2-(Hydroxymethyl)-1,3-benzodioxole-5-carboxamide

Details

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Internal ID 08e1609a-ec9e-4799-bdc2-a4636161db38
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 2-(hydroxymethyl)-1,3-benzodioxole-5-carboxamide
SMILES (Canonical) C1=CC2=C(C=C1C(=O)N)OC(O2)CO
SMILES (Isomeric) C1=CC2=C(C=C1C(=O)N)OC(O2)CO
InChI InChI=1S/C9H9NO4/c10-9(12)5-1-2-6-7(3-5)14-8(4-11)13-6/h1-3,8,11H,4H2,(H2,10,12)
InChI Key PADJFSLYYLBUOY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H9NO4
Molecular Weight 195.17 g/mol
Exact Mass 195.05315777 g/mol
Topological Polar Surface Area (TPSA) 81.80 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.12
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 2-(Hydroxymethyl)-1,3-benzodioxole-5-carboxamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9817 98.17%
Caco-2 + 0.5837 58.37%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5981 59.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9591 95.91%
OATP1B3 inhibitior + 0.9312 93.12%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9419 94.19%
P-glycoprotein inhibitior - 0.9664 96.64%
P-glycoprotein substrate - 0.9477 94.77%
CYP3A4 substrate - 0.7254 72.54%
CYP2C9 substrate - 0.8083 80.83%
CYP2D6 substrate - 0.8480 84.80%
CYP3A4 inhibition - 0.9534 95.34%
CYP2C9 inhibition - 0.9106 91.06%
CYP2C19 inhibition - 0.8582 85.82%
CYP2D6 inhibition - 0.9128 91.28%
CYP1A2 inhibition - 0.6663 66.63%
CYP2C8 inhibition - 0.8972 89.72%
CYP inhibitory promiscuity - 0.8665 86.65%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5616 56.16%
Eye corrosion - 0.9877 98.77%
Eye irritation + 0.9585 95.85%
Skin irritation - 0.7132 71.32%
Skin corrosion - 0.9345 93.45%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7750 77.50%
Micronuclear + 0.6381 63.81%
Hepatotoxicity - 0.5944 59.44%
skin sensitisation - 0.7976 79.76%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6260 62.60%
Acute Oral Toxicity (c) III 0.6448 64.48%
Estrogen receptor binding - 0.7096 70.96%
Androgen receptor binding - 0.5611 56.11%
Thyroid receptor binding - 0.6460 64.60%
Glucocorticoid receptor binding - 0.8587 85.87%
Aromatase binding - 0.6902 69.02%
PPAR gamma + 0.5804 58.04%
Honey bee toxicity - 0.9720 97.20%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.8238 82.38%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.36% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.03% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.69% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.99% 96.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.25% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.27% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.87% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 80.82% 94.73%

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 101413696
LOTUS LTS0010697
wikiData Q104194138