Hidamicin

Details

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Internal ID 43dafa69-f350-4e90-9127-7b9caee3d937
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name 2-[(2S,3R,4S,5S)-2-hydroxy-6-[(1S)-1-[(2S,4R,5S,6S,7R,9S)-7-hydroxy-2-[[(2S)-2-[(2R,3R,5R)-5-[(2R,3R,5S)-2-hydroxy-5-[(1R)-1-hydroxypropyl]-3,5-dimethyloxolan-2-yl]-3-methyloxolan-2-yl]pentan-2-yl]oxymethyl]-2,4,6-trimethyl-1,10-dioxaspiro[4.5]decan-9-yl]ethyl]-4-methoxy-3,5-dimethyloxan-2-yl]acetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C43H76O13/c1-14-16-39(11,37-23(3)17-33(52-37)42(49)24(4)20-40(12,56-42)32(45)15-2)51-22-38(10)19-25(5)43(55-38)28(8)30(44)18-31(53-43)26(6)35-27(7)36(50-13)29(9)41(48,54-35)21-34(46)47/h23-33,35-37,44-45,48-49H,14-22H2,1-13H3,(H,46,47)/t23-,24-,25-,26+,27-,28+,29-,30-,31+,32-,33-,35?,36+,37-,38+,39+,40+,41+,42-,43+/m1/s1
InChI Key JRTJTPMKHDFWCL-WBGBZJCXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C43H76O13
Molecular Weight 801.10 g/mol
Exact Mass 800.52859247 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.41
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 14

Synonyms

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CP 51532
84331-31-7

2D Structure

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2D Structure of Hidamicin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8695 86.95%
Caco-2 - 0.8737 87.37%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.7587 75.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8139 81.39%
OATP1B3 inhibitior + 0.9131 91.31%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6825 68.25%
P-glycoprotein inhibitior + 0.7824 78.24%
P-glycoprotein substrate + 0.7811 78.11%
CYP3A4 substrate + 0.7194 71.94%
CYP2C9 substrate - 0.5947 59.47%
CYP2D6 substrate - 0.8743 87.43%
CYP3A4 inhibition - 0.8053 80.53%
CYP2C9 inhibition - 0.8543 85.43%
CYP2C19 inhibition - 0.9035 90.35%
CYP2D6 inhibition - 0.9489 94.89%
CYP1A2 inhibition - 0.9432 94.32%
CYP2C8 inhibition + 0.6953 69.53%
CYP inhibitory promiscuity - 0.8840 88.40%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6608 66.08%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9090 90.90%
Skin irritation - 0.6548 65.48%
Skin corrosion - 0.9450 94.50%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7234 72.34%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.6626 66.26%
skin sensitisation - 0.9268 92.68%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.8188 81.88%
Acute Oral Toxicity (c) II 0.4929 49.29%
Estrogen receptor binding + 0.6950 69.50%
Androgen receptor binding + 0.7253 72.53%
Thyroid receptor binding - 0.5706 57.06%
Glucocorticoid receptor binding + 0.8007 80.07%
Aromatase binding + 0.6861 68.61%
PPAR gamma + 0.7621 76.21%
Honey bee toxicity - 0.7301 73.01%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.8894 88.94%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.87% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.62% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.36% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.11% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 96.62% 96.95%
CHEMBL2581 P07339 Cathepsin D 96.25% 98.95%
CHEMBL299 P17252 Protein kinase C alpha 96.17% 98.03%
CHEMBL221 P23219 Cyclooxygenase-1 95.39% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.88% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 94.27% 97.79%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.32% 96.61%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.01% 86.33%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 90.78% 92.29%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.73% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.26% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.25% 94.45%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.73% 97.21%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.30% 97.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.21% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.41% 95.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.33% 93.56%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 82.02% 96.90%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.01% 89.34%
CHEMBL2179 P04062 Beta-glucocerebrosidase 81.22% 85.31%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.20% 96.47%
CHEMBL340 P08684 Cytochrome P450 3A4 80.33% 91.19%

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 129011785
LOTUS LTS0051344
wikiData Q105134094