5-Aminohexane-1,2,3,4,6-pentol

Details

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Internal ID e2cdb8ae-e940-4f12-a8a8-25f02f42c268
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name 5-aminohexane-1,2,3,4,6-pentol
SMILES (Canonical) C(C(C(C(C(CO)O)O)O)N)O
SMILES (Isomeric) C(C(C(C(C(CO)O)O)O)N)O
InChI InChI=1S/C6H15NO5/c7-3(1-8)5(11)6(12)4(10)2-9/h3-6,8-12H,1-2,7H2
InChI Key FQORWEQXRQVPBZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H15NO5
Molecular Weight 181.19 g/mol
Exact Mass 181.09502258 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP -3.40
Atomic LogP (AlogP) -3.62
H-Bond Acceptor 6
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

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2351-14-6
SCHEMBL3797037
DTXSID60313360
NSC269409
NSC-269409

2D Structure

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2D Structure of 5-Aminohexane-1,2,3,4,6-pentol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5850 58.50%
Caco-2 - 0.9731 97.31%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.6807 68.07%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9757 97.57%
OATP1B3 inhibitior - 0.2329 23.29%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9759 97.59%
P-glycoprotein inhibitior - 0.9817 98.17%
P-glycoprotein substrate - 0.9631 96.31%
CYP3A4 substrate - 0.7673 76.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3585 35.85%
CYP3A4 inhibition - 0.9356 93.56%
CYP2C9 inhibition - 0.9237 92.37%
CYP2C19 inhibition - 0.9287 92.87%
CYP2D6 inhibition - 0.8918 89.18%
CYP1A2 inhibition - 0.8595 85.95%
CYP2C8 inhibition - 0.9878 98.78%
CYP inhibitory promiscuity - 0.9773 97.73%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.7239 72.39%
Eye corrosion - 0.8776 87.76%
Eye irritation - 0.9879 98.79%
Skin irritation - 0.7791 77.91%
Skin corrosion - 0.9096 90.96%
Ames mutagenesis - 0.8224 82.24%
Human Ether-a-go-go-Related Gene inhibition - 0.6502 65.02%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.9125 91.25%
skin sensitisation - 0.9398 93.98%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6689 66.89%
Acute Oral Toxicity (c) IV 0.5277 52.77%
Estrogen receptor binding - 0.9225 92.25%
Androgen receptor binding - 0.8378 83.78%
Thyroid receptor binding - 0.6902 69.02%
Glucocorticoid receptor binding - 0.5867 58.67%
Aromatase binding - 0.8722 87.22%
PPAR gamma - 0.8534 85.34%
Honey bee toxicity - 0.9553 95.53%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.9956 99.56%

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 97.29% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.40% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.86% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.53% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.60% 91.11%
CHEMBL2885 P07451 Carbonic anhydrase III 80.29% 87.45%

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 320736
LOTUS LTS0109969
wikiData Q82064351