Erythroxydiol X

Details

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Internal ID bae2d9ee-9350-479e-80f0-3e5bdbd016ab
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1R)-1-[(1S,4S,6S,9S,10R,14S)-6,9,14-trimethyl-6-tetracyclo[8.5.0.01,14.04,9]pentadecanyl]ethane-1,2-diol
SMILES (Canonical) CC1(CCC2(C(C1)CCC34C2CCCC3(C4)C)C)C(CO)O
SMILES (Isomeric) C[C@@]1(CC[C@]2([C@H](C1)CC[C@]34[C@@H]2CCC[C@]3(C4)C)C)[C@H](CO)O
InChI InChI=1S/C20H34O2/c1-17(16(22)12-21)9-10-19(3)14(11-17)6-8-20-13-18(20,2)7-4-5-15(19)20/h14-16,21-22H,4-13H2,1-3H3/t14-,15+,16-,17-,18-,19-,20-/m0/s1
InChI Key JUZKDQHWDRIUAM-DTMQFJJTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O2
Molecular Weight 306.50 g/mol
Exact Mass 306.255880323 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.14
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Erythroxydiol X

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 + 0.5892 58.92%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.5449 54.49%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.8795 87.95%
OATP1B3 inhibitior + 0.9238 92.38%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8497 84.97%
P-glycoprotein inhibitior - 0.9158 91.58%
P-glycoprotein substrate - 0.7977 79.77%
CYP3A4 substrate + 0.5891 58.91%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.7213 72.13%
CYP3A4 inhibition - 0.7144 71.44%
CYP2C9 inhibition - 0.5781 57.81%
CYP2C19 inhibition - 0.7025 70.25%
CYP2D6 inhibition - 0.9137 91.37%
CYP1A2 inhibition - 0.5342 53.42%
CYP2C8 inhibition - 0.8227 82.27%
CYP inhibitory promiscuity - 0.8805 88.05%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.7356 73.56%
Eye corrosion - 0.9678 96.78%
Eye irritation - 0.8051 80.51%
Skin irritation - 0.7746 77.46%
Skin corrosion - 0.9675 96.75%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6422 64.22%
skin sensitisation - 0.6094 60.94%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.7638 76.38%
Acute Oral Toxicity (c) III 0.6938 69.38%
Estrogen receptor binding + 0.8597 85.97%
Androgen receptor binding + 0.5396 53.96%
Thyroid receptor binding + 0.7079 70.79%
Glucocorticoid receptor binding + 0.7940 79.40%
Aromatase binding + 0.6915 69.15%
PPAR gamma - 0.5971 59.71%
Honey bee toxicity - 0.8887 88.87%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7816 78.16%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.77% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.36% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.99% 97.09%
CHEMBL206 P03372 Estrogen receptor alpha 93.41% 97.64%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.69% 91.11%
CHEMBL237 P41145 Kappa opioid receptor 89.60% 98.10%
CHEMBL2581 P07339 Cathepsin D 87.04% 98.95%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 85.87% 96.38%
CHEMBL259 P32245 Melanocortin receptor 4 85.45% 95.38%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.56% 100.00%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 84.54% 95.58%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.52% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.18% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.89% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.67% 95.50%
CHEMBL4198 P98170 Inhibitor of apoptosis protein 3 83.12% 97.79%
CHEMBL2094135 Q96BI3 Gamma-secretase 81.49% 98.05%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 80.53% 99.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.46% 97.14%
CHEMBL221 P23219 Cyclooxygenase-1 80.43% 90.17%

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.
Erythroxylum barbatum

Cross-Links

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PubChem 15559160
LOTUS LTS0020475
wikiData Q104402204