2-Heptene

Details

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Internal ID d937f98d-d62d-48c2-8c8a-6ac51ada87fa
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Unsaturated aliphatic hydrocarbons
IUPAC Name hept-2-ene
SMILES (Canonical) CCCCC=CC
SMILES (Isomeric) CCCCC=CC
InChI InChI=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3
InChI Key OTTZHAVKAVGASB-UHFFFAOYSA-N
Popularity 63 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14
Molecular Weight 98.19 g/mol
Exact Mass 98.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.75
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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2-HEPTENE
592-77-8
2-C7H14
heptene-2
FT-0623900
FT-0637126
FT-0694223
H0043
D90785
D90859

2D Structure

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2D Structure of 2-Heptene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9592 95.92%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.4386 43.86%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.7932 79.32%
OATP1B3 inhibitior + 0.9264 92.64%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9302 93.02%
P-glycoprotein inhibitior - 0.9894 98.94%
P-glycoprotein substrate - 0.9423 94.23%
CYP3A4 substrate - 0.7278 72.78%
CYP2C9 substrate - 0.8202 82.02%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.9890 98.90%
CYP2C9 inhibition - 0.9426 94.26%
CYP2C19 inhibition - 0.9361 93.61%
CYP2D6 inhibition - 0.9365 93.65%
CYP1A2 inhibition - 0.6167 61.67%
CYP2C8 inhibition - 0.9634 96.34%
CYP inhibitory promiscuity - 0.7259 72.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.5502 55.02%
Eye corrosion + 0.9739 97.39%
Eye irritation + 0.9827 98.27%
Skin irritation + 0.9023 90.23%
Skin corrosion - 0.9395 93.95%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6160 61.60%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6074 60.74%
skin sensitisation + 0.9715 97.15%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7970 79.70%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5736 57.36%
Acute Oral Toxicity (c) III 0.6016 60.16%
Estrogen receptor binding - 0.9583 95.83%
Androgen receptor binding - 0.8713 87.13%
Thyroid receptor binding - 0.8434 84.34%
Glucocorticoid receptor binding - 0.8414 84.14%
Aromatase binding - 0.9208 92.08%
PPAR gamma - 0.8794 87.94%
Honey bee toxicity - 0.9843 98.43%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9342 93.42%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.18% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.90% 99.17%
CHEMBL2581 P07339 Cathepsin D 88.69% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 86.80% 93.31%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.21% 91.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.41% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 82.39% 97.79%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.93% 92.86%
CHEMBL299 P17252 Protein kinase C alpha 81.10% 98.03%

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.
Basella alba
Foeniculum vulgare

Cross-Links

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PubChem 11611
NPASS NPC132162
LOTUS LTS0114247
wikiData Q82002958