Mitissimol D

Details

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Internal ID b551de06-198c-401f-a942-299d487fd4be
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 3,10-dihydroxy-1,5,9,9-tetramethyl-12-oxabicyclo[9.1.0]dodeca-4,7-dien-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O4/c1-9-7-10(16)8-15(4)13(19-15)12(18)14(2,3)6-5-11(9)17/h5-7,10,12-13,16,18H,8H2,1-4H3
InChI Key WNPDAXBIZXDZEZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O4
Molecular Weight 266.33 g/mol
Exact Mass 266.15180918 g/mol
Topological Polar Surface Area (TPSA) 70.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.37
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Mitissimol D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9754 97.54%
Caco-2 + 0.5369 53.69%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.4780 47.80%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.9358 93.58%
OATP1B3 inhibitior + 0.9712 97.12%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9130 91.30%
P-glycoprotein inhibitior - 0.9417 94.17%
P-glycoprotein substrate - 0.8939 89.39%
CYP3A4 substrate + 0.5919 59.19%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.8651 86.51%
CYP3A4 inhibition - 0.7854 78.54%
CYP2C9 inhibition - 0.8195 81.95%
CYP2C19 inhibition - 0.6983 69.83%
CYP2D6 inhibition - 0.9125 91.25%
CYP1A2 inhibition - 0.7209 72.09%
CYP2C8 inhibition - 0.9483 94.83%
CYP inhibitory promiscuity - 0.8763 87.63%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4637 46.37%
Eye corrosion - 0.9791 97.91%
Eye irritation - 0.7965 79.65%
Skin irritation - 0.5753 57.53%
Skin corrosion - 0.8999 89.99%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7128 71.28%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5467 54.67%
skin sensitisation - 0.5607 56.07%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.6206 62.06%
Acute Oral Toxicity (c) III 0.4677 46.77%
Estrogen receptor binding - 0.5857 58.57%
Androgen receptor binding - 0.6337 63.37%
Thyroid receptor binding - 0.4931 49.31%
Glucocorticoid receptor binding - 0.5217 52.17%
Aromatase binding - 0.6259 62.59%
PPAR gamma - 0.6938 69.38%
Honey bee toxicity - 0.9044 90.44%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.6690 66.90%

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 89.83% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.55% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.95% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.53% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.92% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.66% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.35% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.23% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.61% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.93% 85.14%

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 73231462
LOTUS LTS0275955
wikiData Q75067568