Cyclopentadecane

Details

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Internal ID 1d4bb00f-5fc8-47e4-a14a-9cecf7e78e7d
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name cyclopentadecane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H30/c1-2-4-6-8-10-12-14-15-13-11-9-7-5-3-1/h1-15H2
InChI Key SRONXYPFSAKOGH-UHFFFAOYSA-N
Popularity 45 references in papers

Physical and Chemical Properties

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Molecular Formula C15H30
Molecular Weight 210.40 g/mol
Exact Mass 210.234750957 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.30
Atomic LogP (AlogP) 5.85
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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295-48-7
EINECS 206-040-7
DTXSID1059781
RefChem:129831
DTXCID8038013
InChI=1/C15H30/c1-2-4-6-8-10-12-14-15-13-11-9-7-5-3-1/h1-15H
SRONXYPFSAKOGH-UHFFFAOYSA-N
MFCD00039424
E3TNT8VK8L
SCHEMBL62295
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclopentadecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 + 0.7960 79.60%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.4916 49.16%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.9859 98.59%
OATP1B3 inhibitior + 0.9628 96.28%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8692 86.92%
P-glycoprotein inhibitior - 0.9717 97.17%
P-glycoprotein substrate - 0.9977 99.77%
CYP3A4 substrate - 0.8678 86.78%
CYP2C9 substrate - 0.7696 76.96%
CYP2D6 substrate - 0.7147 71.47%
CYP3A4 inhibition - 0.9892 98.92%
CYP2C9 inhibition - 0.9330 93.30%
CYP2C19 inhibition - 0.9599 95.99%
CYP2D6 inhibition - 0.9724 97.24%
CYP1A2 inhibition - 0.8594 85.94%
CYP2C8 inhibition - 0.9974 99.74%
CYP inhibitory promiscuity - 0.8592 85.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Warning 0.4829 48.29%
Eye corrosion + 1.0000 100.00%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9136 91.36%
Skin corrosion - 0.7647 76.47%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5478 54.78%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8750 87.50%
skin sensitisation + 0.6221 62.21%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity - 0.9627 96.27%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5386 53.86%
Acute Oral Toxicity (c) IV 0.5022 50.22%
Estrogen receptor binding - 0.9427 94.27%
Androgen receptor binding - 0.9149 91.49%
Thyroid receptor binding - 0.8307 83.07%
Glucocorticoid receptor binding - 0.9259 92.59%
Aromatase binding - 0.8696 86.96%
PPAR gamma - 0.8975 89.75%
Honey bee toxicity - 0.8911 89.11%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.7700 77.00%

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
No predicted targets yet!

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.
Astilbe rubra

Cross-Links

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PubChem 67525
NPASS NPC10642