Clausevatine D

Details

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Internal ID 67ad4d79-1a93-4b8b-b181-d45f8c3bafb4
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 6-hydroxy-2-(2-hydroxypropan-2-yl)-2,7-dihydro-1H-pyrano[3,4-c]carbazol-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H17NO4/c1-18(2,22)14-8-10-11(17(21)23-14)7-13(20)16-15(10)9-5-3-4-6-12(9)19-16/h3-7,14,19-20,22H,8H2,1-2H3
InChI Key NAEJSIJAZCIUHA-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C18H17NO4
Molecular Weight 311.30 g/mol
Exact Mass 311.11575802 g/mol
Topological Polar Surface Area (TPSA) 82.60 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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6-hydroxy-2-(2-hydroxypropan-2-yl)-2,7-dihydro-1H-pyrano(3,4-c)carbazol-4-one
6-Hydroxy-2-(2-hydroxypropan-2-yl)-2,7-dihydro-1H-pyrano[3,4-c]carbazol-4-one
RefChem:126802
215377-68-7

2D Structure

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2D Structure of Clausevatine D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9607 96.07%
Caco-2 - 0.5681 56.81%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6230 62.30%
OATP2B1 inhibitior - 0.7142 71.42%
OATP1B1 inhibitior + 0.8708 87.08%
OATP1B3 inhibitior + 0.9335 93.35%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5588 55.88%
P-glycoprotein inhibitior - 0.6851 68.51%
P-glycoprotein substrate - 0.7026 70.26%
CYP3A4 substrate + 0.6403 64.03%
CYP2C9 substrate - 0.5816 58.16%
CYP2D6 substrate - 0.8384 83.84%
CYP3A4 inhibition - 0.9695 96.95%
CYP2C9 inhibition - 0.8684 86.84%
CYP2C19 inhibition - 0.8094 80.94%
CYP2D6 inhibition - 0.8480 84.80%
CYP1A2 inhibition - 0.5162 51.62%
CYP2C8 inhibition - 0.6503 65.03%
CYP inhibitory promiscuity - 0.8118 81.18%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5911 59.11%
Eye corrosion - 0.9933 99.33%
Eye irritation - 0.7287 72.87%
Skin irritation - 0.7813 78.13%
Skin corrosion - 0.9310 93.10%
Ames mutagenesis + 0.5436 54.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5161 51.61%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.7944 79.44%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.6689 66.89%
Acute Oral Toxicity (c) III 0.5827 58.27%
Estrogen receptor binding + 0.9187 91.87%
Androgen receptor binding + 0.5912 59.12%
Thyroid receptor binding + 0.5725 57.25%
Glucocorticoid receptor binding + 0.8895 88.95%
Aromatase binding + 0.7589 75.89%
PPAR gamma + 0.8803 88.03%
Honey bee toxicity - 0.9239 92.39%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7971 79.71%

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 99.62% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.13% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.87% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.64% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.62% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.02% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.57% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.04% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 89.77% 94.73%
CHEMBL217 P14416 Dopamine D2 receptor 89.16% 95.62%
CHEMBL2535 P11166 Glucose transporter 88.45% 98.75%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 88.06% 81.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.89% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.64% 94.45%
CHEMBL1907 P15144 Aminopeptidase N 85.77% 93.31%
CHEMBL213 P08588 Beta-1 adrenergic receptor 85.23% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.57% 97.09%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 84.08% 85.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.31% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.69% 86.33%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.67% 96.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.21% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.10% 95.89%

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

Cross-Links

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PubChem 10686461
LOTUS LTS0022685
wikiData Q105176195