1H-Indene, 1-methylene-

Details

Top
Internal ID 9e86729c-d9d2-4674-a4ed-45df142f0902
Taxonomy Benzenoids > Indenes and isoindenes
IUPAC Name 1-methylideneindene
SMILES (Canonical) C=C1C=CC2=CC=CC=C12
SMILES (Isomeric) C=C1C=CC2=CC=CC=C12
InChI InChI=1S/C10H8/c1-8-6-7-9-4-2-3-5-10(8)9/h2-7H,1H2
InChI Key HVVZVBWIBBTXAJ-UHFFFAOYSA-N
Popularity 40 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H8
Molecular Weight 128.17 g/mol
Exact Mass 128.062600255 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
1-Methylene-1H-indene
2471-84-3
1-methylideneindene
benzofulvene
1-methylidene-1H-indene
DTXSID20179449
HVVZVBWIBBTXAJ-UHFFFAOYSA-N
111307-68-7

2D Structure

Top
2D Structure of 1H-Indene, 1-methylene-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.9619 96.19%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Lysosomes 0.7171 71.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9494 94.94%
OATP1B3 inhibitior + 0.9580 95.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8482 84.82%
P-glycoprotein inhibitior - 0.9788 97.88%
P-glycoprotein substrate - 0.9645 96.45%
CYP3A4 substrate - 0.6553 65.53%
CYP2C9 substrate - 0.6241 62.41%
CYP2D6 substrate - 0.7140 71.40%
CYP3A4 inhibition - 0.7433 74.33%
CYP2C9 inhibition - 0.7334 73.34%
CYP2C19 inhibition - 0.5122 51.22%
CYP2D6 inhibition - 0.7291 72.91%
CYP1A2 inhibition + 0.6794 67.94%
CYP2C8 inhibition - 0.8946 89.46%
CYP inhibitory promiscuity + 0.7192 71.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6319 63.19%
Carcinogenicity (trinary) Non-required 0.4654 46.54%
Eye corrosion + 0.7344 73.44%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8588 85.88%
Skin corrosion - 0.8328 83.28%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7489 74.89%
Micronuclear - 0.8419 84.19%
Hepatotoxicity + 0.9125 91.25%
skin sensitisation + 0.9444 94.44%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7450 74.50%
Acute Oral Toxicity (c) III 0.6879 68.79%
Estrogen receptor binding - 0.7232 72.32%
Androgen receptor binding - 0.5363 53.63%
Thyroid receptor binding - 0.7254 72.54%
Glucocorticoid receptor binding - 0.8613 86.13%
Aromatase binding - 0.7413 74.13%
PPAR gamma - 0.6030 60.30%
Honey bee toxicity - 0.8789 87.89%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.8300 83.00%
Fish aquatic toxicity + 0.9916 99.16%

Targets

Top

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
CHEMBL1951 P21397 Monoamine oxidase A 96.69% 91.49%
CHEMBL2581 P07339 Cathepsin D 88.62% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.10% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.76% 91.11%
CHEMBL240 Q12809 HERG 81.88% 89.76%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.04% 93.81%

Plants that contains it

Top
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.
Ficus carica
Melia azedarach

Cross-Links

Top
PubChem 75581
NPASS NPC5642