Spinulosin

Details

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Internal ID fe992772-50d1-459f-b0b2-9393e90bb271
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylquinones > Ubiquinones
IUPAC Name 2,5-dihydroxy-3-methoxy-6-methylcyclohexa-2,5-diene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H8O5/c1-3-4(9)6(11)8(13-2)7(12)5(3)10/h9,12H,1-2H3
InChI Key GFAZBXKENDSJEB-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O5
Molecular Weight 184.15 g/mol
Exact Mass 184.03717335 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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85-23-4
17WG1DAS77
2,5-dihydroxy-3-methoxy-6-methylcyclohexa-2,5-diene-1,4-dione
3,6-dihydroxy-5-methoxy-p-toluquinone
3,6-dihydroxy-4-methoxy-2,5-toluquinone
2,5-Cyclohexadiene-1,4-dione, 2,5-dihydroxy-3-methoxy-6-methyl-
UNII-17WG1DAS77
HYDROXYFUMIGATIN
SPINULOSIN [MI]
SCHEMBL33978
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Spinulosin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9661 96.61%
Caco-2 - 0.7623 76.23%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.8380 83.80%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.9421 94.21%
OATP1B3 inhibitior + 0.9692 96.92%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9157 91.57%
P-glycoprotein inhibitior - 0.9380 93.80%
P-glycoprotein substrate - 0.9828 98.28%
CYP3A4 substrate - 0.6237 62.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8806 88.06%
CYP3A4 inhibition - 0.9354 93.54%
CYP2C9 inhibition - 0.8242 82.42%
CYP2C19 inhibition - 0.6848 68.48%
CYP2D6 inhibition - 0.8217 82.17%
CYP1A2 inhibition - 0.8294 82.94%
CYP2C8 inhibition - 0.9790 97.90%
CYP inhibitory promiscuity - 0.8465 84.65%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7068 70.68%
Carcinogenicity (trinary) Non-required 0.6557 65.57%
Eye corrosion - 0.8819 88.19%
Eye irritation + 0.7969 79.69%
Skin irritation - 0.5449 54.49%
Skin corrosion - 0.9391 93.91%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7182 71.82%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5908 59.08%
skin sensitisation - 0.6034 60.34%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.7449 74.49%
Acute Oral Toxicity (c) III 0.4003 40.03%
Estrogen receptor binding - 0.7582 75.82%
Androgen receptor binding - 0.8242 82.42%
Thyroid receptor binding - 0.6892 68.92%
Glucocorticoid receptor binding - 0.7600 76.00%
Aromatase binding - 0.8056 80.56%
PPAR gamma - 0.8104 81.04%
Honey bee toxicity - 0.9112 91.12%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.8236 82.36%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.85% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.96% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.44% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.30% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 84.21% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.02% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.36% 94.00%

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.
There are no matching plants.

Cross-Links

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PubChem 66556
LOTUS LTS0159483
wikiData Q27251944