(1R,4R,5R,6R,8S,19R)-4-ethenyl-19-hydroxy-4,9,9,20,20-pentamethyl-7-oxa-11-azahexacyclo[14.3.1.05,19.06,8.010,18.012,17]icosa-10(18),12,14,16-tetraene-5-carbonitrile

Details

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Internal ID 16ab19f7-8fa3-4d5d-9280-4f15d1454596
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name (1R,4R,5R,6R,8S,19R)-4-ethenyl-19-hydroxy-4,9,9,20,20-pentamethyl-7-oxa-11-azahexacyclo[14.3.1.05,19.06,8.010,18.012,17]icosa-10(18),12,14,16-tetraene-5-carbonitrile
SMILES (Canonical) CC1(C2CCC(C3(C2(C4=C(C(C5C3O5)(C)C)NC6=CC=CC1=C64)O)C#N)(C)C=C)C
SMILES (Isomeric) C[C@@]1(CC[C@H]2[C@@]3([C@@]1([C@@H]4[C@@H](O4)C(C5=C3C6=C(C2(C)C)C=CC=C6N5)(C)C)C#N)O)C=C
InChI InChI=1S/C26H30N2O2/c1-7-24(6)12-11-16-22(2,3)14-9-8-10-15-17(14)18-19(28-15)23(4,5)20-21(30-20)25(24,13-27)26(16,18)29/h7-10,16,20-21,28-29H,1,11-12H2,2-6H3/t16-,20-,21+,24+,25-,26-/m1/s1
InChI Key AIZZJVVOSLWDHD-ZWCWJZTQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H30N2O2
Molecular Weight 402.50 g/mol
Exact Mass 402.230728204 g/mol
Topological Polar Surface Area (TPSA) 72.30 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.82
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4R,5R,6R,8S,19R)-4-ethenyl-19-hydroxy-4,9,9,20,20-pentamethyl-7-oxa-11-azahexacyclo[14.3.1.05,19.06,8.010,18.012,17]icosa-10(18),12,14,16-tetraene-5-carbonitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9828 98.28%
Caco-2 - 0.5979 59.79%
Blood Brain Barrier + 0.6379 63.79%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.3765 37.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8869 88.69%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8336 83.36%
P-glycoprotein inhibitior - 0.5581 55.81%
P-glycoprotein substrate - 0.6430 64.30%
CYP3A4 substrate + 0.6761 67.61%
CYP2C9 substrate - 0.5894 58.94%
CYP2D6 substrate - 0.7566 75.66%
CYP3A4 inhibition - 0.5370 53.70%
CYP2C9 inhibition - 0.5562 55.62%
CYP2C19 inhibition + 0.5803 58.03%
CYP2D6 inhibition - 0.8018 80.18%
CYP1A2 inhibition + 0.6146 61.46%
CYP2C8 inhibition + 0.6465 64.65%
CYP inhibitory promiscuity + 0.7815 78.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5196 51.96%
Eye corrosion - 0.9844 98.44%
Eye irritation - 0.9414 94.14%
Skin irritation - 0.7652 76.52%
Skin corrosion - 0.9061 90.61%
Ames mutagenesis + 0.5502 55.02%
Human Ether-a-go-go-Related Gene inhibition + 0.6591 65.91%
Micronuclear + 0.5500 55.00%
Hepatotoxicity - 0.5216 52.16%
skin sensitisation - 0.7799 77.99%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.5071 50.71%
Acute Oral Toxicity (c) III 0.5280 52.80%
Estrogen receptor binding + 0.8330 83.30%
Androgen receptor binding + 0.7111 71.11%
Thyroid receptor binding + 0.7923 79.23%
Glucocorticoid receptor binding + 0.7335 73.35%
Aromatase binding + 0.7785 77.85%
PPAR gamma + 0.6219 62.19%
Honey bee toxicity - 0.8158 81.58%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9690 96.90%

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 98.51% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.82% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.13% 96.09%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.29% 85.30%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.69% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.58% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.07% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.91% 89.00%
CHEMBL3310 Q96DB2 Histone deacetylase 11 88.49% 88.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.84% 94.80%
CHEMBL2581 P07339 Cathepsin D 87.10% 98.95%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 87.01% 96.39%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.81% 95.89%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 85.58% 80.96%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.55% 97.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.76% 94.62%
CHEMBL233 P35372 Mu opioid receptor 81.41% 97.93%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.39% 92.94%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 80.22% 89.32%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 44419569
LOTUS LTS0088278
wikiData Q104913057