Pentacosane

Details

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Internal ID 50a1b154-7d14-4fcd-8ed2-8c56b0be613a
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name pentacosane
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCCCCCCC
InChI InChI=1S/C25H52/c1-3-5-7-9-11-13-15-17-19-21-23-25-24-22-20-18-16-14-12-10-8-6-4-2/h3-25H2,1-2H3
InChI Key YKNWIILGEFFOPE-UHFFFAOYSA-N
Popularity 884 references in papers

Physical and Chemical Properties

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Molecular Formula C25H52
Molecular Weight 352.70 g/mol
Exact Mass 352.406901659 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 13.10
Atomic LogP (AlogP) 10.00
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 22

Synonyms

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n-Pentacosane
629-99-2
UNII-BON9H94Y8V
BON9H94Y8V
EINECS 211-123-6
N-PENTACOSANE-D52
NSC 158663
NSC-158663
AI3-36478
DTXSID2060882
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pentacosane

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 + 0.7714 77.14%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5981 59.81%
OATP2B1 inhibitior - 0.8506 85.06%
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 - 0.6624 66.24%
P-glycoprotein inhibitior - 0.8393 83.93%
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 + 0.9871 98.71%
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 - 0.8194 81.94%
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 - 0.7050 70.50%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.6814 68.14%
Glucocorticoid receptor binding - 0.8562 85.62%
Aromatase binding - 0.5905 59.05%
PPAR gamma - 0.7061 70.61%
Honey bee toxicity - 0.9939 99.39%
Biodegradation + 0.9250 92.50%
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.
Abutilon indicum
Achillea arabica
Actaea cimicifuga
Actaea dahurica
Actaea simplex
Aegiceras corniculatum
Agave decipiens
Ajuga integrifolia
Allium ampeloprasum
Allium multibulbosum
Ampelopsis japonica
Angelica dahurica
Anthemis aciphylla
Aquilaria malaccensis
Aquilaria sinensis
Arbutus menziesii
Arctostaphylos patula
Arnica montana
Artemisia annua
Artemisia argyi
Artemisia montana
Artemisia princeps
Betula pendula
Bruguiera gymnorhiza
Cannabis sativa
Capparis decidua
Casearia ilicifolia
Castanopsis cuspidata
Centromadia fitchii
Cestrum nocturnum
Chrysanthemum indicum
Cinnamosma madagascariensis
Cistus albidus
Cistus creticus
Cistus monspeliensis
Citrus × aurantium
Citrus maxima
Clematis montana
Clerodendrum bungei
Clusia spiritu-sanctensis
Convolvulus arvensis
Crocus sativus
Cupressus nootkatensis
Cynomorium coccineum subsp. songaricum
Dactylanthus taylorii
Daphne odora
Digitalis purpurea
Diplotaxis harra
Echinacea angustifolia
Echiochilon pauciflorum
Euphorbia lactiflua
Euphorbia piscatoria
Festuca arundinacea
Ginkgo biloba
Glebionis coronaria
Hamamelis virginiana
Helichrysum ambiguum
Helichrysum nudifolium
Hypericum perforatum
Hypoxis nyasica
Isoberlinia angolensis
Ixora chinensis
Laggera crispata
Lilium pumilum
Lycopus lucidus
Lysimachia fordiana
Macaranga sinensis
Mandragora officinarum
Mangifera indica
Mirabilis jalapa
Morina persica
Nelumbo lutea
Nicoteba betonica
Origanum × adanense
Origanum vulgare
Otostegia fruticosa
Panax ginseng
Paranephelius uniflorus
Pelargonium endlicherianum
Persicaria bistorta
Phytolacca acinosa
Plantago major
Plantago ovata
Populus alba
Primula latifolia
Prunus laurocerasus
Prunus persica
Pseudowintera colorata
Rhododendron aureum
Rosa centifolia
Scutellaria baicalensis
Senna alexandrina
Seriphidium lessingianum
Sesbania grandiflora
Sonneratia alba
Spathiphyllum cannifolium
Tephroseris integrifolia
Terminalia tetraphylla
Teucrium orientale
Teucrium polium subsp. polium
Tilia platyphyllos
Tripleurospermum inodorum
Typha angustifolia
Typha domingensis
Vanilla madagascariensis
Veltheimia capensis
Vincetoxicum glaucescens
Vincetoxicum stauntonii
Viscum album
Viscum coloratum
Xylopia aethiopica
Zinnia elegans

Cross-Links

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PubChem 12406
NPASS NPC90232
LOTUS LTS0080764
wikiData Q151007