Maniwamycin F

Details

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Internal ID 21521e76-0043-481a-bdc6-b30447967f8f
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Tertiary amines > Trialkylamines
IUPAC Name [(E)-3-carbamoylhex-1-enyl]-(3-hydroxybutan-2-ylimino)-oxidoazanium
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H21N3O3/c1-4-5-10(11(12)16)6-7-14(17)13-8(2)9(3)15/h6-10,15H,4-5H2,1-3H3,(H2,12,16)/b7-6+,14-13?
InChI Key PMGIXDOHMGRTOF-OSVRVEEHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H21N3O3
Molecular Weight 243.30 g/mol
Exact Mass 243.15829154 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.13
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Maniwamycin F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8593 85.93%
Caco-2 - 0.7319 73.19%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6728 67.28%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8991 89.91%
P-glycoprotein inhibitior - 0.9607 96.07%
P-glycoprotein substrate - 0.7775 77.75%
CYP3A4 substrate - 0.5163 51.63%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8749 87.49%
CYP3A4 inhibition - 0.6173 61.73%
CYP2C9 inhibition - 0.7436 74.36%
CYP2C19 inhibition - 0.7203 72.03%
CYP2D6 inhibition - 0.8856 88.56%
CYP1A2 inhibition - 0.7503 75.03%
CYP2C8 inhibition - 0.9280 92.80%
CYP inhibitory promiscuity - 0.8480 84.80%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.6000 60.00%
Carcinogenicity (trinary) Danger 0.5187 51.87%
Eye corrosion - 0.9690 96.90%
Eye irritation - 0.9965 99.65%
Skin irritation - 0.7455 74.55%
Skin corrosion - 0.9251 92.51%
Ames mutagenesis - 0.5254 52.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7754 77.54%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8197 81.97%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6328 63.28%
Acute Oral Toxicity (c) III 0.5871 58.71%
Estrogen receptor binding - 0.8170 81.70%
Androgen receptor binding - 0.6450 64.50%
Thyroid receptor binding - 0.6409 64.09%
Glucocorticoid receptor binding - 0.6227 62.27%
Aromatase binding - 0.6257 62.57%
PPAR gamma - 0.7487 74.87%
Honey bee toxicity - 0.8985 89.85%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.4793 47.93%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.40% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.56% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.50% 97.25%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.74% 89.34%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.50% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.15% 94.45%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.29% 100.00%
CHEMBL2094135 Q96BI3 Gamma-secretase 87.78% 98.05%
CHEMBL2885 P07451 Carbonic anhydrase III 86.98% 87.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.51% 96.95%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 86.15% 92.29%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.36% 96.61%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.25% 91.81%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.24% 96.47%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.19% 97.29%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 83.93% 97.88%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.85% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.83% 96.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.31% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.04% 90.71%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.49% 92.86%

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 139589374
LOTUS LTS0224620
wikiData Q105211443