(1R,13S,16R)-16-hydroxy-5,14-diazapentacyclo[12.3.3.01,13.04,12.06,11]icosa-4(12),6,8,10-tetraen-15-one

Details

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Internal ID 185abb71-423f-4e47-b080-fa7cb579c867
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name (1R,13S,16R)-16-hydroxy-5,14-diazapentacyclo[12.3.3.01,13.04,12.06,11]icosa-4(12),6,8,10-tetraen-15-one
SMILES (Canonical) C1CC23CCC4=C(C2N(C1)C(=O)C(C3)O)C5=CC=CC=C5N4
SMILES (Isomeric) C1C[C@]23CCC4=C([C@H]2N(C1)C(=O)[C@@H](C3)O)C5=CC=CC=C5N4
InChI InChI=1S/C18H20N2O2/c21-14-10-18-7-3-9-20(17(14)22)16(18)15-11-4-1-2-5-12(11)19-13(15)6-8-18/h1-2,4-5,14,16,19,21H,3,6-10H2/t14-,16-,18-/m1/s1
InChI Key KLYJAYKJNHMFJX-QGPMSJSTSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H20N2O2
Molecular Weight 296.40 g/mol
Exact Mass 296.152477885 g/mol
Topological Polar Surface Area (TPSA) 56.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,13S,16R)-16-hydroxy-5,14-diazapentacyclo[12.3.3.01,13.04,12.06,11]icosa-4(12),6,8,10-tetraen-15-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9782 97.82%
Caco-2 + 0.6026 60.26%
Blood Brain Barrier + 0.7007 70.07%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8479 84.79%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9178 91.78%
OATP1B3 inhibitior + 0.9456 94.56%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5564 55.64%
BSEP inhibitior + 0.5629 56.29%
P-glycoprotein inhibitior - 0.9317 93.17%
P-glycoprotein substrate - 0.7358 73.58%
CYP3A4 substrate + 0.6291 62.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7529 75.29%
CYP3A4 inhibition - 0.6713 67.13%
CYP2C9 inhibition - 0.7461 74.61%
CYP2C19 inhibition - 0.7914 79.14%
CYP2D6 inhibition - 0.6156 61.56%
CYP1A2 inhibition - 0.6585 65.85%
CYP2C8 inhibition - 0.8808 88.08%
CYP inhibitory promiscuity - 0.5608 56.08%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6285 62.85%
Eye corrosion - 0.9932 99.32%
Eye irritation - 0.9588 95.88%
Skin irritation - 0.7927 79.27%
Skin corrosion - 0.9400 94.00%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4719 47.19%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5677 56.77%
skin sensitisation - 0.8714 87.14%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.9102 91.02%
Acute Oral Toxicity (c) III 0.4440 44.40%
Estrogen receptor binding + 0.7401 74.01%
Androgen receptor binding + 0.7207 72.07%
Thyroid receptor binding - 0.7378 73.78%
Glucocorticoid receptor binding + 0.6781 67.81%
Aromatase binding + 0.6596 65.96%
PPAR gamma + 0.7104 71.04%
Honey bee toxicity - 0.8372 83.72%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity - 0.6803 68.03%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.75% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.56% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.71% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.39% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.63% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.96% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 89.66% 93.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.39% 97.09%
CHEMBL1914 P06276 Butyrylcholinesterase 88.83% 95.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.74% 89.00%
CHEMBL255 P29275 Adenosine A2b receptor 87.88% 98.59%
CHEMBL3310 Q96DB2 Histone deacetylase 11 87.85% 88.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 86.96% 90.08%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 86.92% 94.08%
CHEMBL4302 P08183 P-glycoprotein 1 86.09% 92.98%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.54% 94.62%
CHEMBL1937 Q92769 Histone deacetylase 2 85.28% 94.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.08% 91.71%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.99% 94.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.99% 85.14%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.15% 93.40%
CHEMBL2535 P11166 Glucose transporter 81.47% 98.75%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 80.87% 95.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.54% 93.04%

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.
Kopsia hainanensis

Cross-Links

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PubChem 54590501
LOTUS LTS0036302
wikiData Q105142863