12,12-Dideoxydecarbamoylsaxitoxin

Details

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Internal ID ccab2cfb-ddca-499e-9d61-78e019c31a5b
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines
IUPAC Name [(3aS,4R,10aR)-2,6-diamino-1,3a,4,8,9,10-hexahydropyrrolo[1,2-c]purin-4-yl]methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H16N6O/c10-7-13-6-5(4-16)12-8(11)15-3-1-2-9(6,15)14-7/h5-6,16H,1-4H2,(H2,11,12)(H3,10,13,14)/t5-,6-,9+/m0/s1
InChI Key JFYZIJPKLXIKLJ-ATVXKPNKSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16N6O
Molecular Weight 224.26 g/mol
Exact Mass 224.13855916 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP -2.90
Atomic LogP (AlogP) -2.25
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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DTXSID001335569

2D Structure

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2D Structure of 12,12-Dideoxydecarbamoylsaxitoxin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9478 94.78%
Caco-2 - 0.6284 62.84%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.6580 65.80%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9459 94.59%
OATP1B3 inhibitior + 0.9432 94.32%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.8230 82.30%
P-glycoprotein inhibitior - 0.9549 95.49%
P-glycoprotein substrate - 0.5822 58.22%
CYP3A4 substrate - 0.5667 56.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6645 66.45%
CYP3A4 inhibition - 0.9800 98.00%
CYP2C9 inhibition - 0.9238 92.38%
CYP2C19 inhibition - 0.9376 93.76%
CYP2D6 inhibition - 0.8407 84.07%
CYP1A2 inhibition - 0.9012 90.12%
CYP2C8 inhibition - 0.9383 93.83%
CYP inhibitory promiscuity - 0.9934 99.34%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6042 60.42%
Eye corrosion - 0.9704 97.04%
Eye irritation - 0.9755 97.55%
Skin irritation - 0.6921 69.21%
Skin corrosion - 0.8194 81.94%
Ames mutagenesis - 0.5070 50.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4483 44.83%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5147 51.47%
skin sensitisation - 0.8311 83.11%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.6889 68.89%
Acute Oral Toxicity (c) III 0.6286 62.86%
Estrogen receptor binding - 0.5830 58.30%
Androgen receptor binding - 0.5118 51.18%
Thyroid receptor binding - 0.5667 56.67%
Glucocorticoid receptor binding - 0.5522 55.22%
Aromatase binding - 0.6688 66.88%
PPAR gamma + 0.7204 72.04%
Honey bee toxicity - 0.9223 92.23%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.9529 95.29%

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 95.04% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.27% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.97% 94.45%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 89.05% 95.50%
CHEMBL3012 Q13946 Phosphodiesterase 7A 86.77% 99.29%
CHEMBL3310 Q96DB2 Histone deacetylase 11 84.27% 88.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.96% 95.89%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.81% 90.24%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.61% 96.90%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.41% 90.08%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 146684917
LOTUS LTS0099055
wikiData Q104246544