Mollicellin Q

Details

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Internal ID bb251be2-6523-4475-9768-b2f54ebcc54a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 11-(ethoxymethyl)-3,10-dihydroxy-2,2,5,8-tetramethyl-3,4-dihydrochromeno[7,6-b][1,4]benzodioxepin-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H26O7/c1-6-27-10-14-15(24)7-11(2)19-21(14)28-17-9-16-13(8-18(25)23(4,5)30-16)12(3)20(17)29-22(19)26/h7,9,18,24-25H,6,8,10H2,1-5H3
InChI Key RCLMCNQLMYPAFZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H26O7
Molecular Weight 414.40 g/mol
Exact Mass 414.16785316 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.94
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Mollicellin Q

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9804 98.04%
Caco-2 + 0.6832 68.32%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6172 61.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7917 79.17%
OATP1B3 inhibitior + 0.8837 88.37%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9091 90.91%
P-glycoprotein inhibitior - 0.5138 51.38%
P-glycoprotein substrate - 0.7369 73.69%
CYP3A4 substrate + 0.6600 66.00%
CYP2C9 substrate - 0.5815 58.15%
CYP2D6 substrate - 0.8000 80.00%
CYP3A4 inhibition - 0.9675 96.75%
CYP2C9 inhibition - 0.8485 84.85%
CYP2C19 inhibition - 0.7852 78.52%
CYP2D6 inhibition - 0.9238 92.38%
CYP1A2 inhibition - 0.6495 64.95%
CYP2C8 inhibition + 0.7811 78.11%
CYP inhibitory promiscuity - 0.9270 92.70%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6496 64.96%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.7012 70.12%
Skin irritation - 0.8258 82.58%
Skin corrosion - 0.9525 95.25%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4539 45.39%
Micronuclear - 0.5967 59.67%
Hepatotoxicity - 0.5892 58.92%
skin sensitisation - 0.8243 82.43%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6173 61.73%
Acute Oral Toxicity (c) III 0.6464 64.64%
Estrogen receptor binding + 0.9384 93.84%
Androgen receptor binding + 0.6459 64.59%
Thyroid receptor binding + 0.7052 70.52%
Glucocorticoid receptor binding + 0.9095 90.95%
Aromatase binding + 0.8207 82.07%
PPAR gamma + 0.8263 82.63%
Honey bee toxicity - 0.8312 83.12%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9395 93.95%

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 99.32% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.53% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.98% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.53% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.60% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 90.36% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.41% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 89.13% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.08% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.22% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.93% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.51% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.14% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.66% 96.09%
CHEMBL4208 P20618 Proteasome component C5 81.68% 90.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.52% 94.80%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.04% 100.00%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 80.79% 96.37%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.01% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.00% 82.38%

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.
There are no matching plants.

Cross-Links

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PubChem 146684102
LOTUS LTS0253683
wikiData Q105233757