(4S,5R,6S)-6-chloro-4,5-dihydroxy-3-methoxycyclohex-2-en-1-one

Details

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Internal ID 23834510-cf79-4508-a26e-158b95555aba
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name (4S,5R,6S)-6-chloro-4,5-dihydroxy-3-methoxycyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9ClO4/c1-12-4-2-3(9)5(8)7(11)6(4)10/h2,5-7,10-11H,1H3/t5-,6-,7+/m1/s1
InChI Key QSEIAQVQXUHJCV-QYNIQEEDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9ClO4
Molecular Weight 192.60 g/mol
Exact Mass 192.0189365 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP -0.80
Atomic LogP (AlogP) -0.57
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4S,5R,6S)-6-chloro-4,5-dihydroxy-3-methoxycyclohex-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9705 97.05%
Caco-2 - 0.6058 60.58%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8470 84.70%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9235 92.35%
OATP1B3 inhibitior + 0.9677 96.77%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9153 91.53%
P-glycoprotein inhibitior - 0.9380 93.80%
P-glycoprotein substrate - 0.9516 95.16%
CYP3A4 substrate - 0.5708 57.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8524 85.24%
CYP3A4 inhibition - 0.9123 91.23%
CYP2C9 inhibition - 0.8017 80.17%
CYP2C19 inhibition - 0.5855 58.55%
CYP2D6 inhibition - 0.8740 87.40%
CYP1A2 inhibition - 0.6053 60.53%
CYP2C8 inhibition - 0.9495 94.95%
CYP inhibitory promiscuity - 0.8018 80.18%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6566 65.66%
Carcinogenicity (trinary) Non-required 0.4522 45.22%
Eye corrosion - 0.8626 86.26%
Eye irritation - 0.6561 65.61%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.8314 83.14%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8164 81.64%
Micronuclear + 0.5733 57.33%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.5784 57.84%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5979 59.79%
Acute Oral Toxicity (c) III 0.5719 57.19%
Estrogen receptor binding + 0.5323 53.23%
Androgen receptor binding - 0.6948 69.48%
Thyroid receptor binding - 0.5966 59.66%
Glucocorticoid receptor binding - 0.6884 68.84%
Aromatase binding - 0.8273 82.73%
PPAR gamma + 0.5222 52.22%
Honey bee toxicity - 0.7531 75.31%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9083 90.83%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.59% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.93% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 88.36% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.85% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.60% 94.45%
CHEMBL2581 P07339 Cathepsin D 85.53% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.63% 94.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 130894917
LOTUS LTS0005433
wikiData Q105226895