Carexane D

Details

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Internal ID b345fb8e-6567-46a5-b06b-69ff1fd40012
Taxonomy Benzenoids > Fluorenes
IUPAC Name (4bR,10aR)-9-hydroxy-7-methoxy-11,11-dimethyl-10,10a-dihydro-4bH-benzo[b]fluoren-5-one
SMILES (Canonical) CC1(C2CC3=C(C=C(C=C3O)OC)C(=O)C2C4=CC=CC=C41)C
SMILES (Isomeric) CC1([C@@H]2CC3=C(C=C(C=C3O)OC)C(=O)[C@H]2C4=CC=CC=C41)C
InChI InChI=1S/C20H20O3/c1-20(2)15-7-5-4-6-12(15)18-16(20)10-13-14(19(18)22)8-11(23-3)9-17(13)21/h4-9,16,18,21H,10H2,1-3H3/t16-,18+/m1/s1
InChI Key YFNNKWLFVPQLOR-AEFFLSMTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O3
Molecular Weight 308.40 g/mol
Exact Mass 308.14124450 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 3
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 Carexane D

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 + 0.7796 77.96%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8488 84.88%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.8717 87.17%
OATP1B3 inhibitior + 0.9521 95.21%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4667 46.67%
P-glycoprotein inhibitior - 0.5889 58.89%
P-glycoprotein substrate - 0.8087 80.87%
CYP3A4 substrate + 0.6630 66.30%
CYP2C9 substrate - 0.7818 78.18%
CYP2D6 substrate - 0.7633 76.33%
CYP3A4 inhibition - 0.8872 88.72%
CYP2C9 inhibition - 0.6485 64.85%
CYP2C19 inhibition - 0.5147 51.47%
CYP2D6 inhibition - 0.8987 89.87%
CYP1A2 inhibition + 0.6937 69.37%
CYP2C8 inhibition + 0.6901 69.01%
CYP inhibitory promiscuity - 0.7491 74.91%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8233 82.33%
Carcinogenicity (trinary) Non-required 0.5170 51.70%
Eye corrosion - 0.9849 98.49%
Eye irritation - 0.7912 79.12%
Skin irritation - 0.7049 70.49%
Skin corrosion - 0.9753 97.53%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6692 66.92%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8671 86.71%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.6513 65.13%
Acute Oral Toxicity (c) III 0.6017 60.17%
Estrogen receptor binding + 0.8483 84.83%
Androgen receptor binding + 0.7186 71.86%
Thyroid receptor binding + 0.6229 62.29%
Glucocorticoid receptor binding + 0.7069 70.69%
Aromatase binding + 0.6179 61.79%
PPAR gamma + 0.7581 75.81%
Honey bee toxicity - 0.8802 88.02%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9841 98.41%

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 99.70% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.28% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.84% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.99% 96.09%
CHEMBL2535 P11166 Glucose transporter 95.34% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.60% 99.15%
CHEMBL2581 P07339 Cathepsin D 90.51% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.09% 86.33%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 89.21% 92.67%
CHEMBL240 Q12809 HERG 87.73% 89.76%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.69% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.06% 82.69%
CHEMBL1907 P15144 Aminopeptidase N 84.97% 93.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.86% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.65% 97.09%
CHEMBL4208 P20618 Proteasome component C5 83.44% 90.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.77% 92.68%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.73% 93.40%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.68% 91.07%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.66% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.53% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.20% 92.62%

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.
Carex distachya

Cross-Links

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PubChem 11630932
LOTUS LTS0046876
wikiData Q105347697