Pentane

Details

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Internal ID f2283b4e-98d9-422e-84ff-9f2716a36538
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name pentane
SMILES (Canonical) CCCCC
SMILES (Isomeric) CCCCC
InChI InChI=1S/C5H12/c1-3-5-4-2/h3-5H2,1-2H3
InChI Key OFBQJSOFQDEBGM-UHFFFAOYSA-N
Popularity 20,208 references in papers

Physical and Chemical Properties

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Molecular Formula C5H12
Molecular Weight 72.15 g/mol
Exact Mass 72.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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n-Pentane
109-66-0
Pentan
Skellysolve A
Pentanen
Pentani
Amyl hydride
Pentanes
Tetrafume
Tetrakil
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pentane

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 + 0.9459 94.59%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Lysosomes 0.5619 56.19%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9486 94.86%
OATP1B3 inhibitior + 0.9469 94.69%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9541 95.41%
P-glycoprotein inhibitior - 0.9862 98.62%
P-glycoprotein substrate - 0.9584 95.84%
CYP3A4 substrate - 0.8217 82.17%
CYP2C9 substrate - 0.8415 84.15%
CYP2D6 substrate - 0.7215 72.15%
CYP3A4 inhibition - 0.9889 98.89%
CYP2C9 inhibition - 0.9524 95.24%
CYP2C19 inhibition - 0.9464 94.64%
CYP2D6 inhibition - 0.9430 94.30%
CYP1A2 inhibition - 0.7466 74.66%
CYP2C8 inhibition - 0.9832 98.32%
CYP inhibitory promiscuity - 0.8490 84.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.6079 60.79%
Eye corrosion + 0.9946 99.46%
Eye irritation + 0.9969 99.69%
Skin irritation + 0.8718 87.18%
Skin corrosion - 0.9770 97.70%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7485 74.85%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8377 83.77%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity + 0.8416 84.16%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.6598 65.98%
Acute Oral Toxicity (c) II 0.5752 57.52%
Estrogen receptor binding - 0.9278 92.78%
Androgen receptor binding - 0.8942 89.42%
Thyroid receptor binding - 0.8501 85.01%
Glucocorticoid receptor binding - 0.9336 93.36%
Aromatase binding - 0.9157 91.57%
PPAR gamma - 0.9154 91.54%
Honey bee toxicity - 0.9937 99.37%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity - 0.6252 62.52%
Fish aquatic toxicity + 0.8118 81.18%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 7943.3 nM
Potency
via CMAUP
CHEMBL1963 P16473 Thyroid stimulating hormone receptor 100 nM
100 nM
100 nM
Potency
Potency
Potency
via CMAUP
via CMAUP
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 90.03% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.72% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.19% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 80.35% 93.31%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.13% 92.86%

Cross-Links

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PubChem 8003
NPASS NPC187095
ChEMBL CHEMBL16102