(+)-16-Hydroxygalwesine

Details

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Internal ID 72b1c0e0-3f51-403f-b013-190f4dec34ab
Taxonomy Alkaloids and derivatives > Amaryllidaceae alkaloids > Homolycorine-type amaryllidaceae alkaloids
IUPAC Name (1R,2S,6R,8S,9S,10R)-1-hydroxy-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) CN1CCC23C1C4(C(C(C2O3)OC)OC(=O)C5=CC(=C(C=C54)OC)OC)O
SMILES (Isomeric) CN1CC[C@@]23[C@@H]1[C@]4([C@@H]([C@H]([C@@H]2O3)OC)OC(=O)C5=CC(=C(C=C54)OC)OC)O
InChI InChI=1S/C19H23NO7/c1-20-6-5-18-14(27-18)13(25-4)15-19(22,17(18)20)10-8-12(24-3)11(23-2)7-9(10)16(21)26-15/h7-8,13-15,17,22H,5-6H2,1-4H3/t13-,14-,15+,17+,18-,19-/m0/s1
InChI Key GAIZQRCFAUCISE-GBHAUCNQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H23NO7
Molecular Weight 377.40 g/mol
Exact Mass 377.14745207 g/mol
Topological Polar Surface Area (TPSA) 90.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.30
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-16-Hydroxygalwesine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6335 63.35%
Caco-2 + 0.7373 73.73%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.5733 57.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9203 92.03%
OATP1B3 inhibitior + 0.9257 92.57%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.4859 48.59%
P-glycoprotein inhibitior - 0.5175 51.75%
P-glycoprotein substrate + 0.5302 53.02%
CYP3A4 substrate + 0.6742 67.42%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate + 0.4126 41.26%
CYP3A4 inhibition - 0.7739 77.39%
CYP2C9 inhibition - 0.8209 82.09%
CYP2C19 inhibition - 0.7682 76.82%
CYP2D6 inhibition - 0.7635 76.35%
CYP1A2 inhibition - 0.8169 81.69%
CYP2C8 inhibition - 0.9235 92.35%
CYP inhibitory promiscuity - 0.9208 92.08%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5490 54.90%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9446 94.46%
Skin irritation - 0.7993 79.93%
Skin corrosion - 0.9366 93.66%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4762 47.62%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8524 85.24%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.7275 72.75%
Acute Oral Toxicity (c) III 0.5285 52.85%
Estrogen receptor binding + 0.7763 77.63%
Androgen receptor binding + 0.6203 62.03%
Thyroid receptor binding + 0.6085 60.85%
Glucocorticoid receptor binding + 0.7752 77.52%
Aromatase binding + 0.6832 68.32%
PPAR gamma + 0.6541 65.41%
Honey bee toxicity - 0.7579 75.79%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.3905 39.05%

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 96.42% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.80% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.10% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.38% 96.77%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.81% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.37% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.66% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.11% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.07% 98.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.00% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.82% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.47% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.80% 93.40%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.04% 91.11%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.53% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.39% 92.94%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 84.83% 98.00%
CHEMBL4208 P20618 Proteasome component C5 83.47% 90.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 82.43% 82.38%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.10% 99.23%

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 101927636
NPASS NPC194361
LOTUS LTS0095714
wikiData Q105005435