Chloroxanthin

Details

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Internal ID bc9ffd17-9a3f-486a-808a-1b1a0f936f84
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (6E,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,8,10,12,14,16,18,20,22,26,30-undecaen-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H60O/c1-33(2)19-13-22-36(5)25-16-28-37(6)26-14-23-34(3)20-11-12-21-35(4)24-15-27-38(7)29-17-30-39(8)31-18-32-40(9,10)41/h11-12,14-15,17,19-21,23-27,29-30,41H,13,16,18,22,28,31-32H2,1-10H3/b12-11+,23-14+,24-15+,29-17+,34-20+,35-21+,36-25+,37-26+,38-27+,39-30+
InChI Key IWZRTQIXVDXLNL-PZKADDIDSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C40H60O
Molecular Weight 556.90 g/mol
Exact Mass 556.464416533 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 14.20
Atomic LogP (AlogP) 12.36
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 18

Synonyms

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Hydroxyneurosporene
2104-74-7
Chloroxanthin/ Hydroxyneurosporene/ OH-Neurosporene
OH-Neurosporene
SCHEMBL2832876
CHEBI:80158
CHEBI:138077
DTXSID601315591
LMPR01070113
1-hydroxy-all-trans-1,2-dihydroneurosporene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Chloroxanthin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 - 0.7738 77.38%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.3611 36.11%
OATP2B1 inhibitior - 0.5730 57.30%
OATP1B1 inhibitior + 0.8618 86.18%
OATP1B3 inhibitior + 0.9609 96.09%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9967 99.67%
P-glycoprotein inhibitior + 0.7997 79.97%
P-glycoprotein substrate - 0.7776 77.76%
CYP3A4 substrate + 0.5649 56.49%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7761 77.61%
CYP3A4 inhibition - 0.9100 91.00%
CYP2C9 inhibition - 0.7941 79.41%
CYP2C19 inhibition - 0.8107 81.07%
CYP2D6 inhibition - 0.9470 94.70%
CYP1A2 inhibition - 0.6520 65.20%
CYP2C8 inhibition - 0.8375 83.75%
CYP inhibitory promiscuity - 0.7646 76.46%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6452 64.52%
Eye corrosion - 0.8146 81.46%
Eye irritation - 0.9045 90.45%
Skin irritation + 0.7659 76.59%
Skin corrosion - 0.9749 97.49%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9454 94.54%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.8176 81.76%
skin sensitisation + 0.8780 87.80%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8053 80.53%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6123 61.23%
Acute Oral Toxicity (c) III 0.7571 75.71%
Estrogen receptor binding + 0.8269 82.69%
Androgen receptor binding + 0.5486 54.86%
Thyroid receptor binding + 0.7533 75.33%
Glucocorticoid receptor binding + 0.5623 56.23%
Aromatase binding - 0.6578 65.78%
PPAR gamma + 0.7511 75.11%
Honey bee toxicity - 0.8725 87.25%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.8940 89.40%

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 96.15% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.09% 91.11%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 87.93% 87.16%
CHEMBL3401 O75469 Pregnane X receptor 87.43% 94.73%
CHEMBL2581 P07339 Cathepsin D 87.40% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.10% 96.09%
CHEMBL1977 P11473 Vitamin D receptor 85.28% 99.43%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.88% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.20% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.67% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.99% 97.25%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.99% 89.34%
CHEMBL2061 P19793 Retinoid X receptor alpha 80.01% 91.67%

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.
There are no matching plants.

Cross-Links

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PubChem 9915740
LOTUS LTS0092142
wikiData Q27149272