Kumusine

Details

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Internal ID a9068279-194d-4144-9ef2-ce48451891bf
Taxonomy Nucleosides, nucleotides, and analogues > 5-deoxyribonucleosides
IUPAC Name 2-(6-amino-2-chloropurin-9-yl)-3,5-dimethyloxolane-3,4-diol
SMILES (Canonical) CC1C(C(C(O1)N2C=NC3=C(N=C(N=C32)Cl)N)(C)O)O
SMILES (Isomeric) CC1C(C(C(O1)N2C=NC3=C(N=C(N=C32)Cl)N)(C)O)O
InChI InChI=1S/C11H14ClN5O3/c1-4-6(18)11(2,19)9(20-4)17-3-14-5-7(13)15-10(12)16-8(5)17/h3-4,6,9,18-19H,1-2H3,(H2,13,15,16)
InChI Key VGXNTNGMCOCQAZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H14ClN5O3
Molecular Weight 299.71 g/mol
Exact Mass 299.0785170 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.09
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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Trachycladine A
NSC 682347
Kumusine
9H-Purin-6-amine, 2-chloro-9-(5-deoxy-2-C-methylpentofuranosyl)-
NSC682347
Adenosine, 2-chloro-5'-deoxy-2'-C-methyl-
2-chloro-9-(5-deoxy-2-c-methylpentofuranosyl)-9h-purin-6-amine
CHEMBL1973929
DTXSID60936977
2-(6-amino-2-chloropurin-9-yl)-3,5-dimethyloxolane-3,4-diol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Kumusine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9739 97.39%
Caco-2 - 0.8456 84.56%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.5246 52.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9177 91.77%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8928 89.28%
P-glycoprotein inhibitior - 0.9102 91.02%
P-glycoprotein substrate - 0.7070 70.70%
CYP3A4 substrate + 0.5178 51.78%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8854 88.54%
CYP3A4 inhibition - 0.8756 87.56%
CYP2C9 inhibition - 0.8302 83.02%
CYP2C19 inhibition - 0.7635 76.35%
CYP2D6 inhibition - 0.9069 90.69%
CYP1A2 inhibition - 0.7983 79.83%
CYP2C8 inhibition - 0.8134 81.34%
CYP inhibitory promiscuity - 0.9334 93.34%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7857 78.57%
Carcinogenicity (trinary) Non-required 0.5094 50.94%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.9760 97.60%
Skin irritation - 0.7781 77.81%
Skin corrosion - 0.9368 93.68%
Ames mutagenesis - 0.5653 56.53%
Human Ether-a-go-go-Related Gene inhibition - 0.8204 82.04%
Micronuclear + 0.9600 96.00%
Hepatotoxicity + 0.6986 69.86%
skin sensitisation - 0.8694 86.94%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.5301 53.01%
Acute Oral Toxicity (c) III 0.6252 62.52%
Estrogen receptor binding + 0.7940 79.40%
Androgen receptor binding + 0.6493 64.93%
Thyroid receptor binding + 0.7096 70.96%
Glucocorticoid receptor binding + 0.6567 65.67%
Aromatase binding + 0.8356 83.56%
PPAR gamma + 0.7929 79.29%
Honey bee toxicity - 0.9480 94.80%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity - 0.4763 47.63%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.00% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.15% 94.00%
CHEMBL221 P23219 Cyclooxygenase-1 90.07% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.72% 96.09%
CHEMBL301 P24941 Cyclin-dependent kinase 2 89.37% 91.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.85% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 87.47% 94.73%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 87.09% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.31% 94.45%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.10% 90.24%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.95% 94.42%
CHEMBL4208 P20618 Proteasome component C5 81.58% 90.00%
CHEMBL3759 Q9H3N8 Histamine H4 receptor 81.19% 93.81%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 80.91% 80.33%
CHEMBL3137261 O14744 PRMT5/MEP50 complex 80.46% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.39% 95.89%

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.
There are no matching plants.

Cross-Links

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PubChem 387981
LOTUS LTS0012345
wikiData Q82913178