(+)-Galwesine

Details

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Internal ID ec5c60ea-2e17-4294-aa8b-828f8daead64
Taxonomy Alkaloids and derivatives > Amaryllidaceae alkaloids > Homolycorine-type amaryllidaceae alkaloids
IUPAC Name (1S,2S,6R,8S,9R,10S)-9,15,16-trimethoxy-3-methyl-7,11-dioxa-3-azapentacyclo[8.8.0.02,6.06,8.013,18]octadeca-13,15,17-trien-12-one
SMILES (Canonical) CN1CCC23C1C4C(C(C2O3)OC)OC(=O)C5=CC(=C(C=C45)OC)OC
SMILES (Isomeric) CN1CC[C@@]23[C@@H]1[C@H]4[C@@H]([C@H]([C@@H]2O3)OC)OC(=O)C5=CC(=C(C=C45)OC)OC
InChI InChI=1S/C19H23NO6/c1-20-6-5-19-16(20)13-9-7-11(22-2)12(23-3)8-10(9)18(21)25-14(13)15(24-4)17(19)26-19/h7-8,13-17H,5-6H2,1-4H3/t13-,14+,15-,16+,17+,19-/m1/s1
InChI Key DEWDTESPUJQKRF-MPTZMVSHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H23NO6
Molecular Weight 361.40 g/mol
Exact Mass 361.15253745 g/mol
Topological Polar Surface Area (TPSA) 69.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-Galwesine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8427 84.27%
Caco-2 + 0.8406 84.06%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.6324 63.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9106 91.06%
OATP1B3 inhibitior + 0.9332 93.32%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.4617 46.17%
P-glycoprotein inhibitior - 0.4500 45.00%
P-glycoprotein substrate + 0.5366 53.66%
CYP3A4 substrate + 0.6756 67.56%
CYP2C9 substrate - 0.7887 78.87%
CYP2D6 substrate + 0.3869 38.69%
CYP3A4 inhibition - 0.6273 62.73%
CYP2C9 inhibition - 0.8018 80.18%
CYP2C19 inhibition - 0.7000 70.00%
CYP2D6 inhibition - 0.7448 74.48%
CYP1A2 inhibition - 0.7742 77.42%
CYP2C8 inhibition - 0.8603 86.03%
CYP inhibitory promiscuity - 0.8859 88.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5409 54.09%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9589 95.89%
Skin irritation - 0.8009 80.09%
Skin corrosion - 0.9346 93.46%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3972 39.72%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.8449 84.49%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.6068 60.68%
Acute Oral Toxicity (c) III 0.5601 56.01%
Estrogen receptor binding + 0.7701 77.01%
Androgen receptor binding + 0.6460 64.60%
Thyroid receptor binding + 0.6593 65.93%
Glucocorticoid receptor binding + 0.8113 81.13%
Aromatase binding + 0.6085 60.85%
PPAR gamma + 0.6484 64.84%
Honey bee toxicity - 0.7134 71.34%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.6482 64.82%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.75% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.54% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.72% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.90% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 93.20% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.64% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.63% 97.14%
CHEMBL2581 P07339 Cathepsin D 90.07% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.71% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.28% 91.07%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.53% 94.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 86.89% 90.24%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.66% 96.77%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.08% 93.04%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.95% 91.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.55% 94.42%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.29% 89.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.74% 82.38%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.43% 89.50%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 81.65% 98.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.41% 93.03%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.17% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.82% 92.62%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 80.69% 96.86%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.62% 94.78%

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.
Aralia elata var. elata
Galanthus elwesii
Pittosporum eugenioides
Pteroxygonum giraldii

Cross-Links

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PubChem 101927638
NPASS NPC171936
LOTUS LTS0203194
wikiData Q104977569