11-Hydroxyfistularin 3

Details

Top
Internal ID 592bb5a0-76d6-4009-be7a-ca12194b9fbe
Taxonomy Benzenoids > Phenol ethers
IUPAC Name (5S,6R)-7,9-dibromo-N-[3-[2,6-dibromo-4-[(1R)-2-[[(5S,6R)-7,9-dibromo-6-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,7,9-triene-3-carbonyl]amino]-1-hydroxyethyl]phenoxy]propyl]-6-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,7,9-triene-3-carboxamide
SMILES (Canonical) COC1=C(C(C2(CC(=NO2)C(=O)NCCCOC3=C(C=C(C=C3Br)C(CNC(=O)C4=NOC5(C4)C=C(C(=C(C5O)Br)OC)Br)O)Br)C=C1Br)O)Br
SMILES (Isomeric) COC1=C([C@@H]([C@]2(CC(=NO2)C(=O)NCCCOC3=C(C=C(C=C3Br)[C@H](CNC(=O)C4=NO[C@@]5(C4)C=C(C(=C([C@@H]5O)Br)OC)Br)O)Br)C=C1Br)O)Br
InChI InChI=1S/C31H30Br6N4O10/c1-47-24-16(34)8-30(26(43)21(24)36)10-18(40-50-30)28(45)38-4-3-5-49-23-14(32)6-13(7-15(23)33)20(42)12-39-29(46)19-11-31(51-41-19)9-17(35)25(48-2)22(37)27(31)44/h6-9,20,26-27,42-44H,3-5,10-12H2,1-2H3,(H,38,45)(H,39,46)/t20-,26-,27-,30+,31+/m0/s1
InChI Key KBSNOPQUQMZRHZ-SHNNIKFMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C31H30Br6N4O10
Molecular Weight 1098.00 g/mol
Exact Mass 1097.70007 g/mol
Topological Polar Surface Area (TPSA) 190.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 5.09
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 12

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 11-Hydroxyfistularin 3

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9752 97.52%
Caco-2 - 0.8501 85.01%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6537 65.37%
OATP2B1 inhibitior - 0.5726 57.26%
OATP1B1 inhibitior + 0.8963 89.63%
OATP1B3 inhibitior + 0.9360 93.60%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8721 87.21%
P-glycoprotein inhibitior + 0.7477 74.77%
P-glycoprotein substrate + 0.7403 74.03%
CYP3A4 substrate + 0.6987 69.87%
CYP2C9 substrate - 0.8069 80.69%
CYP2D6 substrate - 0.7782 77.82%
CYP3A4 inhibition - 0.5381 53.81%
CYP2C9 inhibition - 0.6662 66.62%
CYP2C19 inhibition - 0.5850 58.50%
CYP2D6 inhibition - 0.8460 84.60%
CYP1A2 inhibition - 0.6977 69.77%
CYP2C8 inhibition + 0.6095 60.95%
CYP inhibitory promiscuity - 0.7684 76.84%
UGT catelyzed - 0.6841 68.41%
Carcinogenicity (binary) - 0.6710 67.10%
Carcinogenicity (trinary) Non-required 0.4808 48.08%
Eye corrosion - 0.9801 98.01%
Eye irritation - 0.9075 90.75%
Skin irritation - 0.7593 75.93%
Skin corrosion - 0.9182 91.82%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6623 66.23%
Micronuclear + 0.8300 83.00%
Hepatotoxicity - 0.5977 59.77%
skin sensitisation - 0.8196 81.96%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.8388 83.88%
Acute Oral Toxicity (c) III 0.5875 58.75%
Estrogen receptor binding + 0.7978 79.78%
Androgen receptor binding + 0.7115 71.15%
Thyroid receptor binding + 0.5703 57.03%
Glucocorticoid receptor binding + 0.6420 64.20%
Aromatase binding + 0.6734 67.34%
PPAR gamma + 0.7022 70.22%
Honey bee toxicity - 0.8038 80.38%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8011 80.11%

Targets

Top

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 99.34% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.12% 96.09%
CHEMBL240 Q12809 HERG 98.21% 89.76%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.31% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.79% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 94.75% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.75% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.14% 85.14%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 93.14% 95.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.71% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.20% 94.00%
CHEMBL4208 P20618 Proteasome component C5 90.16% 90.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.74% 95.89%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 89.63% 89.67%
CHEMBL3437 Q16853 Amine oxidase, copper containing 88.56% 94.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.06% 91.07%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.38% 91.24%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.01% 100.00%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 85.61% 95.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.70% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.02% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.42% 95.56%
CHEMBL2535 P11166 Glucose transporter 82.96% 98.75%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 82.94% 96.90%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.44% 96.77%
CHEMBL2885 P07451 Carbonic anhydrase III 80.82% 87.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.50% 93.56%
CHEMBL3891 P07384 Calpain 1 80.27% 93.04%

Plants that contains it

Top
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.
Brassica rapa
Lepidium draba

Cross-Links

Top
PubChem 21601943
NPASS NPC84759
LOTUS LTS0112993
wikiData Q105138509