(2S)-2-[(2R)-1-chloro-2-hydroxypropan-2-yl]-5-hydroxy-11-methyl-1,2-dihydrofuro[2,3-c]acridin-6-one

Details

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Internal ID 7af95f82-c9da-4722-b7c0-2d4bd848cb02
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Acridines > Acridones
IUPAC Name (2S)-2-[(2R)-1-chloro-2-hydroxypropan-2-yl]-5-hydroxy-11-methyl-1,2-dihydrofuro[2,3-c]acridin-6-one
SMILES (Canonical) CC(CCl)(C1CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O)O
SMILES (Isomeric) C[C@](CCl)([C@@H]1CC2=C(O1)C=C(C3=C2N(C4=CC=CC=C4C3=O)C)O)O
InChI InChI=1S/C19H18ClNO4/c1-19(24,9-20)15-7-11-14(25-15)8-13(22)16-17(11)21(2)12-6-4-3-5-10(12)18(16)23/h3-6,8,15,22,24H,7,9H2,1-2H3/t15-,19-/m0/s1
InChI Key PGOOUZZLZBIMRI-KXBFYZLASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18ClNO4
Molecular Weight 359.80 g/mol
Exact Mass 359.0924357 g/mol
Topological Polar Surface Area (TPSA) 70.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2-[(2R)-1-chloro-2-hydroxypropan-2-yl]-5-hydroxy-11-methyl-1,2-dihydrofuro[2,3-c]acridin-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9803 98.03%
Caco-2 - 0.5583 55.83%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4354 43.54%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8910 89.10%
OATP1B3 inhibitior + 0.9352 93.52%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6251 62.51%
P-glycoprotein inhibitior - 0.6951 69.51%
P-glycoprotein substrate + 0.5083 50.83%
CYP3A4 substrate + 0.6686 66.86%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8423 84.23%
CYP3A4 inhibition - 0.8605 86.05%
CYP2C9 inhibition - 0.8907 89.07%
CYP2C19 inhibition - 0.7067 70.67%
CYP2D6 inhibition - 0.8239 82.39%
CYP1A2 inhibition - 0.5131 51.31%
CYP2C8 inhibition - 0.5893 58.93%
CYP inhibitory promiscuity - 0.8390 83.90%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.4347 43.47%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9212 92.12%
Skin irritation - 0.8059 80.59%
Skin corrosion - 0.9363 93.63%
Ames mutagenesis + 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4593 45.93%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5161 51.61%
skin sensitisation - 0.8391 83.91%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.7946 79.46%
Acute Oral Toxicity (c) III 0.5694 56.94%
Estrogen receptor binding + 0.8039 80.39%
Androgen receptor binding + 0.5859 58.59%
Thyroid receptor binding + 0.7009 70.09%
Glucocorticoid receptor binding + 0.8212 82.12%
Aromatase binding + 0.7720 77.20%
PPAR gamma + 0.8722 87.22%
Honey bee toxicity - 0.8970 89.70%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.8439 84.39%

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 98.52% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.09% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.94% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.92% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.53% 97.25%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.24% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.06% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 94.29% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.15% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.39% 86.33%
CHEMBL3384 Q16512 Protein kinase N1 90.22% 80.71%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 89.55% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 87.93% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.30% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.97% 99.23%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.05% 93.40%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.41% 100.00%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 83.76% 100.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 83.65% 80.78%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.65% 92.62%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 81.96% 96.37%
CHEMBL2535 P11166 Glucose transporter 80.72% 98.75%

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.
Ruta chalepensis
Ruta graveolens
Thamnosma montana

Cross-Links

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PubChem 16040191
LOTUS LTS0052211
wikiData Q105208511