Indene

Details

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Internal ID 8594db22-7cca-4650-926b-fcb251dbf94b
Taxonomy Benzenoids > Indenes and isoindenes
IUPAC Name 1H-indene
SMILES (Canonical) C1C=CC2=CC=CC=C21
SMILES (Isomeric) C1C=CC2=CC=CC=C21
InChI InChI=1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
InChI Key YBYIRNPNPLQARY-UHFFFAOYSA-N
Popularity 3,872 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8
Molecular Weight 116.16 g/mol
Exact Mass 116.062600255 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1H-Indene
95-13-6
Indonaphthene
Inden
Indenyl radical
HSDB 5286
NSC 9270
EINECS 202-393-6
UNII-67H8Y6LB8A
67H8Y6LB8A
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Indene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.9749 97.49%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.7114 71.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9690 96.90%
OATP1B3 inhibitior + 0.9689 96.89%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8836 88.36%
P-glycoprotein inhibitior - 0.9902 99.02%
P-glycoprotein substrate - 0.9711 97.11%
CYP3A4 substrate - 0.6669 66.69%
CYP2C9 substrate - 0.8094 80.94%
CYP2D6 substrate + 0.3482 34.82%
CYP3A4 inhibition - 0.8788 87.88%
CYP2C9 inhibition - 0.7868 78.68%
CYP2C19 inhibition - 0.5988 59.88%
CYP2D6 inhibition - 0.8431 84.31%
CYP1A2 inhibition + 0.6892 68.92%
CYP2C8 inhibition - 0.9774 97.74%
CYP inhibitory promiscuity + 0.5359 53.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6419 64.19%
Carcinogenicity (trinary) Warning 0.4454 44.54%
Eye corrosion + 0.9014 90.14%
Eye irritation + 0.9971 99.71%
Skin irritation + 0.9495 94.95%
Skin corrosion - 0.7798 77.98%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7534 75.34%
Micronuclear - 0.8319 83.19%
Hepatotoxicity + 0.9000 90.00%
skin sensitisation + 0.9613 96.13%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5103 51.03%
Acute Oral Toxicity (c) III 0.8369 83.69%
Estrogen receptor binding - 0.8699 86.99%
Androgen receptor binding - 0.8277 82.77%
Thyroid receptor binding - 0.8947 89.47%
Glucocorticoid receptor binding - 0.8835 88.35%
Aromatase binding - 0.7406 74.06%
PPAR gamma - 0.8546 85.46%
Honey bee toxicity - 0.9396 93.96%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.9200 92.00%
Fish aquatic toxicity + 0.9703 97.03%

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 90.12% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.99% 95.56%
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 84.69% 92.17%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 84.56% 81.29%
CHEMBL240 Q12809 HERG 82.28% 89.76%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.61% 94.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.00% 93.99%

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.
Elsholtzia ciliata
Mosla chinensis
Terminalia chebula
Vaccinium macrocarpon

Cross-Links

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PubChem 7219
NPASS NPC66517
LOTUS LTS0077189
wikiData Q421008