cis-Hydrindane

Details

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Internal ID 81a7277f-e49d-4e82-9a3c-be3ae00f86ea
Taxonomy Hydrocarbons > Polycyclic hydrocarbons
IUPAC Name (3aS,7aR)-2,3,3a,4,5,6,7,7a-octahydro-1H-indene
SMILES (Canonical) C1CCC2CCCC2C1
SMILES (Isomeric) C1CC[C@H]2CCC[C@H]2C1
InChI InChI=1S/C9H16/c1-2-5-9-7-3-6-8(9)4-1/h8-9H,1-7H2/t8-,9+
InChI Key BNRNAKTVFSZAFA-DTORHVGOSA-N
Popularity 67 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16
Molecular Weight 124.22 g/mol
Exact Mass 124.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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4551-51-3
cis-Hydrindan
cis-Perhydroindene
(3aR,7aS)-octahydro-1H-indene
Octahydro-1H-indene, cis-
8SZ801C84W
CHEBI:49306
RefChem:879141
rel-(3aR,7aS)-Octahydro-1H-indene
679-906-9
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of cis-Hydrindane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.5748 57.48%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.7888 78.88%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9764 97.64%
OATP1B3 inhibitior + 0.9694 96.94%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9386 93.86%
P-glycoprotein inhibitior - 0.9845 98.45%
P-glycoprotein substrate - 0.9939 99.39%
CYP3A4 substrate - 0.7915 79.15%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate + 0.3521 35.21%
CYP3A4 inhibition - 0.9585 95.85%
CYP2C9 inhibition - 0.9249 92.49%
CYP2C19 inhibition - 0.9154 91.54%
CYP2D6 inhibition - 0.9517 95.17%
CYP1A2 inhibition - 0.7048 70.48%
CYP2C8 inhibition - 0.9891 98.91%
CYP inhibitory promiscuity - 0.7855 78.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Warning 0.4580 45.80%
Eye corrosion + 0.9618 96.18%
Eye irritation + 0.9958 99.58%
Skin irritation + 0.8022 80.22%
Skin corrosion - 0.8053 80.53%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5854 58.54%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7157 71.57%
skin sensitisation + 0.8085 80.85%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5552 55.52%
Acute Oral Toxicity (c) IV 0.6361 63.61%
Estrogen receptor binding - 0.9292 92.92%
Androgen receptor binding - 0.7391 73.91%
Thyroid receptor binding - 0.8831 88.31%
Glucocorticoid receptor binding - 0.8863 88.63%
Aromatase binding - 0.8227 82.27%
PPAR gamma - 0.9338 93.38%
Honey bee toxicity - 0.9139 91.39%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.9000 90.00%
Fish aquatic toxicity + 0.8895 88.95%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 86.61% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.32% 99.18%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.13% 97.25%
CHEMBL237 P41145 Kappa opioid receptor 82.42% 98.10%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.90% 92.94%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.38% 93.04%
CHEMBL3012 Q13946 Phosphodiesterase 7A 80.26% 99.29%

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.
Nerium oleander

Cross-Links

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PubChem 643587
NPASS NPC180941