2-(3,7,12,16,20,24-Hexamethylpentacosa-1,3,5,7,9,11,15,19,21,23-decaenyl)-1,3,3-trimethylcyclohexene

Details

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Internal ID bd035601-15ce-4ba6-bf0d-8bb495ccf2bd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Carotenes
IUPAC Name 2-(3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,15,19,21,23-decaenyl)-1,3,3-trimethylcyclohexene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H58/c1-32(2)18-13-21-35(5)24-15-26-36(6)25-14-22-33(3)19-11-12-20-34(4)23-16-27-37(7)29-30-39-38(8)28-17-31-40(39,9)10/h11-13,16,18-21,23-25,27,29-30H,14-15,17,22,26,28,31H2,1-10H3
InChI Key YRMTZGJDOCHJPY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C40H58
Molecular Weight 538.90 g/mol
Exact Mass 538.453851850 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 14.50
Atomic LogP (AlogP) 13.00
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3,7,12,16,20,24-Hexamethylpentacosa-1,3,5,7,9,11,15,19,21,23-decaenyl)-1,3,3-trimethylcyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 - 0.7387 73.87%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.5479 54.79%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior - 0.5604 56.04%
OATP1B3 inhibitior - 0.2942 29.42%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 1.0000 100.00%
P-glycoprotein inhibitior + 0.8693 86.93%
P-glycoprotein substrate - 0.7651 76.51%
CYP3A4 substrate + 0.6690 66.90%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.8896 88.96%
CYP2C9 inhibition - 0.8919 89.19%
CYP2C19 inhibition - 0.8956 89.56%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition - 0.8451 84.51%
CYP2C8 inhibition - 0.5978 59.78%
CYP inhibitory promiscuity - 0.5752 57.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Warning 0.4901 49.01%
Eye corrosion - 0.8210 82.10%
Eye irritation - 0.9049 90.49%
Skin irritation + 0.5691 56.91%
Skin corrosion - 0.9860 98.60%
Ames mutagenesis + 0.5631 56.31%
Human Ether-a-go-go-Related Gene inhibition + 0.9022 90.22%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5976 59.76%
skin sensitisation + 0.9289 92.89%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.7365 73.65%
Acute Oral Toxicity (c) III 0.7043 70.43%
Estrogen receptor binding + 0.8468 84.68%
Androgen receptor binding + 0.7018 70.18%
Thyroid receptor binding + 0.7552 75.52%
Glucocorticoid receptor binding + 0.5985 59.85%
Aromatase binding - 0.6482 64.82%
PPAR gamma + 0.7273 72.73%
Honey bee toxicity - 0.8569 85.69%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.54% 91.11%
CHEMBL2061 P19793 Retinoid X receptor alpha 94.11% 91.67%
CHEMBL1870 P28702 Retinoid X receptor beta 93.27% 95.00%
CHEMBL2004 P48443 Retinoid X receptor gamma 92.31% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.52% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.73% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.61% 95.50%
CHEMBL1937 Q92769 Histone deacetylase 2 88.89% 94.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.63% 91.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.16% 93.99%
CHEMBL2581 P07339 Cathepsin D 83.88% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.07% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.23% 95.56%

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.
Aloe arborescens

Cross-Links

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PubChem 162931205
LOTUS LTS0243875
wikiData Q105352899