(2S)-2-amino-1-((1,2,3,4,5,6-14C6)cyclohexatrienyl)propan-1-ol

Details

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Internal ID 67b7272d-9166-4f6c-97b4-a862840f0184
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name (2S)-2-amino-1-((1,2,3,4,5,6-14C6)cyclohexatrienyl)propan-1-ol
SMILES (Canonical) CC(C(C1=CC=CC=C1)O)N
SMILES (Isomeric) C[C@@H](C([14C]1=[14CH][14CH]=[14CH][14CH]=[14CH]1)O)N
InChI InChI=1S/C9H13NO/c1-7(10)9(11)8-5-3-2-4-6-8/h2-7,9,11H,10H2,1H3/t7-,9?/m0/s1/i2+2,3+2,4+2,5+2,6+2,8+2
InChI Key DLNKOYKMWOXYQA-DIQCGLEQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H13NO
Molecular Weight 163.16 g/mol
Exact Mass 163.1191660 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2-amino-1-((1,2,3,4,5,6-14C6)cyclohexatrienyl)propan-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.8230 82.30%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.7779 77.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9587 95.87%
OATP1B3 inhibitior + 0.9672 96.72%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9277 92.77%
P-glycoprotein inhibitior - 0.9898 98.98%
P-glycoprotein substrate - 0.9371 93.71%
CYP3A4 substrate - 0.7240 72.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5398 53.98%
CYP3A4 inhibition - 0.9261 92.61%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9859 98.59%
CYP inhibitory promiscuity - 0.9096 90.96%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) + 0.5189 51.89%
Carcinogenicity (trinary) Non-required 0.6955 69.55%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9541 95.41%
Skin irritation - 0.5969 59.69%
Skin corrosion + 0.6347 63.47%
Ames mutagenesis - 0.6236 62.36%
Human Ether-a-go-go-Related Gene inhibition - 0.8453 84.53%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.6653 66.53%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.4858 48.58%
Acute Oral Toxicity (c) III 0.8360 83.60%
Estrogen receptor binding - 0.9615 96.15%
Androgen receptor binding - 0.8441 84.41%
Thyroid receptor binding - 0.8574 85.74%
Glucocorticoid receptor binding - 0.8410 84.10%
Aromatase binding - 0.9400 94.00%
PPAR gamma - 0.8746 87.46%
Honey bee toxicity - 0.9340 93.40%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.8504 85.04%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.69% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.42% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.65% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.04% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.88% 95.56%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.35% 94.08%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.06% 90.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.08% 91.11%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.80% 93.81%
CHEMBL4208 P20618 Proteasome component C5 82.54% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.38% 85.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.00% 93.56%

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.
Ephedra distachya
Ephedra equisetina
Ephedra intermedia
Ephedra sinica

Cross-Links

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PubChem 10080695
NPASS NPC199972