Blastmycetin C

Details

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Internal ID f3d79821-6603-4b6e-ac89-dd5de38786cc
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acid amides
IUPAC Name (1R,10S,13S)-1-hydroxy-13-(hydroxymethyl)-9-methyl-10-propan-2-yl-3,9,12-triazatricyclo[6.6.1.04,15]pentadeca-4(15),5,7-triene-2,11-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H23N3O4/c1-9(2)14-15(22)18-10(8-21)7-17(24)13-11(19-16(17)23)5-4-6-12(13)20(14)3/h4-6,9-10,14,21,24H,7-8H2,1-3H3,(H,18,22)(H,19,23)/t10-,14-,17+/m0/s1
InChI Key QJKOTTLCVZMZOP-RMLVOYDJSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H23N3O4
Molecular Weight 333.40 g/mol
Exact Mass 333.16885622 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.17
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Blastmycetin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6908 69.08%
Caco-2 - 0.5304 53.04%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5083 50.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9343 93.43%
OATP1B3 inhibitior + 0.9365 93.65%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7401 74.01%
P-glycoprotein inhibitior - 0.9488 94.88%
P-glycoprotein substrate + 0.5409 54.09%
CYP3A4 substrate + 0.5976 59.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7251 72.51%
CYP3A4 inhibition - 0.8426 84.26%
CYP2C9 inhibition - 0.8308 83.08%
CYP2C19 inhibition - 0.8672 86.72%
CYP2D6 inhibition - 0.9300 93.00%
CYP1A2 inhibition - 0.7897 78.97%
CYP2C8 inhibition - 0.8161 81.61%
CYP inhibitory promiscuity - 0.8848 88.48%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6620 66.20%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9949 99.49%
Skin irritation - 0.7884 78.84%
Skin corrosion - 0.9346 93.46%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4784 47.84%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.5677 56.77%
skin sensitisation - 0.8540 85.40%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.7798 77.98%
Acute Oral Toxicity (c) III 0.6304 63.04%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding + 0.5956 59.56%
Thyroid receptor binding - 0.5310 53.10%
Glucocorticoid receptor binding - 0.5523 55.23%
Aromatase binding + 0.5221 52.21%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9179 91.79%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.6982 69.82%

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 98.78% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.80% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.92% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.52% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 94.68% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.74% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.49% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 92.04% 97.79%
CHEMBL3310 Q96DB2 Histone deacetylase 11 91.53% 88.56%
CHEMBL299 P17252 Protein kinase C alpha 91.16% 98.03%
CHEMBL226 P30542 Adenosine A1 receptor 90.03% 95.93%
CHEMBL5103 Q969S8 Histone deacetylase 10 87.79% 90.08%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.76% 95.89%
CHEMBL4208 P20618 Proteasome component C5 86.88% 90.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.79% 93.03%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.30% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.24% 86.33%
CHEMBL2535 P11166 Glucose transporter 84.05% 98.75%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 80.96% 89.67%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.96% 90.24%

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 102093881
LOTUS LTS0273459
wikiData Q77514339