Clauraila B

Details

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Internal ID 20f2b21c-c6b1-480c-8bc7-169304222d47
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 3,3,5-trimethyl-11H-pyrano[3,2-a]carbazol-10-ol
SMILES (Canonical) CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C2C=CC=C4O
SMILES (Isomeric) CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C2C=CC=C4O
InChI InChI=1S/C18H17NO2/c1-10-9-13-11-5-4-6-14(20)16(11)19-15(13)12-7-8-18(2,3)21-17(10)12/h4-9,19-20H,1-3H3
InChI Key DOPPWRJNMKMWAZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H17NO2
Molecular Weight 279.30 g/mol
Exact Mass 279.125928785 g/mol
Topological Polar Surface Area (TPSA) 45.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.52
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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CHEBI:69923
Claurailas B
CHEMBL1689796
Q27138267

2D Structure

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2D Structure of Clauraila B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.5910 59.10%
Blood Brain Barrier + 0.6379 63.79%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6654 66.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9050 90.50%
OATP1B3 inhibitior + 0.9560 95.60%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7370 73.70%
P-glycoprotein inhibitior - 0.6692 66.92%
P-glycoprotein substrate - 0.6717 67.17%
CYP3A4 substrate + 0.5842 58.42%
CYP2C9 substrate + 0.6173 61.73%
CYP2D6 substrate - 0.7270 72.70%
CYP3A4 inhibition - 0.8558 85.58%
CYP2C9 inhibition + 0.6177 61.77%
CYP2C19 inhibition + 0.6603 66.03%
CYP2D6 inhibition - 0.7063 70.63%
CYP1A2 inhibition + 0.6916 69.16%
CYP2C8 inhibition + 0.6274 62.74%
CYP inhibitory promiscuity + 0.7428 74.28%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4999 49.99%
Eye corrosion - 0.9935 99.35%
Eye irritation + 0.6778 67.78%
Skin irritation - 0.8229 82.29%
Skin corrosion - 0.9394 93.94%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5319 53.19%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5564 55.64%
skin sensitisation - 0.7389 73.89%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8311 83.11%
Acute Oral Toxicity (c) III 0.6558 65.58%
Estrogen receptor binding + 0.9473 94.73%
Androgen receptor binding + 0.7726 77.26%
Thyroid receptor binding + 0.9189 91.89%
Glucocorticoid receptor binding + 0.9436 94.36%
Aromatase binding + 0.9051 90.51%
PPAR gamma + 0.7382 73.82%
Honey bee toxicity - 0.9216 92.16%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.6862 68.62%

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 98.44% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 97.44% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.49% 93.99%
CHEMBL1951 P21397 Monoamine oxidase A 94.66% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.80% 94.45%
CHEMBL2581 P07339 Cathepsin D 92.48% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.09% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.93% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 90.62% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.11% 99.15%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.72% 93.40%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.85% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.41% 96.09%
CHEMBL2535 P11166 Glucose transporter 85.10% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.03% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.66% 99.23%
CHEMBL213 P08588 Beta-1 adrenergic receptor 83.64% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.80% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.96% 94.80%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.62% 91.71%
CHEMBL1907 P15144 Aminopeptidase N 81.47% 93.31%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.00% 93.56%

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 harmandiana

Cross-Links

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PubChem 51039826
LOTUS LTS0187519
wikiData Q27138267