(2R,5S,7S)-3alpha-hydroxyexogonic acid

Details

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Internal ID b549b0eb-44b0-4479-971a-09c23ded5605
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name 2-[(2R,3R,5S,7S)-3-hydroxy-7-methyl-1,6-dioxaspiro[4.4]nonan-2-yl]acetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O5/c1-6-2-3-10(14-6)5-7(11)8(15-10)4-9(12)13/h6-8,11H,2-5H2,1H3,(H,12,13)/t6-,7+,8+,10-/m0/s1
InChI Key TZUFEMKJENBYIQ-WHQQTDPMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O5
Molecular Weight 216.23 g/mol
Exact Mass 216.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.51
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,5S,7S)-3alpha-hydroxyexogonic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8367 83.67%
Caco-2 - 0.6001 60.01%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7202 72.02%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.8991 89.91%
OATP1B3 inhibitior + 0.9173 91.73%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9496 94.96%
P-glycoprotein inhibitior - 0.9713 97.13%
P-glycoprotein substrate - 0.8956 89.56%
CYP3A4 substrate + 0.5397 53.97%
CYP2C9 substrate - 0.6023 60.23%
CYP2D6 substrate - 0.8730 87.30%
CYP3A4 inhibition - 0.8878 88.78%
CYP2C9 inhibition - 0.9330 93.30%
CYP2C19 inhibition - 0.8872 88.72%
CYP2D6 inhibition - 0.9667 96.67%
CYP1A2 inhibition - 0.8061 80.61%
CYP2C8 inhibition - 0.9503 95.03%
CYP inhibitory promiscuity - 0.9872 98.72%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5801 58.01%
Eye corrosion - 0.9844 98.44%
Eye irritation - 0.7011 70.11%
Skin irritation + 0.5238 52.38%
Skin corrosion - 0.8567 85.67%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8847 88.47%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.5207 52.07%
skin sensitisation - 0.9010 90.10%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6916 69.16%
Acute Oral Toxicity (c) III 0.5087 50.87%
Estrogen receptor binding - 0.5136 51.36%
Androgen receptor binding - 0.6903 69.03%
Thyroid receptor binding - 0.6374 63.74%
Glucocorticoid receptor binding + 0.6348 63.48%
Aromatase binding - 0.7593 75.93%
PPAR gamma - 0.5659 56.59%
Honey bee toxicity - 0.9176 91.76%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.8306 83.06%

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 97.30% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.10% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.40% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.23% 96.61%
CHEMBL221 P23219 Cyclooxygenase-1 86.16% 90.17%
CHEMBL2581 P07339 Cathepsin D 84.38% 98.95%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.76% 95.50%
CHEMBL340 P08684 Cytochrome P450 3A4 80.75% 91.19%

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 71524174
LOTUS LTS0067582
wikiData Q77385042