Indan

Details

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Internal ID 93e454ce-604e-4d8e-99db-f7bbdda323f0
Taxonomy Benzenoids > Indanes
IUPAC Name 2,3-dihydro-1H-indene
SMILES (Canonical) C1CC2=CC=CC=C2C1
SMILES (Isomeric) C1CC2=CC=CC=C2C1
InChI InChI=1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2
InChI Key PQNFLJBBNBOBRQ-UHFFFAOYSA-N
Popularity 1,368 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10
Molecular Weight 118.18 g/mol
Exact Mass 118.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Indane
2,3-Dihydro-1H-indene
496-11-7
Hydrindene
1H-Indene, 2,3-dihydro-
Benzocyclopentane
2,3-Dihydroindene
1,2-Hydrindene
Hydrindonaphthene
Indene, 2,3-dihydro-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Indan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9816 98.16%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Lysosomes 0.6992 69.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9708 97.08%
OATP1B3 inhibitior + 0.9686 96.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9149 91.49%
P-glycoprotein inhibitior - 0.9893 98.93%
P-glycoprotein substrate - 0.9946 99.46%
CYP3A4 substrate - 0.8062 80.62%
CYP2C9 substrate - 0.8117 81.17%
CYP2D6 substrate + 0.4387 43.87%
CYP3A4 inhibition - 0.9295 92.95%
CYP2C9 inhibition - 0.8213 82.13%
CYP2C19 inhibition - 0.7168 71.68%
CYP2D6 inhibition - 0.8596 85.96%
CYP1A2 inhibition + 0.6498 64.98%
CYP2C8 inhibition - 0.9902 99.02%
CYP inhibitory promiscuity - 0.5863 58.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.4534 45.34%
Eye corrosion + 0.8780 87.80%
Eye irritation + 0.9971 99.71%
Skin irritation + 0.8958 89.58%
Skin corrosion - 0.9339 93.39%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6575 65.75%
Micronuclear - 0.9284 92.84%
Hepatotoxicity + 0.6694 66.94%
skin sensitisation + 0.8590 85.90%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.5923 59.23%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.7080 70.80%
Acute Oral Toxicity (c) III 0.5493 54.93%
Estrogen receptor binding - 0.8913 89.13%
Androgen receptor binding - 0.7019 70.19%
Thyroid receptor binding - 0.8661 86.61%
Glucocorticoid receptor binding - 0.9004 90.04%
Aromatase binding - 0.8141 81.41%
PPAR gamma - 0.8649 86.49%
Honey bee toxicity - 0.9626 96.26%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.9000 90.00%
Fish aquatic toxicity + 0.9413 94.13%

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 91.97% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.65% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.00% 93.99%
CHEMBL1951 P21397 Monoamine oxidase A 84.24% 91.49%
CHEMBL2581 P07339 Cathepsin D 82.44% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.26% 94.62%

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.
Artemisia argyi
Crocus sativus

Cross-Links

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PubChem 10326
NPASS NPC21211