Furanomycin

Details

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Internal ID a5c846b2-67d8-4ef7-b5d8-73555886d637
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-amino-2-(5-methyl-2,5-dihydrofuran-2-yl)acetic acid
SMILES (Canonical) CC1C=CC(O1)C(C(=O)O)N
SMILES (Isomeric) CC1C=CC(O1)C(C(=O)O)N
InChI InChI=1S/C7H11NO3/c1-4-2-3-5(11-4)6(8)7(9)10/h2-6H,8H2,1H3,(H,9,10)
InChI Key PNOKUGWGMLEAPE-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C7H11NO3
Molecular Weight 157.17 g/mol
Exact Mass 157.07389321 g/mol
Topological Polar Surface Area (TPSA) 72.60 Ų
XlogP -2.80
Atomic LogP (AlogP) -0.26
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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Threomycin
NSC116328
NSC 116328
12794-09-1
NSC-116328
2-Amino-3,6-anhydro-2,4,5,7-tetradeoxyhept-4-enonic acid
SCHEMBL526258
CHEMBL1971558
DTXSID20926031
PNOKUGWGMLEAPE-UHFFFAOYSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Furanomycin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 - 0.8720 87.20%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.3694 36.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.9621 96.21%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9627 96.27%
P-glycoprotein inhibitior - 0.9764 97.64%
P-glycoprotein substrate - 0.9710 97.10%
CYP3A4 substrate - 0.6835 68.35%
CYP2C9 substrate + 0.5898 58.98%
CYP2D6 substrate - 0.8301 83.01%
CYP3A4 inhibition - 0.9426 94.26%
CYP2C9 inhibition - 0.9119 91.19%
CYP2C19 inhibition - 0.8832 88.32%
CYP2D6 inhibition - 0.9555 95.55%
CYP1A2 inhibition - 0.8722 87.22%
CYP2C8 inhibition - 0.9690 96.90%
CYP inhibitory promiscuity - 0.9320 93.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.5555 55.55%
Eye corrosion - 0.9573 95.73%
Eye irritation - 0.6050 60.50%
Skin irritation - 0.6843 68.43%
Skin corrosion - 0.7937 79.37%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8920 89.20%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.7659 76.59%
skin sensitisation - 0.9132 91.32%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.8218 82.18%
Acute Oral Toxicity (c) III 0.5755 57.55%
Estrogen receptor binding - 0.9177 91.77%
Androgen receptor binding - 0.8815 88.15%
Thyroid receptor binding - 0.8415 84.15%
Glucocorticoid receptor binding - 0.8450 84.50%
Aromatase binding - 0.8898 88.98%
PPAR gamma - 0.8318 83.18%
Honey bee toxicity - 0.8943 89.43%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.8323 83.23%

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 96.04% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 83.12% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 81.73% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.21% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.77% 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 272104
LOTUS LTS0207005
wikiData Q82900492