Edulan I

Details

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Internal ID b0cb0ada-9cdd-4f74-a441-03e68837dfa2
Taxonomy Organoheterocyclic compounds > Benzopyrans
IUPAC Name 2,5,5,8a-tetramethyl-3,6-dihydro-2H-chromene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H20O/c1-10-6-7-11-12(2,3)8-5-9-13(11,4)14-10/h5,7,9-10H,6,8H2,1-4H3
InChI Key HUXGOQHTDHIKSS-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C13H20O
Molecular Weight 192.30 g/mol
Exact Mass 192.151415257 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.47
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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trans-Edulan
99881-86-4
2,5,5,8a-Tetramethyl-3,5,6,8a-tetrahydro-2H-chromene #
2,5,5,8a-tetramethyl-3,6-dihydro-2H-chromene
DTXSID90334543
CHEBI:184238
HUXGOQHTDHIKSS-UHFFFAOYSA-N
Q67879858
2,5,5,8a-tetramethyl-3,5,6,8a-tetrahydro-2H-1-benzopyran
3,5,6,8a-Tetrahydro-2,5,5,8a-tetramethyl-2H -1-benzopyran
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Edulan I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.8720 87.20%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4133 41.33%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.9073 90.73%
OATP1B3 inhibitior + 0.9617 96.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8196 81.96%
P-glycoprotein inhibitior - 0.9697 96.97%
P-glycoprotein substrate - 0.9205 92.05%
CYP3A4 substrate - 0.5316 53.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7393 73.93%
CYP3A4 inhibition - 0.7820 78.20%
CYP2C9 inhibition - 0.5410 54.10%
CYP2C19 inhibition + 0.6473 64.73%
CYP2D6 inhibition - 0.8960 89.60%
CYP1A2 inhibition - 0.6951 69.51%
CYP2C8 inhibition - 0.9079 90.79%
CYP inhibitory promiscuity - 0.5097 50.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.5189 51.89%
Eye corrosion - 0.9533 95.33%
Eye irritation + 0.6679 66.79%
Skin irritation - 0.6439 64.39%
Skin corrosion - 0.9521 95.21%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7108 71.08%
Micronuclear - 0.8399 83.99%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.7097 70.97%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5615 56.15%
Acute Oral Toxicity (c) III 0.7947 79.47%
Estrogen receptor binding - 0.9556 95.56%
Androgen receptor binding - 0.7003 70.03%
Thyroid receptor binding - 0.6452 64.52%
Glucocorticoid receptor binding - 0.9065 90.65%
Aromatase binding - 0.7912 79.12%
PPAR gamma - 0.8798 87.98%
Honey bee toxicity - 0.8997 89.97%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.8334 83.34%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.13% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.39% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.93% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.95% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 82.61% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.62% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.96% 99.23%
CHEMBL4040 P28482 MAP kinase ERK2 80.95% 83.82%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.72% 100.00%

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.
Chaenomeles speciosa

Cross-Links

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PubChem 521066
LOTUS LTS0124211
wikiData Q67879858