2,31-Dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene-3,30-dione

Details

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Internal ID b76a1ee4-66b2-47e8-a1ad-630217979368
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name 2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene-3,30-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H56O4/c1-33(21-15-23-35(3)25-17-27-37(5)29-31-39(43)41(7,8)45-11)19-13-14-20-34(2)22-16-24-36(4)26-18-28-38(6)30-32-40(44)42(9,10)46-12/h13-32H,1-12H3
InChI Key MNKGOUOMGDXWPK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C42H56O4
Molecular Weight 624.90 g/mol
Exact Mass 624.41786026 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 12.30
Atomic LogP (AlogP) 10.55
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 18

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,31-Dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene-3,30-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9754 97.54%
Caco-2 - 0.8129 81.29%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7954 79.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8816 88.16%
OATP1B3 inhibitior + 0.9582 95.82%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9897 98.97%
P-glycoprotein inhibitior + 0.8180 81.80%
P-glycoprotein substrate - 0.9355 93.55%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8583 85.83%
CYP3A4 inhibition - 0.8022 80.22%
CYP2C9 inhibition - 0.8254 82.54%
CYP2C19 inhibition - 0.7834 78.34%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition - 0.9097 90.97%
CYP2C8 inhibition - 0.9447 94.47%
CYP inhibitory promiscuity - 0.7483 74.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5107 51.07%
Carcinogenicity (trinary) Non-required 0.5865 58.65%
Eye corrosion - 0.6117 61.17%
Eye irritation - 0.8765 87.65%
Skin irritation - 0.6809 68.09%
Skin corrosion - 0.9837 98.37%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9243 92.43%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5435 54.35%
skin sensitisation + 0.8759 87.59%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.7721 77.21%
Acute Oral Toxicity (c) III 0.6054 60.54%
Estrogen receptor binding + 0.8159 81.59%
Androgen receptor binding - 0.5392 53.92%
Thyroid receptor binding + 0.7369 73.69%
Glucocorticoid receptor binding + 0.7452 74.52%
Aromatase binding + 0.5285 52.85%
PPAR gamma + 0.7386 73.86%
Honey bee toxicity - 0.7508 75.08%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.7246 72.46%

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
CHEMBL2581 P07339 Cathepsin D 86.24% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 85.35% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.12% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.55% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.89% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.36% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 80.06% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 552660
LOTUS LTS0041490
wikiData Q105168422