MR304A

Details

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Internal ID 0a968bfc-a131-4102-8635-7ec00645f3d8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 2-(1-hydroxyethyl)-4-isocyanocyclopent-4-ene-1,2,3-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H11NO4/c1-4(10)8(13)6(11)3-5(9-2)7(8)12/h3-4,6-7,10-13H,1H3
InChI Key DIACYUPTLLZTEL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H11NO4
Molecular Weight 185.18 g/mol
Exact Mass 185.06880783 g/mol
Topological Polar Surface Area (TPSA) 85.30 Ų
XlogP -1.90
Atomic LogP (AlogP) -1.36
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of MR304A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4670 46.70%
Caco-2 - 0.7723 77.23%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.4542 45.42%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9360 93.60%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9588 95.88%
BSEP inhibitior - 0.9171 91.71%
P-glycoprotein inhibitior - 0.9705 97.05%
P-glycoprotein substrate - 0.8422 84.22%
CYP3A4 substrate - 0.5834 58.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8361 83.61%
CYP3A4 inhibition - 0.9137 91.37%
CYP2C9 inhibition - 0.7876 78.76%
CYP2C19 inhibition - 0.8066 80.66%
CYP2D6 inhibition - 0.9144 91.44%
CYP1A2 inhibition - 0.6893 68.93%
CYP2C8 inhibition - 0.9545 95.45%
CYP inhibitory promiscuity - 0.8001 80.01%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.8123 81.23%
Carcinogenicity (trinary) Non-required 0.5746 57.46%
Eye corrosion - 0.9749 97.49%
Eye irritation - 0.7897 78.97%
Skin irritation - 0.6960 69.60%
Skin corrosion - 0.8658 86.58%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8539 85.39%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.7514 75.14%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5975 59.75%
Acute Oral Toxicity (c) III 0.5784 57.84%
Estrogen receptor binding - 0.8350 83.50%
Androgen receptor binding - 0.6880 68.80%
Thyroid receptor binding - 0.5541 55.41%
Glucocorticoid receptor binding - 0.8393 83.93%
Aromatase binding - 0.8923 89.23%
PPAR gamma - 0.6016 60.16%
Honey bee toxicity - 0.8900 89.00%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.6400 64.00%

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 92.90% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.42% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.44% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.04% 85.14%
CHEMBL221 P23219 Cyclooxygenase-1 82.68% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.06% 95.56%

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 101412407
LOTUS LTS0140891
wikiData Q75063526