Velutinam

Details

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Internal ID d74b6ec5-5bd5-42a7-b515-0066fdc9a2a3
Taxonomy Alkaloids and derivatives > Aristolactams
IUPAC Name 6-hydroxy-14,15-dimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one
SMILES (Canonical) COC1=C(C2=C3C=CC=C(C3=CC4=C2C(=C1)C(=O)N4)O)OC
SMILES (Isomeric) COC1=C(C2=C3C=CC=C(C3=CC4=C2C(=C1)C(=O)N4)O)OC
InChI InChI=1S/C17H13NO4/c1-21-13-7-10-14-11(18-17(10)20)6-9-8(4-3-5-12(9)19)15(14)16(13)22-2/h3-7,19H,1-2H3,(H,18,20)
InChI Key KUZNZVMKXPBYIB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H13NO4
Molecular Weight 295.29 g/mol
Exact Mass 295.08445790 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.28
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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146428-62-8
CHEMBL519045
AKOS040763391

2D Structure

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2D Structure of Velutinam

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.8011 80.11%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.6242 62.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9387 93.87%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6553 65.53%
P-glycoprotein inhibitior - 0.7760 77.60%
P-glycoprotein substrate - 0.7558 75.58%
CYP3A4 substrate + 0.6264 62.64%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.8230 82.30%
CYP3A4 inhibition - 0.5561 55.61%
CYP2C9 inhibition - 0.7615 76.15%
CYP2C19 inhibition - 0.8844 88.44%
CYP2D6 inhibition - 0.8127 81.27%
CYP1A2 inhibition + 0.8938 89.38%
CYP2C8 inhibition + 0.5346 53.46%
CYP inhibitory promiscuity + 0.6085 60.85%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4510 45.10%
Eye corrosion - 0.9939 99.39%
Eye irritation + 0.5401 54.01%
Skin irritation - 0.8234 82.34%
Skin corrosion - 0.9730 97.30%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6223 62.23%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.5553 55.53%
skin sensitisation - 0.9427 94.27%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.7040 70.40%
Acute Oral Toxicity (c) III 0.4534 45.34%
Estrogen receptor binding + 0.8896 88.96%
Androgen receptor binding + 0.6611 66.11%
Thyroid receptor binding + 0.6756 67.56%
Glucocorticoid receptor binding + 0.8987 89.87%
Aromatase binding + 0.7845 78.45%
PPAR gamma + 0.8294 82.94%
Honey bee toxicity - 0.8622 86.22%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5551 55.51%
Fish aquatic toxicity + 0.8196 81.96%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.93% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.27% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 95.72% 94.75%
CHEMBL2535 P11166 Glucose transporter 94.96% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.48% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.58% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.10% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.49% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.18% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.69% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.44% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.19% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.76% 85.14%
CHEMBL1907 P15144 Aminopeptidase N 87.94% 93.31%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.84% 93.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.43% 99.23%
CHEMBL4208 P20618 Proteasome component C5 85.94% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 84.25% 90.20%
CHEMBL4302 P08183 P-glycoprotein 1 83.47% 92.98%
CHEMBL213 P08588 Beta-1 adrenergic receptor 81.39% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 80.97% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.14% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Fissistigma oldhamii
Goniothalamus amuyon
Goniothalamus griffithii
Goniothalamus velutinus
Uvaria littoralis

Cross-Links

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PubChem 9994639
LOTUS LTS0021720
wikiData Q105146421