CID 15646822

Details

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Internal ID f45129f2-c284-4966-b38e-3c73e3b0de5b
Taxonomy Phenylpropanoids and polyketides > Saxitoxins, gonyautoxins, and derivatives
IUPAC Name (2-amino-5,10,10-trihydroxy-6-imino-3a,4,8,9-tetrahydro-1H-pyrrolo[1,2-c]purin-4-yl)methoxycarbonylsulfamic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H17N7O8S/c11-6-13-5-4(3-25-8(18)15-26(22,23)24)17(21)7(12)16-2-1-9(19,20)10(5,16)14-6/h4-5,12,19-21H,1-3H2,(H,15,18)(H3,11,13,14)(H,22,23,24)
InChI Key ALRRPAKWGUBPBK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H17N7O8S
Molecular Weight 395.35 g/mol
Exact Mass 395.08593170 g/mol
Topological Polar Surface Area (TPSA) 243.00 Ų
XlogP -4.80
Atomic LogP (AlogP) -4.11
H-Bond Acceptor 11
H-Bond Donor 8
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 15646822

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5932 59.32%
Caco-2 - 0.8277 82.77%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.3509 35.09%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9278 92.78%
OATP1B3 inhibitior + 0.9371 93.71%
MATE1 inhibitior - 0.5800 58.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9018 90.18%
P-glycoprotein inhibitior - 0.7617 76.17%
P-glycoprotein substrate + 0.6080 60.80%
CYP3A4 substrate + 0.6163 61.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7420 74.20%
CYP3A4 inhibition - 0.9425 94.25%
CYP2C9 inhibition - 0.7501 75.01%
CYP2C19 inhibition - 0.7100 71.00%
CYP2D6 inhibition - 0.8617 86.17%
CYP1A2 inhibition - 0.7142 71.42%
CYP2C8 inhibition - 0.7101 71.01%
CYP inhibitory promiscuity - 0.9777 97.77%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6608 66.08%
Carcinogenicity (trinary) Non-required 0.5472 54.72%
Eye corrosion - 0.9752 97.52%
Eye irritation - 0.9716 97.16%
Skin irritation - 0.7525 75.25%
Skin corrosion - 0.9083 90.83%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6780 67.80%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8172 81.72%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6626 66.26%
Acute Oral Toxicity (c) III 0.5416 54.16%
Estrogen receptor binding + 0.6460 64.60%
Androgen receptor binding + 0.6507 65.07%
Thyroid receptor binding + 0.5584 55.84%
Glucocorticoid receptor binding + 0.5430 54.30%
Aromatase binding + 0.5941 59.41%
PPAR gamma + 0.5372 53.72%
Honey bee toxicity - 0.7563 75.63%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6750 67.50%
Fish aquatic toxicity - 0.5104 51.04%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.90% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.25% 96.09%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 95.75% 96.90%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 95.66% 95.50%
CHEMBL284 P27487 Dipeptidyl peptidase IV 92.13% 95.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.13% 94.45%
CHEMBL220 P22303 Acetylcholinesterase 90.97% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.80% 97.09%
CHEMBL5028 O14672 ADAM10 85.33% 97.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.35% 95.56%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.74% 94.33%
CHEMBL2094135 Q96BI3 Gamma-secretase 83.66% 98.05%
CHEMBL1952 P04818 Thymidylate synthase 83.62% 93.53%
CHEMBL261 P00915 Carbonic anhydrase I 83.51% 96.76%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 83.46% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.88% 95.89%
CHEMBL2072 P35499 Sodium channel protein type IV alpha subunit 82.83% 92.32%
CHEMBL340 P08684 Cytochrome P450 3A4 82.72% 91.19%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.59% 93.03%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.47% 100.00%

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 15646822
LOTUS LTS0118715
wikiData Q104914309