Lysergyl-L-valyl methyl ester

Details

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Internal ID 933e3773-a1c6-434b-9cfb-c4e56ea3b8bf
Taxonomy Organic acids and derivatives > Peptidomimetics > Hybrid peptides
IUPAC Name methyl 2-[[(6aR,9R)-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carbonyl]amino]-3-methylbutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H27N3O3/c1-12(2)20(22(27)28-4)24-21(26)14-8-16-15-6-5-7-17-19(15)13(10-23-17)9-18(16)25(3)11-14/h5-8,10,12,14,18,20,23H,9,11H2,1-4H3,(H,24,26)/t14-,18-,20?/m1/s1
InChI Key PUSHWZUNZAQTHW-GNTSEGDPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H27N3O3
Molecular Weight 381.50 g/mol
Exact Mass 381.20524173 g/mol
Topological Polar Surface Area (TPSA) 74.40 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.35
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lysergyl-L-valyl methyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9767 97.67%
Caco-2 - 0.6217 62.17%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.9143 91.43%
Subcellular localzation Mitochondria 0.7492 74.92%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.9280 92.80%
OATP1B3 inhibitior + 0.9345 93.45%
MATE1 inhibitior + 0.6387 63.87%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9744 97.44%
P-glycoprotein inhibitior - 0.4709 47.09%
P-glycoprotein substrate + 0.7796 77.96%
CYP3A4 substrate + 0.7881 78.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6969 69.69%
CYP3A4 inhibition - 0.6043 60.43%
CYP2C9 inhibition - 0.7198 71.98%
CYP2C19 inhibition - 0.7006 70.06%
CYP2D6 inhibition - 0.7189 71.89%
CYP1A2 inhibition + 0.6087 60.87%
CYP2C8 inhibition - 0.7525 75.25%
CYP inhibitory promiscuity - 0.5427 54.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6485 64.85%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.9966 99.66%
Skin irritation - 0.7838 78.38%
Skin corrosion - 0.9354 93.54%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9042 90.42%
Micronuclear + 0.7600 76.00%
Hepatotoxicity - 0.6949 69.49%
skin sensitisation - 0.8724 87.24%
Respiratory toxicity + 0.9444 94.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.7829 78.29%
Acute Oral Toxicity (c) III 0.5224 52.24%
Estrogen receptor binding + 0.6463 64.63%
Androgen receptor binding + 0.7926 79.26%
Thyroid receptor binding - 0.4942 49.42%
Glucocorticoid receptor binding + 0.6562 65.62%
Aromatase binding - 0.5478 54.78%
PPAR gamma - 0.5525 55.25%
Honey bee toxicity - 0.8247 82.47%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9889 98.89%

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 99.18% 96.09%
CHEMBL2581 P07339 Cathepsin D 99.07% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 95.03% 91.49%
CHEMBL2535 P11166 Glucose transporter 94.72% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.79% 95.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 93.05% 93.03%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.26% 82.69%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.03% 97.25%
CHEMBL2094135 Q96BI3 Gamma-secretase 91.54% 98.05%
CHEMBL4072 P07858 Cathepsin B 89.16% 93.67%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.15% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.09% 94.45%
CHEMBL217 P14416 Dopamine D2 receptor 87.84% 95.62%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 86.70% 95.71%
CHEMBL5028 O14672 ADAM10 86.51% 97.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.83% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.43% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.77% 93.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.62% 89.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.48% 89.00%
CHEMBL4073 P09237 Matrix metalloproteinase 7 83.16% 97.56%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 82.58% 97.50%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.53% 96.47%
CHEMBL3437 Q16853 Amine oxidase, copper containing 80.15% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.03% 99.23%

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 139583461
LOTUS LTS0018734
wikiData Q75062847