(4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,26-trimethoxy-4,17-dimethyl-2H-1,24:12,15-dietheno-6,10-metheno-16H-pyrido(2',3':17,18)(1,10)dioxacycloeicosino(2,3,4-ij)isoquinolin-22-ol

Details

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Internal ID bd80afb5-5dfb-4b4b-9582-dede9db588bc
Taxonomy Lignans, neolignans and related compounds
IUPAC Name (1R,14S)-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H40N2O6/c1-38-14-12-24-19-31(42-4)33-21-27(24)28(38)17-23-8-11-30(41-3)32(18-23)44-26-9-6-22(7-10-26)16-29-35-25(13-15-39(29)2)20-34(43-5)36(40)37(35)45-33/h6-11,18-21,28-29,40H,12-17H2,1-5H3/t28-,29+/m1/s1
InChI Key YJRWQNIRFXVBRB-WDYNHAJCSA-N
Popularity 31 references in papers

Physical and Chemical Properties

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Molecular Formula C37H40N2O6
Molecular Weight 608.70 g/mol
Exact Mass 608.28863700 g/mol
Topological Polar Surface Area (TPSA) 72.90 Ų
XlogP 6.30
Atomic LogP (AlogP) 6.86
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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17132-74-0
DTXSID90169059
(1R,14S)-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol
(1R,14S)-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo(22.6.2.29,12.13,7.114,18.027,31.022,33)hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol
RefChem:1050457
DTXCID6091550
(4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,26-trimethoxy-4,17-dimethyl-2H-1,24:12,15-dietheno-6,10-metheno-16H-pyrido(2',3':17,18)(1,10)dioxacycloeicosino(2,3,4-ij)isoquinolin-22-ol
(+)-Homoaromoline
CHEMBL509855
NSC-251213
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,26-trimethoxy-4,17-dimethyl-2H-1,24:12,15-dietheno-6,10-metheno-16H-pyrido(2',3':17,18)(1,10)dioxacycloeicosino(2,3,4-ij)isoquinolin-22-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8474 84.74%
Caco-2 + 0.6904 69.04%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.4795 47.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9264 92.64%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9959 99.59%
P-glycoprotein inhibitior + 0.9397 93.97%
P-glycoprotein substrate + 0.6478 64.78%
CYP3A4 substrate + 0.6726 67.26%
CYP2C9 substrate + 0.7890 78.90%
CYP2D6 substrate + 0.7253 72.53%
CYP3A4 inhibition - 0.8481 84.81%
CYP2C9 inhibition - 0.9517 95.17%
CYP2C19 inhibition - 0.9248 92.48%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.9157 91.57%
CYP2C8 inhibition + 0.5764 57.64%
CYP inhibitory promiscuity - 0.9706 97.06%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6360 63.60%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9410 94.10%
Skin irritation - 0.7831 78.31%
Skin corrosion - 0.9539 95.39%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9157 91.57%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.9500 95.00%
skin sensitisation - 0.8898 88.98%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8937 89.37%
Acute Oral Toxicity (c) III 0.7616 76.16%
Estrogen receptor binding + 0.7501 75.01%
Androgen receptor binding + 0.7261 72.61%
Thyroid receptor binding + 0.6595 65.95%
Glucocorticoid receptor binding + 0.8705 87.05%
Aromatase binding + 0.6137 61.37%
PPAR gamma + 0.6296 62.96%
Honey bee toxicity - 0.7623 76.23%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.7947 79.47%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.54% 96.09%
CHEMBL2056 P21728 Dopamine D1 receptor 95.15% 91.00%
CHEMBL217 P14416 Dopamine D2 receptor 95.07% 95.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.39% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.96% 93.99%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.21% 89.62%
CHEMBL2581 P07339 Cathepsin D 90.80% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.34% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.30% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.95% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.81% 94.45%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.50% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 86.04% 82.38%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.65% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.19% 93.40%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.06% 90.71%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.94% 95.78%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.44% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.25% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.95% 94.00%
CHEMBL4208 P20618 Proteasome component C5 83.56% 90.00%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 83.38% 90.95%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.31% 100.00%
CHEMBL2535 P11166 Glucose transporter 83.07% 98.75%
CHEMBL2413 P32246 C-C chemokine receptor type 1 82.89% 89.50%

Cross-Links

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PubChem 99620
NPASS NPC271013
ChEMBL CHEMBL509855
LOTUS LTS0169974
wikiData Q76009749