19(E)-11-methoxy-9,18-didemethoxygardneramine

Details

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Internal ID bfe1e269-27b2-49a3-aa34-2266b13f801f
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name (1R,12S,13S,16E,17R,19S)-16-ethylidene-4,5,6-trimethoxy-10-oxa-8,14-diazahexacyclo[11.6.1.01,9.02,7.012,17.014,19]icosa-2,4,6,8-tetraene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26N2O4/c1-5-11-9-24-15-8-22-14-7-16(25-2)19(26-3)20(27-4)18(14)23-21(22)28-10-13(15)12(11)6-17(22)24/h5,7,12-13,15,17H,6,8-10H2,1-4H3/b11-5-/t12-,13-,15-,17-,22+/m0/s1
InChI Key KQEBWWUZXARNSU-GQGWNBIDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26N2O4
Molecular Weight 382.50 g/mol
Exact Mass 382.18925731 g/mol
Topological Polar Surface Area (TPSA) 52.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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(1R,12S,13S,16E,17R,19S)-16-ethylidene-4,5,6-trimethoxy-10-oxa-8,14-diazahexacyclo(11.6.1.01,9.02,7.012,17.014,19)icosa-2,4,6,8-tetraene
(1R,12S,13S,16E,17R,19S)-16-ethylidene-4,5,6-trimethoxy-10-oxa-8,14-diazahexacyclo[11.6.1.01,9.02,7.012,17.014,19]icosa-2,4,6,8-tetraene
RefChem:79423
CHEMBL1782235
CHEBI:67512
Q27135981

2D Structure

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2D Structure of 19(E)-11-methoxy-9,18-didemethoxygardneramine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9494 94.94%
Caco-2 + 0.6847 68.47%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4549 45.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8941 89.41%
OATP1B3 inhibitior + 0.9369 93.69%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.8840 88.40%
P-glycoprotein inhibitior - 0.5112 51.12%
P-glycoprotein substrate + 0.6083 60.83%
CYP3A4 substrate + 0.6554 65.54%
CYP2C9 substrate - 0.7717 77.17%
CYP2D6 substrate + 0.4783 47.83%
CYP3A4 inhibition + 0.5158 51.58%
CYP2C9 inhibition - 0.7627 76.27%
CYP2C19 inhibition - 0.6995 69.95%
CYP2D6 inhibition - 0.8580 85.80%
CYP1A2 inhibition - 0.6301 63.01%
CYP2C8 inhibition + 0.6913 69.13%
CYP inhibitory promiscuity - 0.5732 57.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6019 60.19%
Eye corrosion - 0.9829 98.29%
Eye irritation - 0.9567 95.67%
Skin irritation - 0.7688 76.88%
Skin corrosion - 0.9281 92.81%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8390 83.90%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.5034 50.34%
skin sensitisation - 0.8277 82.77%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.6233 62.33%
Acute Oral Toxicity (c) III 0.6097 60.97%
Estrogen receptor binding + 0.7232 72.32%
Androgen receptor binding + 0.7228 72.28%
Thyroid receptor binding + 0.7210 72.10%
Glucocorticoid receptor binding + 0.8270 82.70%
Aromatase binding - 0.5312 53.12%
PPAR gamma + 0.6135 61.35%
Honey bee toxicity - 0.6907 69.07%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9563 95.63%

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 98.03% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.30% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.72% 94.45%
CHEMBL261 P00915 Carbonic anhydrase I 93.59% 96.76%
CHEMBL5747 Q92793 CREB-binding protein 92.09% 95.12%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.32% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.49% 93.40%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.20% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.09% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.08% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.59% 97.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.55% 96.00%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 82.92% 92.38%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.38% 91.11%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.34% 89.62%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.96% 100.00%

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.
Gardneria ovata

Cross-Links

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PubChem 54582101
LOTUS LTS0115763
wikiData Q27135981