Heptane, 4-methylene-

Details

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Internal ID 2b4dd5b7-f408-4022-a579-0812b71d9cfe
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 4-methylideneheptane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H16/c1-4-6-8(3)7-5-2/h3-7H2,1-2H3
InChI Key FYUUBXZYRPRIHC-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16
Molecular Weight 112.21 g/mol
Exact Mass 112.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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2-Propyl-1-pentene
4-methylideneheptane
1-Pentene, 2-propyl-
15918-08-8
2-Propylpent-1-ene
DTXSID70333913
FYUUBXZYRPRIHC-UHFFFAOYSA-N
AKOS013992403

2D Structure

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2D Structure of Heptane, 4-methylene-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9857 98.57%
Caco-2 + 0.9789 97.89%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.4138 41.38%
OATP2B1 inhibitior - 0.8338 83.38%
OATP1B1 inhibitior + 0.9336 93.36%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9405 94.05%
P-glycoprotein inhibitior - 0.9833 98.33%
P-glycoprotein substrate - 0.9697 96.97%
CYP3A4 substrate - 0.7429 74.29%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9479 94.79%
CYP2C9 inhibition - 0.9176 91.76%
CYP2C19 inhibition - 0.9150 91.50%
CYP2D6 inhibition - 0.9310 93.10%
CYP1A2 inhibition - 0.6312 63.12%
CYP2C8 inhibition - 0.9853 98.53%
CYP inhibitory promiscuity - 0.5648 56.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Warning 0.5319 53.19%
Eye corrosion + 0.8536 85.36%
Eye irritation + 0.9886 98.86%
Skin irritation + 0.6461 64.61%
Skin corrosion - 0.9956 99.56%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6161 61.61%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7627 76.27%
skin sensitisation + 0.9491 94.91%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6363 63.63%
Acute Oral Toxicity (c) III 0.8652 86.52%
Estrogen receptor binding - 0.9782 97.82%
Androgen receptor binding - 0.9307 93.07%
Thyroid receptor binding - 0.8721 87.21%
Glucocorticoid receptor binding - 0.9140 91.40%
Aromatase binding - 0.8997 89.97%
PPAR gamma - 0.9455 94.55%
Honey bee toxicity - 0.9516 95.16%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.5232 52.32%
Fish aquatic toxicity + 0.9933 99.33%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.05% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.62% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 80.84% 87.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.37% 97.25%

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

Cross-Links

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PubChem 519193
LOTUS LTS0110917
wikiData Q82099486