22-Hydroxyacuminatine

Details

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Internal ID badbe538-77e1-4d6e-877a-f3fecacb8171
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Isoquinolones and derivatives
IUPAC Name 19-(hydroxymethyl)-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,10,15,17,19-nonaen-14-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H14N2O2/c23-11-13-5-3-6-15-16(13)9-18-19-14(10-22(18)20(15)24)8-12-4-1-2-7-17(12)21-19/h1-9,23H,10-11H2
InChI Key FIAAPZRVXZOWNP-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C20H14N2O2
Molecular Weight 314.30 g/mol
Exact Mass 314.105527694 g/mol
Topological Polar Surface Area (TPSA) 53.40 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.07
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL205175
19-(hydroxymethyl)-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,10,15,17,19-nonaen-14-one

2D Structure

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2D Structure of 22-Hydroxyacuminatine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.5626 56.26%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7597 75.97%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9384 93.84%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7564 75.64%
BSEP inhibitior + 0.9438 94.38%
P-glycoprotein inhibitior - 0.7301 73.01%
P-glycoprotein substrate - 0.9001 90.01%
CYP3A4 substrate + 0.5866 58.66%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.5513 55.13%
CYP2C9 inhibition - 0.5662 56.62%
CYP2C19 inhibition - 0.8442 84.42%
CYP2D6 inhibition - 0.8769 87.69%
CYP1A2 inhibition + 0.8161 81.61%
CYP2C8 inhibition - 0.6086 60.86%
CYP inhibitory promiscuity + 0.6449 64.49%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6317 63.17%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.8044 80.44%
Skin irritation - 0.7939 79.39%
Skin corrosion - 0.9551 95.51%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7444 74.44%
Micronuclear + 0.8000 80.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8823 88.23%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5562 55.62%
Acute Oral Toxicity (c) III 0.6301 63.01%
Estrogen receptor binding + 0.9449 94.49%
Androgen receptor binding + 0.5893 58.93%
Thyroid receptor binding + 0.6591 65.91%
Glucocorticoid receptor binding + 0.8463 84.63%
Aromatase binding + 0.8672 86.72%
PPAR gamma + 0.9096 90.96%
Honey bee toxicity - 0.9204 92.04%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.7274 72.74%

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
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.73% 93.99%
CHEMBL2581 P07339 Cathepsin D 95.71% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.62% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.34% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.99% 95.56%
CHEMBL1781 P11387 DNA topoisomerase I 91.09% 97.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.92% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.88% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.81% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.32% 96.09%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 87.57% 96.67%
CHEMBL5805 Q9NR97 Toll-like receptor 8 87.09% 96.25%
CHEMBL2535 P11166 Glucose transporter 86.29% 98.75%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 86.09% 95.83%
CHEMBL3401 O75469 Pregnane X receptor 84.94% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.63% 92.62%
CHEMBL220 P22303 Acetylcholinesterase 84.54% 94.45%
CHEMBL1741221 Q9Y4P1 Cysteine protease ATG4B 82.94% 87.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.33% 89.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.76% 93.10%

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.
Camptotheca acuminata

Cross-Links

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PubChem 9883320
LOTUS LTS0205212
wikiData Q104995542