Kromycin

Details

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Internal ID c3251281-56fa-454d-b0e1-d3efe30d3a61
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (3R,5Z,7S,9R,11Z,13S,14R)-14-ethyl-13-hydroxy-3,5,7,9,13-pentamethyl-1-oxacyclotetradeca-5,11-diene-2,4,10-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O5/c1-7-17-20(6,24)9-8-16(21)13(3)10-12(2)11-14(4)18(22)15(5)19(23)25-17/h8-9,11-13,15,17,24H,7,10H2,1-6H3/b9-8-,14-11-/t12-,13+,15+,17+,20-/m0/s1
InChI Key IUDAFVFBMHXFER-WXIPDEQFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O5
Molecular Weight 350.40 g/mol
Exact Mass 350.20932405 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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20509-23-3
(3R,5Z,7S,9R,11Z,13S,14R)-14-ethyl-13-hydroxy-3,5,7,9,13-pentamethyl-1-oxacyclotetradeca-5,11-diene-2,4,10-trione
((3R-(3R*,5E,7S*,9R*,11E,13S*,14R*))-14-Ethyl-13-hydroxy-3,5,7,9,13-pentamethyloxacyclotetradeca-5,11-diene-2,4,10-trione)

2D Structure

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2D Structure of Kromycin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9870 98.70%
Caco-2 + 0.5205 52.05%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5832 58.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8643 86.43%
OATP1B3 inhibitior + 0.9323 93.23%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5818 58.18%
P-glycoprotein inhibitior - 0.6454 64.54%
P-glycoprotein substrate - 0.6101 61.01%
CYP3A4 substrate + 0.6027 60.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9057 90.57%
CYP3A4 inhibition - 0.7718 77.18%
CYP2C9 inhibition - 0.8855 88.55%
CYP2C19 inhibition - 0.8071 80.71%
CYP2D6 inhibition - 0.9506 95.06%
CYP1A2 inhibition - 0.8207 82.07%
CYP2C8 inhibition - 0.8056 80.56%
CYP inhibitory promiscuity - 0.9418 94.18%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5418 54.18%
Eye corrosion - 0.9709 97.09%
Eye irritation - 0.9399 93.99%
Skin irritation - 0.5193 51.93%
Skin corrosion - 0.8940 89.40%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6680 66.80%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.7338 73.38%
skin sensitisation - 0.5746 57.46%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6846 68.46%
Acute Oral Toxicity (c) III 0.5337 53.37%
Estrogen receptor binding + 0.7614 76.14%
Androgen receptor binding + 0.6056 60.56%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5867 58.67%
Aromatase binding - 0.7697 76.97%
PPAR gamma + 0.6454 64.54%
Honey bee toxicity - 0.8939 89.39%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9319 93.19%

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 94.05% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.17% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.28% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.17% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.08% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.98% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.51% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.04% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.71% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 80.33% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.19% 94.00%

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 6443728
LOTUS LTS0235976
wikiData Q105120489