2,2,4,6,6-Pentamethylheptane

Details

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Internal ID 321a91fd-7b41-4c89-9cfe-8db592e33508
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 2,2,4,6,6-pentamethylheptane
SMILES (Canonical) CC(CC(C)(C)C)CC(C)(C)C
SMILES (Isomeric) CC(CC(C)(C)C)CC(C)(C)C
InChI InChI=1S/C12H26/c1-10(8-11(2,3)4)9-12(5,6)7/h10H,8-9H2,1-7H3
InChI Key VKPSKYDESGTTFR-UHFFFAOYSA-N
Popularity 61 references in papers

Physical and Chemical Properties

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Molecular Formula C12H26
Molecular Weight 170.33 g/mol
Exact Mass 170.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.49
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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13475-82-6
Heptane, 2,2,4,6,6-pentamethyl-
UNII-A8289P68Y2
EINECS 236-757-0
A8289P68Y2
EC 236-757-0
2,2,4,6,6-Pentamethylheptane 100 microg/mL in Acetonitrile
2,2,4,6,6-pentamethyl-heptane
Permethyl 99A
PMH cpd
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,2,4,6,6-Pentamethylheptane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9824 98.24%
Caco-2 + 0.7734 77.34%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Lysosomes 0.5734 57.34%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9660 96.60%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8245 82.45%
P-glycoprotein inhibitior - 0.9652 96.52%
P-glycoprotein substrate - 0.9549 95.49%
CYP3A4 substrate - 0.7776 77.76%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7490 74.90%
CYP3A4 inhibition - 0.9151 91.51%
CYP2C9 inhibition - 0.9339 93.39%
CYP2C19 inhibition - 0.9571 95.71%
CYP2D6 inhibition - 0.9377 93.77%
CYP1A2 inhibition - 0.9082 90.82%
CYP2C8 inhibition - 0.9971 99.71%
CYP inhibitory promiscuity - 0.8808 88.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6383 63.83%
Carcinogenicity (trinary) Warning 0.5248 52.48%
Eye corrosion + 0.9869 98.69%
Eye irritation + 0.9618 96.18%
Skin irritation + 0.8742 87.42%
Skin corrosion - 0.9688 96.88%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8326 83.26%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7927 79.27%
skin sensitisation + 0.8930 89.30%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity + 0.9526 95.26%
Nephrotoxicity + 0.5106 51.06%
Acute Oral Toxicity (c) III 0.7060 70.60%
Estrogen receptor binding - 0.8979 89.79%
Androgen receptor binding - 0.8347 83.47%
Thyroid receptor binding - 0.8144 81.44%
Glucocorticoid receptor binding - 0.8855 88.55%
Aromatase binding - 0.7922 79.22%
PPAR gamma - 0.8812 88.12%
Honey bee toxicity - 0.8964 89.64%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.7671 76.71%

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 94.87% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.13% 98.95%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 84.38% 97.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.82% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 81.33% 93.31%

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.
Combretum indicum
Lycium barbarum
Lycium chinense

Cross-Links

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PubChem 26058
NPASS NPC48747
LOTUS LTS0225155
wikiData Q27147086