5,6-Dipropyldecane

Details

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Internal ID 2b8ccbd8-6f04-45d7-875f-b1e6907fa7af
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 5,6-dipropyldecane
SMILES (Canonical) CCCCC(CCC)C(CCC)CCCC
SMILES (Isomeric) CCCCC(CCC)C(CCC)CCCC
InChI InChI=1S/C16H34/c1-5-9-13-15(11-7-3)16(12-8-4)14-10-6-2/h15-16H,5-14H2,1-4H3
InChI Key AHCQADSOCBSROH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H34
Molecular Weight 226.44 g/mol
Exact Mass 226.266051085 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.30
Atomic LogP (AlogP) 6.20
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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Decane, 5,6-dipropyl-
5,6-Dipropyldecane #
AHCQADSOCBSROH-UHFFFAOYSA-N

2D Structure

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2D Structure of 5,6-Dipropyldecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9552 95.52%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.5432 54.32%
OATP2B1 inhibitior - 0.8420 84.20%
OATP1B1 inhibitior + 0.9510 95.10%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8714 87.14%
P-glycoprotein inhibitior - 0.9229 92.29%
P-glycoprotein substrate - 0.9023 90.23%
CYP3A4 substrate - 0.7329 73.29%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9842 98.42%
CYP2C9 inhibition - 0.9267 92.67%
CYP2C19 inhibition - 0.9483 94.83%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition - 0.6549 65.49%
CYP2C8 inhibition - 0.9867 98.67%
CYP inhibitory promiscuity - 0.7959 79.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6062 60.62%
Eye corrosion + 0.9906 99.06%
Eye irritation + 0.9724 97.24%
Skin irritation + 0.8624 86.24%
Skin corrosion - 0.9704 97.04%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4638 46.38%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.9268 92.68%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.9086 90.86%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity + 0.6096 60.96%
Acute Oral Toxicity (c) III 0.5369 53.69%
Estrogen receptor binding - 0.6588 65.88%
Androgen receptor binding - 0.7018 70.18%
Thyroid receptor binding - 0.6248 62.48%
Glucocorticoid receptor binding - 0.8751 87.51%
Aromatase binding - 0.8644 86.44%
PPAR gamma - 0.8051 80.51%
Honey bee toxicity - 0.9749 97.49%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9752 97.52%

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
CHEMBL1907 P15144 Aminopeptidase N 94.13% 93.31%
CHEMBL2581 P07339 Cathepsin D 93.61% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.00% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 87.77% 91.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.44% 96.09%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 86.03% 95.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.21% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.11% 99.17%
CHEMBL2996 Q05655 Protein kinase C delta 81.91% 97.79%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.07% 85.94%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.84% 92.08%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.48% 93.56%

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.
Nelumbo nucifera

Cross-Links

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PubChem 518459
NPASS NPC293700