Caboxamycin

Details

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Internal ID 8f72f3ac-55eb-427c-98c2-e59aec7a3b8e
Taxonomy Organoheterocyclic compounds > Azoles > Oxazoles > Phenyl-1,3-oxazoles
IUPAC Name 2-(2-hydroxyphenyl)-1,3-benzoxazole-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H9NO4/c16-10-6-2-1-4-8(10)13-15-12-9(14(17)18)5-3-7-11(12)19-13/h1-7,16H,(H,17,18)
InChI Key CRLJZJZGYIYVSO-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C14H9NO4
Molecular Weight 255.22 g/mol
Exact Mass 255.05315777 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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4-BENZOXAZOLECARBOXYLIC ACID, 2-(2-HYDROXYPHENYL)-
2-(2-hydroxyphenyl)-1,3-benzoxazole-4-carboxylic acid
2-(2-Hydroxyphenyl)benzo[d]oxazole-4-carboxylic acid
Caboxamycin
starbld0007806
SCHEMBL2959863
CHEMBL3103512
CRLJZJZGYIYVSO-UHFFFAOYSA-N
NSC789942
NSC-789942
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Caboxamycin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 - 0.8100 81.00%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Plasma membrane 0.4943 49.43%
OATP2B1 inhibitior - 0.7003 70.03%
OATP1B1 inhibitior + 0.9476 94.76%
OATP1B3 inhibitior + 0.9018 90.18%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7186 71.86%
P-glycoprotein inhibitior - 0.8580 85.80%
P-glycoprotein substrate - 0.9277 92.77%
CYP3A4 substrate - 0.6581 65.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9073 90.73%
CYP3A4 inhibition - 0.8591 85.91%
CYP2C9 inhibition - 0.7153 71.53%
CYP2C19 inhibition - 0.7097 70.97%
CYP2D6 inhibition - 0.8709 87.09%
CYP1A2 inhibition + 0.8458 84.58%
CYP2C8 inhibition + 0.5278 52.78%
CYP inhibitory promiscuity - 0.7656 76.56%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6121 61.21%
Eye corrosion - 0.9945 99.45%
Eye irritation + 0.7789 77.89%
Skin irritation - 0.7943 79.43%
Skin corrosion - 0.9766 97.66%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9005 90.05%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.7659 76.59%
skin sensitisation - 0.8356 83.56%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.6484 64.84%
Acute Oral Toxicity (c) III 0.5096 50.96%
Estrogen receptor binding + 0.7686 76.86%
Androgen receptor binding + 0.6833 68.33%
Thyroid receptor binding + 0.6845 68.45%
Glucocorticoid receptor binding + 0.8118 81.18%
Aromatase binding + 0.8182 81.82%
PPAR gamma + 0.9176 91.76%
Honey bee toxicity - 0.9388 93.88%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.8152 81.52%

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
CHEMBL3038477 P67870 Casein kinase II alpha/beta 97.04% 99.23%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 95.30% 95.72%
CHEMBL2581 P07339 Cathepsin D 92.42% 98.95%
CHEMBL1811 P34995 Prostanoid EP1 receptor 92.36% 95.71%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 92.13% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.47% 95.56%
CHEMBL230 P35354 Cyclooxygenase-2 87.02% 89.63%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.62% 99.15%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 85.77% 87.67%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 83.29% 83.00%
CHEMBL3401 O75469 Pregnane X receptor 83.28% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.20% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.02% 95.50%
CHEMBL3891 P07384 Calpain 1 82.29% 93.04%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.78% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.74% 96.67%
CHEMBL2535 P11166 Glucose transporter 80.86% 98.75%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.53% 94.42%

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 135957253
LOTUS LTS0033311
wikiData Q77573537