Bicyclo[3.2.0]hept-6-ene

Details

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Internal ID 6e050097-f652-45a7-9181-364d0da8ff3b
Taxonomy Hydrocarbons > Polycyclic hydrocarbons
IUPAC Name bicyclo[3.2.0]hept-6-ene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H10/c1-2-6-4-5-7(6)3-1/h4-7H,1-3H2
InChI Key LMULYBMQCQUKHQ-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10
Molecular Weight 94.15 g/mol
Exact Mass 94.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Bicyclo(3.2.0)hept-6-ene
4927-03-1
DTXSID60964194
RefChem:119717
DTXCID301391900
LMULYBMQCQUKHQ-UHFFFAOYSA-N
SCHEMBL1047645
SCHEMBL6519494
SCHEMBL9777832

2D Structure

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2D Structure of Bicyclo[3.2.0]hept-6-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9868 98.68%
Caco-2 + 0.6646 66.46%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.6515 65.15%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9688 96.88%
OATP1B3 inhibitior + 0.9603 96.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9453 94.53%
P-glycoprotein inhibitior - 0.9845 98.45%
P-glycoprotein substrate - 0.9908 99.08%
CYP3A4 substrate - 0.7817 78.17%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.7008 70.08%
CYP3A4 inhibition - 0.9448 94.48%
CYP2C9 inhibition - 0.8875 88.75%
CYP2C19 inhibition - 0.8662 86.62%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition - 0.6565 65.65%
CYP2C8 inhibition - 0.9835 98.35%
CYP inhibitory promiscuity - 0.7897 78.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Warning 0.4103 41.03%
Eye corrosion + 0.9168 91.68%
Eye irritation + 0.9608 96.08%
Skin irritation + 0.8151 81.51%
Skin corrosion - 0.9328 93.28%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6597 65.97%
Micronuclear - 0.9858 98.58%
Hepatotoxicity + 0.7407 74.07%
skin sensitisation + 0.7112 71.12%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.4768 47.68%
Acute Oral Toxicity (c) III 0.6192 61.92%
Estrogen receptor binding - 0.9194 91.94%
Androgen receptor binding - 0.8917 89.17%
Thyroid receptor binding - 0.8823 88.23%
Glucocorticoid receptor binding - 0.8062 80.62%
Aromatase binding - 0.8840 88.40%
PPAR gamma - 0.9075 90.75%
Honey bee toxicity - 0.8857 88.57%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.8520 85.20%

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 88.45% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.42% 92.94%

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.
Cyperus rotundus

Cross-Links

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PubChem 138390
NPASS NPC124502
LOTUS LTS0249094
wikiData Q82946127