Asymmetrical zeta-carotene/Asym. zeta-carotene/7,8,11,12-Tetrahydrolycopene

Details

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Internal ID f4ab1f69-19d4-44a9-893f-672390ebf8e2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Carotenes
IUPAC Name (6E,8E,10E,12E,14E,16E,18E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,22,26,30-undecaene
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CC/C(=C/CC/C(=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C=C(\C)/CCC=C(C)C)/C)/C)/C)C
InChI InChI=1S/C40H60/c1-33(2)19-13-23-37(7)27-17-31-39(9)29-15-25-35(5)21-11-12-22-36(6)26-16-30-40(10)32-18-28-38(8)24-14-20-34(3)4/h11-12,15,17,19-22,25,27-31H,13-14,16,18,23-24,26,32H2,1-10H3/b12-11+,25-15+,31-17+,35-21+,36-22+,37-27+,38-28+,39-29+,40-30+
InChI Key YTZIWAULTIDEEY-JLGWONFISA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C40H60
Molecular Weight 540.90 g/mol
Exact Mass 540.469501914 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 15.50
Atomic LogP (AlogP) 13.39
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 18

Synonyms

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asym-zeta-Carotene
LMPR01070129
502-63-6

2D Structure

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2D Structure of Asymmetrical zeta-carotene/Asym. zeta-carotene/7,8,11,12-Tetrahydrolycopene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 - 0.7146 71.46%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Nucleus 0.6684 66.84%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8814 88.14%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9948 99.48%
P-glycoprotein inhibitior + 0.8443 84.43%
P-glycoprotein substrate - 0.9241 92.41%
CYP3A4 substrate - 0.5332 53.32%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7603 76.03%
CYP3A4 inhibition - 0.9716 97.16%
CYP2C9 inhibition - 0.9099 90.99%
CYP2C19 inhibition - 0.9168 91.68%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.7354 73.54%
CYP2C8 inhibition - 0.9408 94.08%
CYP inhibitory promiscuity - 0.6923 69.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4712 47.12%
Eye corrosion + 0.7181 71.81%
Eye irritation - 0.8931 89.31%
Skin irritation + 0.8835 88.35%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8910 89.10%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7676 76.76%
skin sensitisation + 0.9505 95.05%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.7180 71.80%
Acute Oral Toxicity (c) III 0.8971 89.71%
Estrogen receptor binding + 0.8448 84.48%
Androgen receptor binding - 0.5219 52.19%
Thyroid receptor binding + 0.7342 73.42%
Glucocorticoid receptor binding - 0.6168 61.68%
Aromatase binding - 0.6845 68.45%
PPAR gamma + 0.6918 69.18%
Honey bee toxicity - 0.8911 89.11%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9916 99.16%

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 95.40% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.95% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.33% 94.73%
CHEMBL2581 P07339 Cathepsin D 82.58% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.28% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 80.31% 90.17%

Cross-Links

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PubChem 16061252
NPASS NPC162050
LOTUS LTS0178208
wikiData Q105362448