Pterosinf

Details

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Internal ID 9aaff109-b993-40c9-96df-244b4f2e275b
Taxonomy Benzenoids > Indanes > Indanones
IUPAC Name (2R)-6-(2-chloroethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one
SMILES (Canonical) CC1CC2=C(C1=O)C(=C(C(=C2)C)CCCl)C
SMILES (Isomeric) C[C@@H]1CC2=C(C1=O)C(=C(C(=C2)C)CCCl)C
InChI InChI=1S/C14H17ClO/c1-8-6-11-7-9(2)14(16)13(11)10(3)12(8)4-5-15/h6,9H,4-5,7H2,1-3H3/t9-/m1/s1
InChI Key DFJCTWMNTSWCRI-SECBINFHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H17ClO
Molecular Weight 236.73 g/mol
Exact Mass 236.0967929 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.46
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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C14H17ClO
C14-H17-Cl-O

2D Structure

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2D Structure of Pterosinf

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 + 0.9460 94.60%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.5690 56.90%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9191 91.91%
OATP1B3 inhibitior + 0.9528 95.28%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6063 60.63%
P-glycoprotein inhibitior - 0.9385 93.85%
P-glycoprotein substrate - 0.8186 81.86%
CYP3A4 substrate + 0.5138 51.38%
CYP2C9 substrate - 0.8092 80.92%
CYP2D6 substrate - 0.7933 79.33%
CYP3A4 inhibition - 0.8843 88.43%
CYP2C9 inhibition - 0.7616 76.16%
CYP2C19 inhibition - 0.7135 71.35%
CYP2D6 inhibition - 0.8823 88.23%
CYP1A2 inhibition + 0.8459 84.59%
CYP2C8 inhibition - 0.9445 94.45%
CYP inhibitory promiscuity - 0.7881 78.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7444 74.44%
Carcinogenicity (trinary) Non-required 0.6184 61.84%
Eye corrosion - 0.7990 79.90%
Eye irritation + 0.5316 53.16%
Skin irritation + 0.5186 51.86%
Skin corrosion + 0.5276 52.76%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7063 70.63%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.8291 82.91%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.5725 57.25%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6995 69.95%
Acute Oral Toxicity (c) III 0.5914 59.14%
Estrogen receptor binding - 0.7690 76.90%
Androgen receptor binding + 0.5495 54.95%
Thyroid receptor binding - 0.5646 56.46%
Glucocorticoid receptor binding - 0.6768 67.68%
Aromatase binding - 0.8308 83.08%
PPAR gamma - 0.6140 61.40%
Honey bee toxicity - 0.9218 92.18%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9690 96.90%

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
CHEMBL2581 P07339 Cathepsin D 94.34% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 93.20% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.20% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.06% 95.56%
CHEMBL240 Q12809 HERG 89.59% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.06% 86.33%
CHEMBL4208 P20618 Proteasome component C5 86.51% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.55% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 82.40% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.06% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.05% 93.40%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.59% 94.00%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 80.70% 81.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.63% 96.95%

Cross-Links

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PubChem 46849741
NPASS NPC125675
LOTUS LTS0231717
wikiData Q104977917