(2R,3S,5E,7S,8Z)-4-chloro-3,7-dihydroxy-2-methyl-2,3,4,7-tetrahydrooxecin-10-one

Details

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Internal ID 6af0df97-f9cd-40a9-be42-26574f15e78d
Taxonomy Organoheterocyclic compounds > Oxocins
IUPAC Name (2R,3S,5E,7S,8Z)-4-chloro-3,7-dihydroxy-2-methyl-2,3,4,7-tetrahydrooxecin-10-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H13ClO4/c1-6-10(14)8(11)4-2-7(12)3-5-9(13)15-6/h2-8,10,12,14H,1H3/b4-2+,5-3-/t6-,7-,8?,10+/m1/s1
InChI Key IIIFVUMJBALUGH-NMTNZHRMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H13ClO4
Molecular Weight 232.66 g/mol
Exact Mass 232.0502366 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.37
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 (2R,3S,5E,7S,8Z)-4-chloro-3,7-dihydroxy-2-methyl-2,3,4,7-tetrahydrooxecin-10-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9728 97.28%
Caco-2 + 0.6420 64.20%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6691 66.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8606 86.06%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9565 95.65%
P-glycoprotein inhibitior - 0.9722 97.22%
P-glycoprotein substrate - 0.9578 95.78%
CYP3A4 substrate - 0.5788 57.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8928 89.28%
CYP3A4 inhibition - 0.9195 91.95%
CYP2C9 inhibition - 0.8541 85.41%
CYP2C19 inhibition - 0.8234 82.34%
CYP2D6 inhibition - 0.9032 90.32%
CYP1A2 inhibition - 0.8614 86.14%
CYP2C8 inhibition - 0.9732 97.32%
CYP inhibitory promiscuity - 0.9048 90.48%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.7367 73.67%
Carcinogenicity (trinary) Danger 0.5571 55.71%
Eye corrosion - 0.7660 76.60%
Eye irritation - 0.8008 80.08%
Skin irritation + 0.5493 54.93%
Skin corrosion - 0.6977 69.77%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7876 78.76%
Micronuclear + 0.6201 62.01%
Hepatotoxicity + 0.6303 63.03%
skin sensitisation - 0.6909 69.09%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5766 57.66%
Acute Oral Toxicity (c) III 0.6241 62.41%
Estrogen receptor binding - 0.7860 78.60%
Androgen receptor binding - 0.8370 83.70%
Thyroid receptor binding - 0.6420 64.20%
Glucocorticoid receptor binding - 0.5612 56.12%
Aromatase binding - 0.8801 88.01%
PPAR gamma - 0.7542 75.42%
Honey bee toxicity - 0.8296 82.96%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.8602 86.02%

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 92.19% 87.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.84% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.47% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.46% 81.11%
CHEMBL3401 O75469 Pregnane X receptor 86.64% 94.73%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.31% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.97% 86.33%

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 25111598
LOTUS LTS0251787
wikiData Q105113507