Spiramine Q

Details

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Internal ID 64ab8a7b-ba06-49c1-ad0e-a8ada90453f6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Villanovane, atisane, trachylobane or helvifulvane diterpenoids > Atisane diterpenoids
IUPAC Name (1R,2S,3R,4S,5S,7R,8R,12R,13S,21R)-4,12-dimethyl-14,19-dioxa-17-azaheptacyclo[10.7.2.22,5.02,7.08,18.08,21.013,17]tricosane-3,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H33NO4/c1-19-5-3-6-21-13(19)11-15(27-18(21)23-8-9-26-17(19)23)22-7-4-12(10-14(21)22)20(2,25)16(22)24/h12-18,24-25H,3-11H2,1-2H3/t12-,13+,14-,15+,16-,17-,18?,19+,20-,21-,22+/m0/s1
InChI Key KMFLCNFAUMMLNB-PGOGDVOBSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C22H33NO4
Molecular Weight 375.50 g/mol
Exact Mass 375.24095853 g/mol
Topological Polar Surface Area (TPSA) 62.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Spiramine Q

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7671 76.71%
Caco-2 - 0.5253 52.53%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4613 46.13%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.8887 88.87%
OATP1B3 inhibitior + 0.9487 94.87%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7814 78.14%
BSEP inhibitior + 0.6816 68.16%
P-glycoprotein inhibitior - 0.8604 86.04%
P-glycoprotein substrate - 0.6057 60.57%
CYP3A4 substrate + 0.6878 68.78%
CYP2C9 substrate - 0.6079 60.79%
CYP2D6 substrate - 0.7670 76.70%
CYP3A4 inhibition - 0.9702 97.02%
CYP2C9 inhibition - 0.9265 92.65%
CYP2C19 inhibition - 0.8781 87.81%
CYP2D6 inhibition - 0.9164 91.64%
CYP1A2 inhibition - 0.9436 94.36%
CYP2C8 inhibition - 0.5795 57.95%
CYP inhibitory promiscuity - 0.9559 95.59%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5636 56.36%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9312 93.12%
Skin irritation - 0.7828 78.28%
Skin corrosion - 0.9185 91.85%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.5574 55.74%
skin sensitisation - 0.8648 86.48%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6109 61.09%
Estrogen receptor binding + 0.7665 76.65%
Androgen receptor binding + 0.6563 65.63%
Thyroid receptor binding + 0.6757 67.57%
Glucocorticoid receptor binding + 0.7370 73.70%
Aromatase binding + 0.6677 66.77%
PPAR gamma + 0.5829 58.29%
Honey bee toxicity - 0.7612 76.12%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity - 0.5454 54.54%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.55% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.66% 96.09%
CHEMBL204 P00734 Thrombin 91.42% 96.01%
CHEMBL238 Q01959 Dopamine transporter 90.68% 95.88%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.26% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.86% 82.69%
CHEMBL226 P30542 Adenosine A1 receptor 88.77% 95.93%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 88.76% 100.00%
CHEMBL284 P27487 Dipeptidyl peptidase IV 88.49% 95.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.39% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.30% 92.94%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 88.27% 98.46%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.87% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.57% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 86.23% 95.50%
CHEMBL3012 Q13946 Phosphodiesterase 7A 86.06% 99.29%
CHEMBL237 P41145 Kappa opioid receptor 85.58% 98.10%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 85.42% 90.24%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.32% 93.04%
CHEMBL4073 P09237 Matrix metalloproteinase 7 83.90% 97.56%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 83.49% 98.99%
CHEMBL5028 O14672 ADAM10 82.72% 97.50%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 82.60% 97.50%
CHEMBL2581 P07339 Cathepsin D 82.54% 98.95%
CHEMBL259 P32245 Melanocortin receptor 4 82.30% 95.38%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.25% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.19% 97.14%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.10% 95.17%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.69% 91.03%
CHEMBL3474 P14555 Phospholipase A2 group IIA 81.55% 94.05%

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.
Spiraea japonica

Cross-Links

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PubChem 101915842
LOTUS LTS0037315
wikiData Q105142957