(4R,5R,6R)-4-hydroxy-2,3-dimethoxy-6-methyl-5-(3,7,11-trimethyldodeca-2,6,10-trienyl)cyclohex-2-en-1-one

Details

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Internal ID c4664001-da7a-46b0-a2e8-39a49c632241
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4R,5R,6R)-4-hydroxy-2,3-dimethoxy-6-methyl-5-(3,7,11-trimethyldodeca-2,6,10-trienyl)cyclohex-2-en-1-one
SMILES (Canonical) CC1C(C(C(=C(C1=O)OC)OC)O)CC=C(C)CCC=C(C)CCC=C(C)C
SMILES (Isomeric) C[C@@H]1[C@H]([C@H](C(=C(C1=O)OC)OC)O)CC=C(C)CCC=C(C)CCC=C(C)C
InChI InChI=1S/C24H38O4/c1-16(2)10-8-11-17(3)12-9-13-18(4)14-15-20-19(5)21(25)23(27-6)24(28-7)22(20)26/h10,12,14,19-20,22,26H,8-9,11,13,15H2,1-7H3/t19-,20-,22-/m1/s1
InChI Key LJTSIMVOOOLKOL-KCZVDYSFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H38O4
Molecular Weight 390.60 g/mol
Exact Mass 390.27700969 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.50
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R,5R,6R)-4-hydroxy-2,3-dimethoxy-6-methyl-5-(3,7,11-trimethyldodeca-2,6,10-trienyl)cyclohex-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.6916 69.16%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8563 85.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9002 90.02%
OATP1B3 inhibitior + 0.9291 92.91%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6314 63.14%
BSEP inhibitior + 0.8800 88.00%
P-glycoprotein inhibitior + 0.7415 74.15%
P-glycoprotein substrate - 0.8299 82.99%
CYP3A4 substrate + 0.5297 52.97%
CYP2C9 substrate - 0.7828 78.28%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.8102 81.02%
CYP2C9 inhibition - 0.7802 78.02%
CYP2C19 inhibition - 0.7091 70.91%
CYP2D6 inhibition - 0.8632 86.32%
CYP1A2 inhibition - 0.8280 82.80%
CYP2C8 inhibition - 0.8930 89.30%
CYP inhibitory promiscuity - 0.8743 87.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8314 83.14%
Carcinogenicity (trinary) Non-required 0.6895 68.95%
Eye corrosion - 0.9746 97.46%
Eye irritation - 0.9628 96.28%
Skin irritation - 0.6669 66.69%
Skin corrosion - 0.9794 97.94%
Ames mutagenesis - 0.6054 60.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7690 76.90%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5522 55.22%
skin sensitisation - 0.5957 59.57%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.5806 58.06%
Acute Oral Toxicity (c) III 0.6828 68.28%
Estrogen receptor binding - 0.5215 52.15%
Androgen receptor binding - 0.5410 54.10%
Thyroid receptor binding + 0.6643 66.43%
Glucocorticoid receptor binding + 0.6256 62.56%
Aromatase binding - 0.5965 59.65%
PPAR gamma + 0.5962 59.62%
Honey bee toxicity - 0.8042 80.42%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9852 98.52%

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
CHEMBL2581 P07339 Cathepsin D 94.59% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.05% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.32% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.32% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.78% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.11% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.59% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.79% 95.56%

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 155293261
LOTUS LTS0037001
wikiData Q105152790