(6E,11R,14E,18E)-2,6,15,19,23-pentamethyl-10-methylidenetetracosa-2,6,14,18,22-pentaen-11-ol

Details

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Internal ID d6b1a331-a71e-40f5-81af-fe569525e7f1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (6E,11R,14E,18E)-2,6,15,19,23-pentamethyl-10-methylidenetetracosa-2,6,14,18,22-pentaen-11-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H50O/c1-24(2)14-9-16-26(5)18-11-19-28(7)21-13-23-30(31)29(8)22-12-20-27(6)17-10-15-25(3)4/h14-15,18,20-21,30-31H,8-13,16-17,19,22-23H2,1-7H3/b26-18+,27-20+,28-21+/t30-/m1/s1
InChI Key MUINNOMLJWUSBP-KLMKBRDJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O
Molecular Weight 426.70 g/mol
Exact Mass 426.386166214 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 10.60
Atomic LogP (AlogP) 9.58
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6E,11R,14E,18E)-2,6,15,19,23-pentamethyl-10-methylidenetetracosa-2,6,14,18,22-pentaen-11-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 - 0.5619 56.19%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.3443 34.43%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9430 94.30%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8951 89.51%
P-glycoprotein inhibitior + 0.5786 57.86%
P-glycoprotein substrate - 0.9053 90.53%
CYP3A4 substrate - 0.5721 57.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6917 69.17%
CYP3A4 inhibition - 0.8697 86.97%
CYP2C9 inhibition - 0.8607 86.07%
CYP2C19 inhibition - 0.8506 85.06%
CYP2D6 inhibition - 0.9420 94.20%
CYP1A2 inhibition - 0.6641 66.41%
CYP2C8 inhibition - 0.9580 95.80%
CYP inhibitory promiscuity - 0.7844 78.44%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6899 68.99%
Eye corrosion - 0.6868 68.68%
Eye irritation - 0.7692 76.92%
Skin irritation + 0.6503 65.03%
Skin corrosion - 0.9720 97.20%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4197 41.97%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6912 69.12%
skin sensitisation + 0.8749 87.49%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.8919 89.19%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6414 64.14%
Acute Oral Toxicity (c) III 0.7525 75.25%
Estrogen receptor binding - 0.4797 47.97%
Androgen receptor binding - 0.7348 73.48%
Thyroid receptor binding + 0.5971 59.71%
Glucocorticoid receptor binding + 0.5646 56.46%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7231 72.31%
Honey bee toxicity - 0.8122 81.22%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9541 95.41%

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 94.40% 92.08%
CHEMBL2581 P07339 Cathepsin D 91.11% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.72% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.00% 91.11%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.02% 93.10%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.72% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 81.28% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.70% 99.17%

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.
Croton hieronymi

Cross-Links

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PubChem 162989231
LOTUS LTS0106517
wikiData Q105172408