Erythrodiene

Details

Top
Internal ID eb7255f8-ec71-4b59-b02d-dd298ed0ef09
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (7S)-4,10-dimethylidene-7-propan-2-ylspiro[4.5]decane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-11(2)14-8-7-13(4)15(10-14)9-5-6-12(15)3/h11,14H,3-10H2,1-2H3/t14-,15?/m0/s1
InChI Key WKUVNTPZIMJKBY-MLCCFXAWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
WKUVNTPZIMJKBY-MLCCFXAWSA-N

2D Structure

Top
2D Structure of Erythrodiene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.8284 82.84%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.8183 81.83%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9485 94.85%
OATP1B3 inhibitior + 0.8990 89.90%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8585 85.85%
P-glycoprotein inhibitior - 0.9246 92.46%
P-glycoprotein substrate - 0.8975 89.75%
CYP3A4 substrate - 0.5440 54.40%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.7620 76.20%
CYP3A4 inhibition - 0.9311 93.11%
CYP2C9 inhibition - 0.8455 84.55%
CYP2C19 inhibition - 0.7827 78.27%
CYP2D6 inhibition - 0.9357 93.57%
CYP1A2 inhibition - 0.8111 81.11%
CYP2C8 inhibition - 0.9416 94.16%
CYP inhibitory promiscuity - 0.8016 80.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Warning 0.4636 46.36%
Eye corrosion - 0.7164 71.64%
Eye irritation + 0.9132 91.32%
Skin irritation + 0.5272 52.72%
Skin corrosion - 0.9893 98.93%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5940 59.40%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5605 56.05%
skin sensitisation + 0.8991 89.91%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.6289 62.89%
Nephrotoxicity + 0.5606 56.06%
Acute Oral Toxicity (c) III 0.7645 76.45%
Estrogen receptor binding - 0.8561 85.61%
Androgen receptor binding - 0.7301 73.01%
Thyroid receptor binding - 0.7085 70.85%
Glucocorticoid receptor binding - 0.6686 66.86%
Aromatase binding - 0.8525 85.25%
PPAR gamma - 0.7328 73.28%
Honey bee toxicity - 0.8690 86.90%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9969 99.69%

Targets

Top

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
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 94.94% 96.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.81% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.49% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.22% 95.89%
CHEMBL5203 P33316 dUTP pyrophosphatase 86.74% 99.18%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.05% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.35% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.47% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.14% 91.11%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.01% 93.04%
CHEMBL2007625 O75874 Isocitrate dehydrogenase [NADP] cytoplasmic 80.24% 99.00%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 91750188
LOTUS LTS0237454
wikiData Q105307720