Ghanamycin B

Details

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Internal ID 135fcd4f-3c90-49cf-8add-02d64a036514
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tetracarboxylic acids and derivatives
IUPAC Name dibutyl 2-[2-hydroxy-2-(3-methoxy-3-oxopropyl)-5-oxooxolan-3-ylidene]propanedioate
SMILES (Canonical) CCCCOC(=O)C(=C1CC(=O)OC1(CCC(=O)OC)O)C(=O)OCCCC
SMILES (Isomeric) CCCCOC(=O)C(=C1CC(=O)OC1(CCC(=O)OC)O)C(=O)OCCCC
InChI InChI=1S/C19H28O9/c1-4-6-10-26-17(22)16(18(23)27-11-7-5-2)13-12-15(21)28-19(13,24)9-8-14(20)25-3/h24H,4-12H2,1-3H3
InChI Key XXTJQQDODGUPIM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H28O9
Molecular Weight 400.40 g/mol
Exact Mass 400.17333247 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ghanamycin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9511 95.11%
Caco-2 + 0.6725 67.25%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7742 77.42%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.8805 88.05%
OATP1B3 inhibitior + 0.9608 96.08%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.5763 57.63%
P-glycoprotein inhibitior - 0.6789 67.89%
P-glycoprotein substrate - 0.6250 62.50%
CYP3A4 substrate + 0.6055 60.55%
CYP2C9 substrate - 0.8109 81.09%
CYP2D6 substrate - 0.8942 89.42%
CYP3A4 inhibition - 0.5984 59.84%
CYP2C9 inhibition - 0.8303 83.03%
CYP2C19 inhibition - 0.7824 78.24%
CYP2D6 inhibition - 0.9330 93.30%
CYP1A2 inhibition - 0.7718 77.18%
CYP2C8 inhibition - 0.7060 70.60%
CYP inhibitory promiscuity - 0.9175 91.75%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6552 65.52%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.6303 63.03%
Skin irritation - 0.5981 59.81%
Skin corrosion - 0.9506 95.06%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5579 55.79%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.9247 92.47%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.7159 71.59%
Acute Oral Toxicity (c) III 0.4169 41.69%
Estrogen receptor binding + 0.5989 59.89%
Androgen receptor binding + 0.5390 53.90%
Thyroid receptor binding - 0.5135 51.35%
Glucocorticoid receptor binding + 0.7314 73.14%
Aromatase binding + 0.5200 52.00%
PPAR gamma + 0.6139 61.39%
Honey bee toxicity - 0.9497 94.97%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9606 96.06%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.75% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.67% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.51% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 92.31% 83.82%
CHEMBL255 P29275 Adenosine A2b receptor 92.24% 98.59%
CHEMBL299 P17252 Protein kinase C alpha 89.74% 98.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.21% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 87.41% 90.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.83% 94.33%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.49% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.14% 99.23%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.09% 94.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.07% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.62% 94.45%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.17% 96.90%

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 132571669
LOTUS LTS0223194
wikiData Q104201438