Heptane, 5-ethyl-2-methyl-

Details

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Internal ID e250ef43-aecb-44de-843a-be7baa4045f5
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 5-ethyl-2-methylheptane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H22/c1-5-10(6-2)8-7-9(3)4/h9-10H,5-8H2,1-4H3
InChI Key DGEMPTLPTFNEHJ-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C10H22
Molecular Weight 142.28 g/mol
Exact Mass 142.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.10
Atomic LogP (AlogP) 3.86
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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13475-78-0
2-Methyl-5-ethylheptane
6-Methyl-3-ethylheptane
DTXSID40158933
2Methyl5ethylheptane
5Ethyl2methylheptane
6Methyl3ethylheptane
RefChem:783661
DTXCID0081424
5-ETHYL-2-METHYLHEPTANE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Heptane, 5-ethyl-2-methyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.9292 92.92%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.3794 37.94%
OATP2B1 inhibitior - 0.8387 83.87%
OATP1B1 inhibitior + 0.9478 94.78%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9645 96.45%
P-glycoprotein inhibitior - 0.9784 97.84%
P-glycoprotein substrate - 0.9056 90.56%
CYP3A4 substrate - 0.7502 75.02%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9850 98.50%
CYP2C9 inhibition - 0.9257 92.57%
CYP2C19 inhibition - 0.9460 94.60%
CYP2D6 inhibition - 0.9398 93.98%
CYP1A2 inhibition - 0.6934 69.34%
CYP2C8 inhibition - 0.9939 99.39%
CYP inhibitory promiscuity - 0.8121 81.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5801 58.01%
Eye corrosion + 0.9823 98.23%
Eye irritation + 0.9857 98.57%
Skin irritation + 0.8650 86.50%
Skin corrosion - 0.9772 97.72%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6181 61.81%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7443 74.43%
skin sensitisation + 0.9351 93.51%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity - 0.9148 91.48%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity + 0.4494 44.94%
Acute Oral Toxicity (c) III 0.4925 49.25%
Estrogen receptor binding - 0.8942 89.42%
Androgen receptor binding - 0.8931 89.31%
Thyroid receptor binding - 0.8264 82.64%
Glucocorticoid receptor binding - 0.9076 90.76%
Aromatase binding - 0.8513 85.13%
PPAR gamma - 0.9200 92.00%
Honey bee toxicity - 0.9508 95.08%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9573 95.73%

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 92.91% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.35% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.71% 96.09%
CHEMBL333 P08253 Matrix metalloproteinase-2 82.35% 96.31%
CHEMBL1907 P15144 Aminopeptidase N 81.87% 93.31%
CHEMBL2885 P07451 Carbonic anhydrase III 81.71% 87.45%

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.
Crataegus pinnatifida

Cross-Links

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PubChem 26056
NPASS NPC38878