Hydramycin

Details

Top
Internal ID 3ee37db1-81fb-4246-8734-84fb0a718f54
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 2-[1,2-dihydroxy-1-(oxiran-2-yl)ethyl]-11-hydroxy-5-methylnaphtho[2,3-h]chromene-4,7,12-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H16O8/c1-9-5-11-18(20(27)17-10(19(11)26)3-2-4-12(17)24)21-16(9)13(25)6-14(30-21)22(28,8-23)15-7-29-15/h2-6,15,23-24,28H,7-8H2,1H3
InChI Key WZNWUDKIQDIRSR-UHFFFAOYSA-N
Popularity 11,492 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H16O8
Molecular Weight 408.40 g/mol
Exact Mass 408.08451746 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.16
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
CHEMBL1986714
SCHEMBL13799355
NSC648910
NSC-648910
2-[1,2-dihydroxy-1-(oxiran-2-yl)ethyl]-11-hydroxy-5-methylnaphtho[2,3-h]chromene-4,7,12-trione
NCI60_017037

2D Structure

Top
2D Structure of Hydramycin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8671 86.71%
Caco-2 - 0.8404 84.04%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7239 72.39%
OATP2B1 inhibitior - 0.5680 56.80%
OATP1B1 inhibitior + 0.8898 88.98%
OATP1B3 inhibitior + 0.9619 96.19%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5152 51.52%
P-glycoprotein inhibitior - 0.6695 66.95%
P-glycoprotein substrate + 0.5436 54.36%
CYP3A4 substrate + 0.6476 64.76%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8587 85.87%
CYP3A4 inhibition - 0.8726 87.26%
CYP2C9 inhibition - 0.8827 88.27%
CYP2C19 inhibition - 0.7578 75.78%
CYP2D6 inhibition - 0.9002 90.02%
CYP1A2 inhibition - 0.7856 78.56%
CYP2C8 inhibition + 0.4615 46.15%
CYP inhibitory promiscuity - 0.9742 97.42%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5910 59.10%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.8089 80.89%
Skin irritation - 0.7941 79.41%
Skin corrosion - 0.9484 94.84%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6182 61.82%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.5677 56.77%
skin sensitisation - 0.8138 81.38%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7464 74.64%
Acute Oral Toxicity (c) III 0.4893 48.93%
Estrogen receptor binding + 0.9072 90.72%
Androgen receptor binding + 0.7743 77.43%
Thyroid receptor binding - 0.6284 62.84%
Glucocorticoid receptor binding + 0.8445 84.45%
Aromatase binding + 0.7742 77.42%
PPAR gamma + 0.7922 79.22%
Honey bee toxicity - 0.8846 88.46%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8241 82.41%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 98.87% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.45% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.94% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 96.35% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.46% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 95.06% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.06% 99.23%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 90.33% 96.21%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.56% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.06% 99.15%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.40% 96.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.28% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.85% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.11% 93.99%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 84.04% 96.67%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.74% 100.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.08% 83.57%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.92% 100.00%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.75% 98.75%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

Top
PubChem 373075
LOTUS LTS0053935
wikiData Q105327212