Santene

Details

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Internal ID 7c160d2f-6d31-4f53-923d-dd203e1b16e9
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 2,3-dimethylbicyclo[2.2.1]hept-2-ene
SMILES (Canonical) CC1=C(C2CCC1C2)C
SMILES (Isomeric) CC1=C(C2CCC1C2)C
InChI InChI=1S/C9H14/c1-6-7(2)9-4-3-8(6)5-9/h8-9H,3-5H2,1-2H3
InChI Key LSIXBBPOJBJQHN-UHFFFAOYSA-N
Popularity 1,307 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14
Molecular Weight 122.21 g/mol
Exact Mass 122.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.75
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Santen
2,3-Dimethylbicyclo[2.2.1]hept-2-ene
529-16-8
2-Norbornene, 2,3-dimethyl-
2,3-dimethyl-2-norbornene
2,3-Dimethylbicyclo(2.2.1)hept-2-ene
2,3-Dimethyl-Bicyclo(2.2.1)hept-2-ene
2,3-dimethyl-bicyclo[2.2.1]hept-2-ene
Bicyclo(2.2.1)hept-2-ene, 2,3-dimethyl-
Bicyclo[2.2.1]hept-2-ene, 2,3-dimethyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Santene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.7460 74.60%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.9286 92.86%
Subcellular localzation Lysosomes 0.7867 78.67%
OATP2B1 inhibitior - 0.8445 84.45%
OATP1B1 inhibitior + 0.9817 98.17%
OATP1B3 inhibitior + 0.9357 93.57%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8960 89.60%
P-glycoprotein inhibitior - 0.9811 98.11%
P-glycoprotein substrate - 0.9536 95.36%
CYP3A4 substrate - 0.7236 72.36%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7697 76.97%
CYP3A4 inhibition - 0.9206 92.06%
CYP2C9 inhibition - 0.9148 91.48%
CYP2C19 inhibition - 0.8116 81.16%
CYP2D6 inhibition - 0.9186 91.86%
CYP1A2 inhibition - 0.6003 60.03%
CYP2C8 inhibition - 0.9740 97.40%
CYP inhibitory promiscuity - 0.5973 59.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.4275 42.75%
Eye corrosion - 0.6100 61.00%
Eye irritation + 0.9732 97.32%
Skin irritation + 0.7041 70.41%
Skin corrosion - 0.9692 96.92%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7412 74.12%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.5757 57.57%
Acute Oral Toxicity (c) IV 0.5177 51.77%
Estrogen receptor binding - 0.8603 86.03%
Androgen receptor binding - 0.6854 68.54%
Thyroid receptor binding - 0.8302 83.02%
Glucocorticoid receptor binding - 0.8347 83.47%
Aromatase binding - 0.7898 78.98%
PPAR gamma - 0.7893 78.93%
Honey bee toxicity - 0.9493 94.93%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.8600 86.00%
Fish aquatic toxicity + 0.9900 99.00%

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 88.23% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.18% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.57% 97.25%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 80.45% 94.55%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 80.05% 95.58%

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.
Abies alba
Abies sachalinensis
Abies sibirica
Chaerophyllum macrospermum
Larix sibirica
Pinus sylvestris
Rhodiola rosea

Cross-Links

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PubChem 10720
LOTUS LTS0105576
wikiData Q104253388