Clausamine C

Details

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Internal ID 50552079-e635-422d-a38c-451e5252964e
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 2-(2-hydroxypropan-2-yl)-6-methoxy-2,7-dihydro-1H-pyrano[3,4-c]carbazol-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H19NO4/c1-19(2,22)15-9-11-12(18(21)24-15)8-14(23-3)17-16(11)10-6-4-5-7-13(10)20-17/h4-8,15,20,22H,9H2,1-3H3
InChI Key UWUXJRWRYLZZIF-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C19H19NO4
Molecular Weight 325.40 g/mol
Exact Mass 325.13140809 g/mol
Topological Polar Surface Area (TPSA) 71.60 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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CHEMBL517226
2-(2-hydroxypropan-2-yl)-6-methoxy-2,7-dihydro-1H-pyrano[3,4-c]carbazol-4-one

2D Structure

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2D Structure of Clausamine C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9662 96.62%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5421 54.21%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.8994 89.94%
OATP1B3 inhibitior + 0.9115 91.15%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8201 82.01%
P-glycoprotein inhibitior - 0.5693 56.93%
P-glycoprotein substrate - 0.6432 64.32%
CYP3A4 substrate + 0.6619 66.19%
CYP2C9 substrate - 0.8087 80.87%
CYP2D6 substrate - 0.8207 82.07%
CYP3A4 inhibition - 0.9124 91.24%
CYP2C9 inhibition - 0.8378 83.78%
CYP2C19 inhibition - 0.7709 77.09%
CYP2D6 inhibition - 0.7961 79.61%
CYP1A2 inhibition + 0.5335 53.35%
CYP2C8 inhibition + 0.4836 48.36%
CYP inhibitory promiscuity - 0.5313 53.13%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5071 50.71%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.7320 73.20%
Skin irritation - 0.8130 81.30%
Skin corrosion - 0.9444 94.44%
Ames mutagenesis + 0.5836 58.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5818 58.18%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8549 85.49%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6302 63.02%
Acute Oral Toxicity (c) III 0.5704 57.04%
Estrogen receptor binding + 0.9006 90.06%
Androgen receptor binding + 0.5725 57.25%
Thyroid receptor binding + 0.6582 65.82%
Glucocorticoid receptor binding + 0.8170 81.70%
Aromatase binding + 0.7612 76.12%
PPAR gamma + 0.8503 85.03%
Honey bee toxicity - 0.8691 86.91%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6651 66.51%
Fish aquatic toxicity + 0.6939 69.39%

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 99.31% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.67% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.60% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.72% 94.00%
CHEMBL2581 P07339 Cathepsin D 93.80% 98.95%
CHEMBL2535 P11166 Glucose transporter 93.50% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.20% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.46% 96.09%
CHEMBL213 P08588 Beta-1 adrenergic receptor 91.01% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.76% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.64% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.79% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 88.56% 93.31%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.54% 92.62%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.54% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.24% 99.23%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 86.20% 81.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.00% 92.94%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 85.32% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 85.06% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.96% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.83% 97.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.47% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.71% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 82.80% 94.73%

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 anisata

Cross-Links

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PubChem 10448976
LOTUS LTS0245025
wikiData Q104400811