Lamellarin-j

Details

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Internal ID ebbeb488-013c-44d8-9fdb-9671b6cdcff2
Taxonomy Organoheterocyclic compounds > Pyrroles > Substituted pyrroles > Phenylpyrroles
IUPAC Name 12-(3,4-dimethoxyphenyl)-7-hydroxy-8,16,17-trimethoxy-4-oxa-1-azapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-2(11),5,7,9,12,14,16,18-octaen-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H27NO8/c1-34-20-7-6-16(11-23(20)36-3)26-27-18-13-22(35-2)19(32)14-21(18)39-30(33)29(27)31-9-8-15-10-24(37-4)25(38-5)12-17(15)28(26)31/h6-7,10-14,32H,8-9H2,1-5H3
InChI Key YHRLGYIZMSRKSI-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C30H27NO8
Molecular Weight 529.50 g/mol
Exact Mass 529.17366682 g/mol
Topological Polar Surface Area (TPSA) 97.60 Ų
XlogP 4.90
Atomic LogP (AlogP) 5.39
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lamellarin-j

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8800 88.00%
Caco-2 - 0.5734 57.34%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6992 69.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9228 92.28%
OATP1B3 inhibitior + 0.9179 91.79%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.5679 56.79%
BSEP inhibitior + 0.8905 89.05%
P-glycoprotein inhibitior + 0.8917 89.17%
P-glycoprotein substrate + 0.5985 59.85%
CYP3A4 substrate + 0.6485 64.85%
CYP2C9 substrate - 0.5815 58.15%
CYP2D6 substrate - 0.8286 82.86%
CYP3A4 inhibition - 0.6071 60.71%
CYP2C9 inhibition - 0.6376 63.76%
CYP2C19 inhibition - 0.5730 57.30%
CYP2D6 inhibition - 0.8010 80.10%
CYP1A2 inhibition + 0.5415 54.15%
CYP2C8 inhibition + 0.7090 70.90%
CYP inhibitory promiscuity + 0.6206 62.06%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5253 52.53%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9331 93.31%
Skin irritation - 0.8173 81.73%
Skin corrosion - 0.9561 95.61%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5507 55.07%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.8948 89.48%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.9357 93.57%
Acute Oral Toxicity (c) III 0.5751 57.51%
Estrogen receptor binding + 0.8918 89.18%
Androgen receptor binding + 0.7384 73.84%
Thyroid receptor binding + 0.6396 63.96%
Glucocorticoid receptor binding + 0.8630 86.30%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7357 73.57%
Honey bee toxicity - 0.7874 78.74%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5249 52.49%
Fish aquatic toxicity - 0.5099 50.99%

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
CHEMBL2581 P07339 Cathepsin D 98.36% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.50% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.91% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 96.75% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.46% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.26% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.62% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.26% 95.56%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 93.48% 95.53%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.63% 96.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 90.01% 95.78%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.39% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.37% 96.21%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.68% 93.03%
CHEMBL2056 P21728 Dopamine D1 receptor 87.41% 91.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.13% 90.71%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.04% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.54% 99.23%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 86.28% 92.38%
CHEMBL5747 Q92793 CREB-binding protein 85.24% 95.12%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.00% 96.67%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.71% 93.99%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 84.66% 90.95%
CHEMBL217 P14416 Dopamine D2 receptor 82.69% 95.62%
CHEMBL3438 Q05513 Protein kinase C zeta 82.24% 88.48%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.99% 99.15%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.91% 80.78%
CHEMBL5314 Q06418 Tyrosine-protein kinase receptor TYRO3 80.59% 96.00%
CHEMBL4208 P20618 Proteasome component C5 80.24% 90.00%

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.
There are no matching plants.

Cross-Links

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PubChem 11466707
LOTUS LTS0121500
wikiData Q105348570