Tricosane

Details

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Internal ID e94e6a5d-6027-48c7-ac7c-b765e5f35dc5
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name tricosane
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCCCCC
InChI InChI=1S/C23H48/c1-3-5-7-9-11-13-15-17-19-21-23-22-20-18-16-14-12-10-8-6-4-2/h3-23H2,1-2H3
InChI Key FIGVVZUWCLSUEI-UHFFFAOYSA-N
Popularity 939 references in papers

Physical and Chemical Properties

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Molecular Formula C23H48
Molecular Weight 324.60 g/mol
Exact Mass 324.375601531 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 12.10
Atomic LogP (AlogP) 9.22
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 20

Synonyms

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n-Tricosane
638-67-5
Docosane, methyl-
Tricosan
UNII-T166B8R1VC
T166B8R1VC
EINECS 211-347-4
NSC 78487
NSC-78487
AI3-35917
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Tricosane

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 + 0.8385 83.85%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5981 59.81%
OATP2B1 inhibitior - 0.8500 85.00%
OATP1B1 inhibitior + 0.9552 95.52%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7181 71.81%
P-glycoprotein inhibitior - 0.8539 85.39%
P-glycoprotein substrate - 0.9516 95.16%
CYP3A4 substrate - 0.7947 79.47%
CYP2C9 substrate - 0.8415 84.15%
CYP2D6 substrate - 0.7215 72.15%
CYP3A4 inhibition - 0.9877 98.77%
CYP2C9 inhibition - 0.9349 93.49%
CYP2C19 inhibition - 0.9540 95.40%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.6175 61.75%
CYP2C8 inhibition - 0.9765 97.65%
CYP inhibitory promiscuity - 0.8149 81.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6328 63.28%
Eye corrosion + 0.9946 99.46%
Eye irritation + 0.9856 98.56%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.9874 98.74%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8288 82.88%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8836 88.36%
skin sensitisation + 0.9563 95.63%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.6948 69.48%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6552 65.52%
Acute Oral Toxicity (c) III 0.6143 61.43%
Estrogen receptor binding - 0.7013 70.13%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.7242 72.42%
Glucocorticoid receptor binding - 0.8785 87.85%
Aromatase binding - 0.6310 63.10%
PPAR gamma - 0.7437 74.37%
Honey bee toxicity - 0.9939 99.39%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity + 0.8690 86.90%
Fish aquatic toxicity + 0.9770 97.70%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.23% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.92% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 91.78% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.44% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.64% 91.81%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.59% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.93% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.52% 87.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.15% 85.94%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 83.58% 90.24%
CHEMBL2996 Q05655 Protein kinase C delta 83.44% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.77% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 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.
Abies sachalinensis
Abutilon indicum
Actaea cimicifuga
Actaea dahurica
Actaea simplex
Agave decipiens
Allium ampeloprasum
Annona squamosa
Anthemis aciphylla
Aquilaria malaccensis
Aquilaria sinensis
Arabidopsis thaliana
Armoracia rusticana
Arnica montana
Artemisia annua
Artemisia argyi
Artemisia capillaris
Artemisia montana
Artemisia princeps
Betula pubescens var. litwinowii
Cannabis sativa
Castanopsis cuspidata
Cestrum nocturnum
Chrysanthemum indicum
Cistus creticus
Cistus monspeliensis
Citrus × aurantium
Crocus sativus
Cupressus nootkatensis
Cynomorium coccineum subsp. songaricum
Dactylanthus taylorii
Daphne odora
Digitalis purpurea
Echinacea angustifolia
Endopappus macrocarpus subsp. macrocarpus
Ephedra sinica
Euphorbia lactiflua
Foeniculum vulgare
Ginkgo biloba
Glebionis coronaria
Glycyrrhiza uralensis
Hamamelis virginiana
Hypericum perforatum
Laggera crispata
Lilium pumilum
Lycium chinense
Manilkara bidentata
Mitracarpus hirtus
Morina persica
Nelumbo lutea
Panax ginseng
Pelargonium endlicherianum
Persicaria bistorta
Plantago ovata
Plumeria rubra
Populus alba
Primula latifolia
Prunus laurocerasus
Prunus persica
Pseudowintera colorata
Rosa gallica
Rosa multiflora
Salvia fruticosa
Scutellaria baicalensis
Senecio cerberoanus
Senna alexandrina
Sesbania grandiflora
Sideritis hispida
Sideritis taurica
Spathiphyllum cannifolium
Symphytum tuberosum
Tanacetum cinerariifolium
Tilia platyphyllos
Tripleurospermum inodorum
Vanilla planifolia
Vincetoxicum glaucescens
Vincetoxicum stauntonii
Viscum album
Viscum coloratum
Vitis vinifera
Zinnia elegans

Cross-Links

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PubChem 12534
NPASS NPC278683
LOTUS LTS0089836
wikiData Q150977