4,5-Didehydroguadiscine

Details

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Internal ID 0d50ca90-20d8-405a-83cf-05705bbb34de
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 16-methoxy-13,13-dimethyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,9,11,14(19),15,17-octaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H17NO3/c1-20(2)14-9-12(22-3)4-5-13(14)17-16-11(6-7-21-19(16)20)8-15-18(17)24-10-23-15/h4-9H,10H2,1-3H3
InChI Key GLMROMLEFUHTEP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H17NO3
Molecular Weight 319.40 g/mol
Exact Mass 319.12084340 g/mol
Topological Polar Surface Area (TPSA) 40.60 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.28
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,5-Didehydroguadiscine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.7777 77.77%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6910 69.10%
OATP2B1 inhibitior - 0.8626 86.26%
OATP1B1 inhibitior + 0.9041 90.41%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7769 77.69%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.7079 70.79%
CYP3A4 substrate + 0.6040 60.40%
CYP2C9 substrate - 0.8076 80.76%
CYP2D6 substrate - 0.7574 75.74%
CYP3A4 inhibition + 0.8272 82.72%
CYP2C9 inhibition + 0.5199 51.99%
CYP2C19 inhibition + 0.7988 79.88%
CYP2D6 inhibition + 0.6076 60.76%
CYP1A2 inhibition + 0.8758 87.58%
CYP2C8 inhibition + 0.6588 65.88%
CYP inhibitory promiscuity + 0.9109 91.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4528 45.28%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.7674 76.74%
Skin irritation - 0.8112 81.12%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis + 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7578 75.78%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.7838 78.38%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.6255 62.55%
Acute Oral Toxicity (c) III 0.5575 55.75%
Estrogen receptor binding + 0.8649 86.49%
Androgen receptor binding + 0.7821 78.21%
Thyroid receptor binding + 0.8673 86.73%
Glucocorticoid receptor binding + 0.7873 78.73%
Aromatase binding + 0.7870 78.70%
PPAR gamma + 0.8405 84.05%
Honey bee toxicity - 0.8141 81.41%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity - 0.3834 38.34%

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 98.59% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.62% 96.77%
CHEMBL2039 P27338 Monoamine oxidase B 97.24% 92.51%
CHEMBL1951 P21397 Monoamine oxidase A 97.12% 91.49%
CHEMBL2243 O00519 Anandamide amidohydrolase 96.32% 97.53%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.19% 94.00%
CHEMBL240 Q12809 HERG 95.02% 89.76%
CHEMBL4208 P20618 Proteasome component C5 94.75% 90.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 94.74% 85.30%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.51% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.86% 86.33%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 93.17% 93.10%
CHEMBL3492 P49721 Proteasome Macropain subunit 92.77% 90.24%
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 91.22% 95.39%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.81% 99.15%
CHEMBL5747 Q92793 CREB-binding protein 90.00% 95.12%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 89.37% 93.24%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 89.15% 82.67%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 88.67% 96.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.25% 94.80%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 88.23% 80.96%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.20% 92.62%
CHEMBL1907 P15144 Aminopeptidase N 87.77% 93.31%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 87.76% 96.67%
CHEMBL2535 P11166 Glucose transporter 87.55% 98.75%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 87.00% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.82% 94.45%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 86.37% 96.39%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 86.06% 85.49%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 85.35% 94.03%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.72% 95.78%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.37% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.12% 95.89%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 83.24% 81.29%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.88% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.52% 93.99%
CHEMBL1907599 P05556 Integrin alpha-4/beta-1 82.44% 92.86%
CHEMBL3401 O75469 Pregnane X receptor 81.97% 94.73%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.43% 96.21%
CHEMBL3706 P78536 ADAM17 80.46% 90.71%

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.
Hornschuchia obliqua

Cross-Links

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PubChem 102286574
LOTUS LTS0177216
wikiData Q105011084