(3S,6E,10E,15S,19S,23S,27S,31S)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-1,6,10,34-tetraene-3,15,19,23,27,31-hexol

Details

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Internal ID bc544c29-4f81-4f54-a1f9-9b08cf9bb388
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Polyterpenoids
IUPAC Name (3S,6E,10E,15S,19S,23S,27S,31S)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-1,6,10,34-tetraene-3,15,19,23,27,31-hexol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C45H84O6/c1-12-40(6,46)26-15-24-38(4)22-13-23-39(5)25-16-28-42(8,48)30-18-32-44(10,50)34-20-36-45(11,51)35-19-33-43(9,49)31-17-29-41(7,47)27-14-21-37(2)3/h12,21,23-24,46-51H,1,13-20,22,25-36H2,2-11H3/b38-24+,39-23+/t40-,41-,42+,43-,44+,45-/m1/s1
InChI Key DGMDXWIMXBSSCY-SZJXBIQWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C45H84O6
Molecular Weight 721.10 g/mol
Exact Mass 720.62679039 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 9.60
Atomic LogP (AlogP) 10.73
H-Bond Acceptor 6
H-Bond Donor 6
Rotatable Bonds 30

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,6E,10E,15S,19S,23S,27S,31S)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-1,6,10,34-tetraene-3,15,19,23,27,31-hexol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9656 96.56%
Caco-2 - 0.8337 83.37%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5316 53.16%
OATP2B1 inhibitior - 0.5695 56.95%
OATP1B1 inhibitior + 0.9117 91.17%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8721 87.21%
P-glycoprotein inhibitior + 0.6895 68.95%
P-glycoprotein substrate - 0.8515 85.15%
CYP3A4 substrate + 0.5477 54.77%
CYP2C9 substrate - 0.7899 78.99%
CYP2D6 substrate - 0.7511 75.11%
CYP3A4 inhibition - 0.7651 76.51%
CYP2C9 inhibition - 0.8277 82.77%
CYP2C19 inhibition - 0.8128 81.28%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.7661 76.61%
CYP2C8 inhibition - 0.7711 77.11%
CYP inhibitory promiscuity - 0.8303 83.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.7290 72.90%
Eye corrosion - 0.9213 92.13%
Eye irritation - 0.8820 88.20%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9814 98.14%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4630 46.30%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6924 69.24%
skin sensitisation + 0.6894 68.94%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.7941 79.41%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.4553 45.53%
Acute Oral Toxicity (c) III 0.7594 75.94%
Estrogen receptor binding + 0.7148 71.48%
Androgen receptor binding - 0.5718 57.18%
Thyroid receptor binding + 0.5417 54.17%
Glucocorticoid receptor binding + 0.5885 58.85%
Aromatase binding + 0.5879 58.79%
PPAR gamma + 0.6924 69.24%
Honey bee toxicity - 0.8153 81.53%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9684 96.84%

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 96.37% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 92.28% 94.73%
CHEMBL2581 P07339 Cathepsin D 90.19% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.62% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.12% 96.95%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.40% 90.93%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 83.15% 96.90%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.92% 96.09%

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 162989687
LOTUS LTS0068013
wikiData Q104978899