Clausine I

Details

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Internal ID e6671102-67b7-4e72-92c5-83473ce1d9ea
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 1-hydroxy-6-methoxy-9H-carbazole-3-carbaldehyde
SMILES (Canonical) COC1=CC2=C(C=C1)NC3=C2C=C(C=C3O)C=O
SMILES (Isomeric) COC1=CC2=C(C=C1)NC3=C2C=C(C=C3O)C=O
InChI InChI=1S/C14H11NO3/c1-18-9-2-3-12-10(6-9)11-4-8(7-16)5-13(17)14(11)15-12/h2-7,15,17H,1H3
InChI Key AMRVXYRVPBLMCN-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C14H11NO3
Molecular Weight 241.24 g/mol
Exact Mass 241.07389321 g/mol
Topological Polar Surface Area (TPSA) 62.30 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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182261-94-5
1-hydroxy-6-methoxy-9H-carbazole-3-carbaldehyde
CHEMBL2036046
AKOS040735518

2D Structure

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2D Structure of Clausine 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 + 0.6776 67.76%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6734 67.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8435 84.35%
OATP1B3 inhibitior + 0.9629 96.29%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6208 62.08%
P-glycoprotein inhibitior - 0.8035 80.35%
P-glycoprotein substrate - 0.8388 83.88%
CYP3A4 substrate - 0.5072 50.72%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.7121 71.21%
CYP3A4 inhibition - 0.7389 73.89%
CYP2C9 inhibition - 0.5918 59.18%
CYP2C19 inhibition - 0.8503 85.03%
CYP2D6 inhibition - 0.9350 93.50%
CYP1A2 inhibition + 0.8073 80.73%
CYP2C8 inhibition - 0.6546 65.46%
CYP inhibitory promiscuity + 0.5223 52.23%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8833 88.33%
Carcinogenicity (trinary) Non-required 0.5020 50.20%
Eye corrosion - 0.9945 99.45%
Eye irritation + 0.8557 85.57%
Skin irritation - 0.8554 85.54%
Skin corrosion - 0.9766 97.66%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7569 75.69%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9357 93.57%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7010 70.10%
Acute Oral Toxicity (c) III 0.6002 60.02%
Estrogen receptor binding + 0.9143 91.43%
Androgen receptor binding + 0.6097 60.97%
Thyroid receptor binding + 0.6702 67.02%
Glucocorticoid receptor binding + 0.9491 94.91%
Aromatase binding + 0.8341 83.41%
PPAR gamma + 0.8057 80.57%
Honey bee toxicity - 0.9264 92.64%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.5100 51.00%

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 98.96% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.82% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.50% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.86% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.69% 96.09%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 90.39% 98.11%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 89.67% 93.24%
CHEMBL4208 P20618 Proteasome component C5 87.54% 90.00%
CHEMBL2535 P11166 Glucose transporter 87.48% 98.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 87.48% 91.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.24% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.07% 99.15%
CHEMBL1937 Q92769 Histone deacetylase 2 86.62% 94.75%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.06% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.87% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.73% 86.92%
CHEMBL2581 P07339 Cathepsin D 81.94% 98.95%

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 excavata
Clausena lansium

Cross-Links

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PubChem 10657725
NPASS NPC13327
LOTUS LTS0239611
wikiData Q104914901