Clausenawalline I

Details

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Internal ID 5d000329-8bae-42a5-9b9e-66aae384430b
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carbaldehyde
SMILES (Canonical) CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=CC(=C4)C=O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=CC(=C4)C=O)C
InChI InChI=1S/C18H15NO2/c1-18(2)8-7-12-16(21-18)6-5-15-17(12)13-9-11(10-20)3-4-14(13)19-15/h3-10,19H,1-2H3
InChI Key CRDPWFBUQAXUOR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H15NO2
Molecular Weight 277.30 g/mol
Exact Mass 277.110278721 g/mol
Topological Polar Surface Area (TPSA) 42.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.32
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Clausenawalline I

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 + 0.7394 73.94%
Blood Brain Barrier + 0.6879 68.79%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7319 73.19%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.8230 82.30%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9047 90.47%
P-glycoprotein inhibitior - 0.5486 54.86%
P-glycoprotein substrate - 0.7872 78.72%
CYP3A4 substrate + 0.5513 55.13%
CYP2C9 substrate + 0.6037 60.37%
CYP2D6 substrate - 0.7558 75.58%
CYP3A4 inhibition + 0.5818 58.18%
CYP2C9 inhibition + 0.6363 63.63%
CYP2C19 inhibition + 0.7329 73.29%
CYP2D6 inhibition - 0.6223 62.23%
CYP1A2 inhibition + 0.8672 86.72%
CYP2C8 inhibition - 0.6703 67.03%
CYP inhibitory promiscuity + 0.8721 87.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5441 54.41%
Eye corrosion - 0.9921 99.21%
Eye irritation + 0.5372 53.72%
Skin irritation - 0.7002 70.02%
Skin corrosion - 0.9564 95.64%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3712 37.12%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.5689 56.89%
skin sensitisation - 0.6698 66.98%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5205 52.05%
Acute Oral Toxicity (c) III 0.7342 73.42%
Estrogen receptor binding + 0.9730 97.30%
Androgen receptor binding + 0.7837 78.37%
Thyroid receptor binding + 0.8323 83.23%
Glucocorticoid receptor binding + 0.9007 90.07%
Aromatase binding + 0.8349 83.49%
PPAR gamma + 0.7075 70.75%
Honey bee toxicity - 0.8501 85.01%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8207 82.07%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.49% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.11% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.90% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.83% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.65% 89.00%
CHEMBL2581 P07339 Cathepsin D 89.52% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.41% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.01% 96.09%
CHEMBL255 P29275 Adenosine A2b receptor 87.00% 98.59%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.99% 85.30%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 84.69% 80.96%
CHEMBL3401 O75469 Pregnane X receptor 83.96% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.20% 86.33%
CHEMBL4208 P20618 Proteasome component C5 81.86% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.78% 100.00%

Cross-Links

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PubChem 71623858
NPASS NPC300991