Cyclotetracosane

Details

Top
Internal ID 070832ed-e5f8-4cfb-a946-f1af4f7a8250
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name cyclotetracosane
SMILES (Canonical) C1CCCCCCCCCCCCCCCCCCCCCCC1
SMILES (Isomeric) C1CCCCCCCCCCCCCCCCCCCCCCC1
InChI InChI=1S/C24H48/c1-2-4-6-8-10-12-14-16-18-20-22-24-23-21-19-17-15-13-11-9-7-5-3-1/h1-24H2
InChI Key OOTMSKDHDITFHF-UHFFFAOYSA-N
Popularity 29 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H48
Molecular Weight 336.60 g/mol
Exact Mass 336.375601531 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 13.00
Atomic LogP (AlogP) 9.36
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
297-03-0
DTXSID20334354
OOTMSKDHDITFHF-UHFFFAOYSA-N

2D Structure

Top
2D Structure of Cyclotetracosane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 + 0.7599 75.99%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.4916 49.16%
OATP2B1 inhibitior - 0.8598 85.98%
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 - 0.7936 79.36%
P-glycoprotein inhibitior - 0.9505 95.05%
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 - 0.4907 49.07%
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 - 0.8396 83.96%
Androgen receptor binding - 0.9149 91.49%
Thyroid receptor binding - 0.8199 81.99%
Glucocorticoid receptor binding - 0.8873 88.73%
Aromatase binding - 0.8035 80.35%
PPAR gamma - 0.8317 83.17%
Honey bee toxicity - 0.8911 89.11%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.7700 77.00%

Targets

Top

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

Top
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.
Empetrum nigrum
Wurfbainia longiligularis
Wurfbainia villosa
Wurfbainia villosa var. xanthioides

Cross-Links

Top
PubChem 520449
NPASS NPC139337
LOTUS LTS0018080
wikiData Q81985682