Imicro,Imicro-Carotene, 2,2a(2)-bis(4-hydroxy-2-methyl-2-butenyl)-

Details

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Internal ID 24390f72-20d9-4980-b06f-0166402281a9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name 4-[5-[18-[5-(4-hydroxy-2-methylbut-2-enyl)-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-4,6,6-trimethylcyclohex-3-en-1-yl]-3-methylbut-2-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C50H72O2/c1-37(19-15-21-39(3)23-29-47-43(7)25-27-45(49(47,9)10)35-41(5)31-33-51)17-13-14-18-38(2)20-16-22-40(4)24-30-48-44(8)26-28-46(50(48,11)12)36-42(6)32-34-52/h13-26,29-32,45-48,51-52H,27-28,33-36H2,1-12H3
InChI Key BHONBYIDLOVJEW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C50H72O2
Molecular Weight 705.10 g/mol
Exact Mass 704.55323154 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 14.50
Atomic LogP (AlogP) 13.43
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 16

Synonyms

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epsilon,epsilon-Carotene, 2,2'-bis(4-hydroxy-2-methyl-2-butenyl)-
146285-20-3

2D Structure

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2D Structure of Imicro,Imicro-Carotene, 2,2a(2)-bis(4-hydroxy-2-methyl-2-butenyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9764 97.64%
Caco-2 - 0.8310 83.10%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.5112 51.12%
OATP2B1 inhibitior + 0.5724 57.24%
OATP1B1 inhibitior + 0.8419 84.19%
OATP1B3 inhibitior + 0.8550 85.50%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7343 73.43%
BSEP inhibitior + 0.9934 99.34%
P-glycoprotein inhibitior + 0.7876 78.76%
P-glycoprotein substrate - 0.6985 69.85%
CYP3A4 substrate + 0.5875 58.75%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8042 80.42%
CYP3A4 inhibition - 0.6725 67.25%
CYP2C9 inhibition - 0.7779 77.79%
CYP2C19 inhibition - 0.6390 63.90%
CYP2D6 inhibition - 0.8690 86.90%
CYP1A2 inhibition - 0.8221 82.21%
CYP2C8 inhibition - 0.6234 62.34%
CYP inhibitory promiscuity + 0.6706 67.06%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7241 72.41%
Carcinogenicity (trinary) Non-required 0.6108 61.08%
Eye corrosion - 0.9286 92.86%
Eye irritation - 0.9058 90.58%
Skin irritation - 0.6931 69.31%
Skin corrosion - 0.9302 93.02%
Ames mutagenesis - 0.6854 68.54%
Human Ether-a-go-go-Related Gene inhibition + 0.9508 95.08%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5697 56.97%
skin sensitisation - 0.5629 56.29%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5660 56.60%
Acute Oral Toxicity (c) III 0.7954 79.54%
Estrogen receptor binding + 0.8141 81.41%
Androgen receptor binding + 0.6794 67.94%
Thyroid receptor binding + 0.6734 67.34%
Glucocorticoid receptor binding + 0.7531 75.31%
Aromatase binding - 0.5094 50.94%
PPAR gamma + 0.7666 76.66%
Honey bee toxicity - 0.8899 88.99%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9882 98.82%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.57% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.53% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.42% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 84.91% 97.79%
CHEMBL2664 P23526 Adenosylhomocysteinase 84.87% 86.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.09% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.83% 97.09%
CHEMBL3524 P56524 Histone deacetylase 4 80.79% 92.97%

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 74052772
LOTUS LTS0101336
wikiData Q103816746