Ritterazine Q

Details

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Internal ID 1ac0f2fa-5289-437a-becc-2e65fa6fc92d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C54H78N2O7/c1-27-44-40(60-53(27)17-15-46(3,4)62-53)21-34-31-13-11-29-19-36-38(24-48(29,7)33(31)22-42(57)50(34,44)9)55-37-20-30-12-14-32-35(49(30,8)25-39(37)56-36)23-43(58)52(32)26-41-45(51(52,10)59)28(2)54(61-41)18-16-47(5,6)63-54/h27-35,40-42,44-45,57,59H,11-26H2,1-10H3/t27-,28-,29-,30-,31+,32+,33-,34+,35+,40-,41-,42+,44-,45-,48-,49-,50+,51-,52-,53+,54-/m0/s1
InChI Key RPXMJJDFMQEOKE-YVVIHVANSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C54H78N2O7
Molecular Weight 867.20 g/mol
Exact Mass 866.58090283 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP 8.00
Atomic LogP (AlogP) 8.75
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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CHEMBL267199

2D Structure

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2D Structure of Ritterazine Q

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 - 0.8547 85.47%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5904 59.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8808 88.08%
OATP1B3 inhibitior + 0.9000 90.00%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6571 65.71%
BSEP inhibitior + 0.9489 94.89%
P-glycoprotein inhibitior + 0.7562 75.62%
P-glycoprotein substrate + 0.6450 64.50%
CYP3A4 substrate + 0.7426 74.26%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.8052 80.52%
CYP3A4 inhibition - 0.8894 88.94%
CYP2C9 inhibition - 0.9373 93.73%
CYP2C19 inhibition - 0.9024 90.24%
CYP2D6 inhibition - 0.9130 91.30%
CYP1A2 inhibition - 0.6679 66.79%
CYP2C8 inhibition + 0.5969 59.69%
CYP inhibitory promiscuity - 0.9228 92.28%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6125 61.25%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9045 90.45%
Skin irritation - 0.7188 71.88%
Skin corrosion - 0.9219 92.19%
Ames mutagenesis - 0.7264 72.64%
Human Ether-a-go-go-Related Gene inhibition - 0.3627 36.27%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8368 83.68%
Respiratory toxicity + 0.9111 91.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6187 61.87%
Acute Oral Toxicity (c) III 0.5563 55.63%
Estrogen receptor binding + 0.8121 81.21%
Androgen receptor binding + 0.7734 77.34%
Thyroid receptor binding + 0.5453 54.53%
Glucocorticoid receptor binding + 0.7777 77.77%
Aromatase binding + 0.6788 67.88%
PPAR gamma + 0.8024 80.24%
Honey bee toxicity - 0.6905 69.05%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9142 91.42%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.72% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.45% 96.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 93.23% 96.38%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 92.95% 98.99%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.48% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.76% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.00% 92.94%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 88.88% 98.46%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.32% 94.00%
CHEMBL1871 P10275 Androgen Receptor 87.13% 96.43%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.87% 86.33%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 86.19% 98.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.92% 97.09%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 84.65% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.27% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.08% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.96% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.54% 93.04%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.11% 86.00%
CHEMBL332 P03956 Matrix metalloproteinase-1 80.96% 94.50%

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.
Tovaria pendula

Cross-Links

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PubChem 44448219
LOTUS LTS0062053
wikiData Q104970994