibition - 0.7108 71.08%
CYP1A2 inhibition + 0.8973 89.73%
CYP2C8 inhibition + 0.4615 46.15%
CYP inhibitory promiscuity + 0.8537 85.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.5825 58.25%
Eye corrosion - 0.9886 98.86%
Eye irritation + 0.7523 75.23%
Skin irritation - 0.8469 84.69%
Skin corrosion - 0.9617 96.17%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6049 60.49%
Micronuclear + 0.6500 65.00%
Hepatotoxicity - 0.6061 60.61%
skin sensitisation - 0.8228 82.28%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6035 60.35%
Acute Oral Toxicity (c) III 0.5185 51.85%
Estrogen receptor binding + 0.9641 96.41%
Androgen receptor binding + 0.6848 68.48%
Thyroid receptor binding + 0.8769 87.69%
Glucocorticoid receptor binding + 0.9510 95.10%
Aromatase binding + 0.9082 90.82%
PPAR gamma + 0.7412 74.12%
Honey bee toxicity - 0.8081 80.81%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.8019 80.19%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.25% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.88% 91.11%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 96.00% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.78% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.97% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 94.96% 91.49%
CHEMBL4208 P20618 Proteasome component C5 92.66% 90.00%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 91.44% 93.24%
CHEMBL1907 P15144 Aminopeptidase N 90.91% 93.31%
CHEMBL255 P29275 Adenosine A2b receptor 88.34% 98.59%
CHEMBL2535 P11166 Glucose transporter 86.00% 98.75%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 85.99% 85.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.40% 94.00%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 84.46% 89.44%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.74% 91.71%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 82.07% 80.96%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.84% 100.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.61% 94.80%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.54% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.34% 86.92%
CHEMBL2581 P07339 Cathepsin D 81.33% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.78% 89.00%

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.
Clausena lansium

Cross-Links

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PubChem 57409550
NPASS NPC35223