(1R,2R,4R,7S)-7-aminocycloheptane-1,2,4-triol

Details

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Internal ID f0fe9d1a-6849-4c7e-b519-52c71afa04d7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclitols and derivatives
IUPAC Name (1R,2R,4R,7S)-7-aminocycloheptane-1,2,4-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H15NO3/c8-5-2-1-4(9)3-6(10)7(5)11/h4-7,9-11H,1-3,8H2/t4-,5+,6-,7-/m1/s1
InChI Key SKJGTWUZWAKYCQ-XZBKPIIZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H15NO3
Molecular Weight 161.20 g/mol
Exact Mass 161.10519334 g/mol
Topological Polar Surface Area (TPSA) 86.70 Ų
XlogP -1.70
Atomic LogP (AlogP) -1.42
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2R,4R,7S)-7-aminocycloheptane-1,2,4-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7384 73.84%
Caco-2 - 0.9469 94.69%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4044 40.44%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9759 97.59%
OATP1B3 inhibitior + 0.9487 94.87%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9705 97.05%
P-glycoprotein inhibitior - 0.9809 98.09%
P-glycoprotein substrate - 0.9072 90.72%
CYP3A4 substrate - 0.6276 62.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4181 41.81%
CYP3A4 inhibition - 0.9669 96.69%
CYP2C9 inhibition - 0.9303 93.03%
CYP2C19 inhibition - 0.9014 90.14%
CYP2D6 inhibition - 0.9371 93.71%
CYP1A2 inhibition - 0.9065 90.65%
CYP2C8 inhibition - 0.9079 90.79%
CYP inhibitory promiscuity - 0.9775 97.75%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.7032 70.32%
Eye corrosion - 0.7783 77.83%
Eye irritation - 0.8342 83.42%
Skin irritation - 0.6925 69.25%
Skin corrosion - 0.7664 76.64%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6594 65.94%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.6092 60.92%
skin sensitisation - 0.8269 82.69%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6964 69.64%
Acute Oral Toxicity (c) III 0.6031 60.31%
Estrogen receptor binding - 0.7747 77.47%
Androgen receptor binding - 0.8047 80.47%
Thyroid receptor binding - 0.7478 74.78%
Glucocorticoid receptor binding - 0.6992 69.92%
Aromatase binding - 0.8114 81.14%
PPAR gamma - 0.8982 89.82%
Honey bee toxicity - 0.8347 83.47%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.9333 93.33%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 96.61% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 92.95% 95.93%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.39% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.99% 96.09%
CHEMBL5331 Q12866 Proto-oncogene tyrosine-protein kinase MER 80.58% 91.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.10% 91.11%

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.
Physalis lagascae

Cross-Links

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PubChem 131080719
LOTUS LTS0153581
wikiData Q105254862