Sch 725674

Details

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Internal ID 1fad5209-a28c-47e2-8e06-34a883637454
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (3E)-5,6,8-trihydroxy-14-pentyl-1-oxacyclotetradec-3-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H32O5/c1-2-3-5-9-15-10-7-4-6-8-14(19)13-17(21)16(20)11-12-18(22)23-15/h11-12,14-17,19-21H,2-10,13H2,1H3/b12-11+
InChI Key LEEBEEPDVOWSDN-VAWYXSNFSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C18H32O5
Molecular Weight 328.40 g/mol
Exact Mass 328.22497412 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.47
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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877061-66-0
Antibiotic Sch 725674
(3E)-5,6,8-trihydroxy-14-pentyl-1-oxacyclotetradec-3-en-2-one

2D Structure

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2D Structure of Sch 725674

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8368 83.68%
Caco-2 - 0.6349 63.49%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5763 57.63%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.8480 84.80%
OATP1B3 inhibitior + 0.9315 93.15%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8673 86.73%
P-glycoprotein inhibitior - 0.8920 89.20%
P-glycoprotein substrate - 0.6240 62.40%
CYP3A4 substrate + 0.5446 54.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8878 88.78%
CYP3A4 inhibition - 0.5401 54.01%
CYP2C9 inhibition - 0.9210 92.10%
CYP2C19 inhibition - 0.6251 62.51%
CYP2D6 inhibition - 0.9315 93.15%
CYP1A2 inhibition - 0.7282 72.82%
CYP2C8 inhibition - 0.7920 79.20%
CYP inhibitory promiscuity - 0.9552 95.52%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7169 71.69%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.9661 96.61%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.8893 88.93%
Ames mutagenesis - 0.7878 78.78%
Human Ether-a-go-go-Related Gene inhibition - 0.6021 60.21%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5878 58.78%
skin sensitisation - 0.7661 76.61%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5590 55.90%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.5789 57.89%
Acute Oral Toxicity (c) III 0.4871 48.71%
Estrogen receptor binding + 0.7106 71.06%
Androgen receptor binding - 0.7306 73.06%
Thyroid receptor binding + 0.6457 64.57%
Glucocorticoid receptor binding + 0.5722 57.22%
Aromatase binding - 0.7861 78.61%
PPAR gamma + 0.5916 59.16%
Honey bee toxicity - 0.9756 97.56%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6812 68.12%
Fish aquatic toxicity + 0.9449 94.49%

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 97.50% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 97.00% 89.63%
CHEMBL2581 P07339 Cathepsin D 96.58% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.61% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.45% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.43% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.21% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.72% 100.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.05% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.28% 95.89%
CHEMBL1968 P07099 Epoxide hydrolase 1 82.10% 98.57%
CHEMBL5255 O00206 Toll-like receptor 4 81.86% 92.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.23% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.94% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.90% 99.23%
CHEMBL1871 P10275 Androgen Receptor 80.78% 96.43%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.09% 90.71%

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 11566107
LOTUS LTS0029920
wikiData Q77421233