Ectocarpene

Details

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Internal ID 8cd37d70-1ae8-4e75-baf3-2d53c34559be
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Cyclic olefins > Cycloalkenes
IUPAC Name (6R)-6-[(E)-but-1-enyl]cyclohepta-1,4-diene
SMILES (Canonical) CCC=CC1CC=CCC=C1
SMILES (Isomeric) CC/C=C/[C@H]1CC=CCC=C1
InChI InChI=1S/C11H16/c1-2-3-8-11-9-6-4-5-7-10-11/h3-4,6-8,10-11H,2,5,9H2,1H3/b8-3+/t11-/m0/s1
InChI Key KIFXGGYCNMHCSX-AEBAWRHJSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16
Molecular Weight 148.24 g/mol
Exact Mass 148.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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1-(1-Butenyl)-2,5-cycloheptadiene
33156-93-3
5LT5CQ3SYJ
1,4-Cycloheptadiene, 6-(1-butenyl)-, [S-(Z)]-
Dictyopteren D'
Dictyopterene D'
(6R)-6-[(E)-but-1-enyl]cyclohepta-1,4-diene
(R)-6-(1-Butenyl)-1,4-cycloheptadiene
Sirenin (Etocarpus)
UNII-5LT5CQ3SYJ
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ectocarpene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.8961 89.61%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4407 44.07%
OATP2B1 inhibitior - 0.8688 86.88%
OATP1B1 inhibitior + 0.9155 91.55%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8404 84.04%
P-glycoprotein inhibitior - 0.9818 98.18%
P-glycoprotein substrate - 0.9055 90.55%
CYP3A4 substrate - 0.6275 62.75%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.7561 75.61%
CYP3A4 inhibition - 0.9701 97.01%
CYP2C9 inhibition - 0.8571 85.71%
CYP2C19 inhibition - 0.9060 90.60%
CYP2D6 inhibition - 0.9396 93.96%
CYP1A2 inhibition - 0.6819 68.19%
CYP2C8 inhibition - 0.9278 92.78%
CYP inhibitory promiscuity - 0.6524 65.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.4617 46.17%
Eye corrosion + 0.9774 97.74%
Eye irritation + 0.9669 96.69%
Skin irritation + 0.8161 81.61%
Skin corrosion - 0.7968 79.68%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5550 55.50%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.9114 91.14%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6904 69.04%
Acute Oral Toxicity (c) III 0.8118 81.18%
Estrogen receptor binding - 0.8889 88.89%
Androgen receptor binding - 0.9068 90.68%
Thyroid receptor binding - 0.7696 76.96%
Glucocorticoid receptor binding - 0.8410 84.10%
Aromatase binding - 0.8047 80.47%
PPAR gamma - 0.7798 77.98%
Honey bee toxicity - 0.9118 91.18%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9691 96.91%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.79% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.85% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.00% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.94% 97.09%

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.
Capsicum annuum
Pteris quadriaurita

Cross-Links

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PubChem 6440990
NPASS NPC149408
LOTUS LTS0217680
wikiData Q988591