Phenprobamate

Details

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Internal ID 190c32f6-44fc-48d0-8263-40b8fb5b5b8a
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 3-phenylpropyl carbamate
SMILES (Canonical) C1=CC=C(C=C1)CCCOC(=O)N
SMILES (Isomeric) C1=CC=C(C=C1)CCCOC(=O)N
InChI InChI=1S/C10H13NO2/c11-10(12)13-8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2,(H2,11,12)
InChI Key CAMYKONBWHRPDD-UHFFFAOYSA-N
Popularity 70 references in papers

Physical and Chemical Properties

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Molecular Formula C10H13NO2
Molecular Weight 179.22 g/mol
Exact Mass 179.094628657 g/mol
Topological Polar Surface Area (TPSA) 52.30 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.71
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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3-Phenylpropyl carbamate
673-31-4
Spantol
Ansepron
Proformiphen
Actiphan
Actozine
Eirenal
Extacol
Nelaxan
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phenprobamate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.8992 89.92%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7239 72.39%
OATP2B1 inhibitior - 0.8638 86.38%
OATP1B1 inhibitior + 0.9469 94.69%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6967 69.67%
P-glycoprotein inhibitior - 0.9822 98.22%
P-glycoprotein substrate - 0.9259 92.59%
CYP3A4 substrate - 0.6105 61.05%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate + 0.3572 35.72%
CYP3A4 inhibition - 0.9597 95.97%
CYP2C9 inhibition - 0.8258 82.58%
CYP2C19 inhibition - 0.7094 70.94%
CYP2D6 inhibition - 0.8271 82.71%
CYP1A2 inhibition + 0.6357 63.57%
CYP2C8 inhibition - 0.6202 62.02%
CYP inhibitory promiscuity - 0.7173 71.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.4643 46.43%
Eye corrosion - 0.9795 97.95%
Eye irritation + 0.8729 87.29%
Skin irritation - 0.6946 69.46%
Skin corrosion - 0.8912 89.12%
Ames mutagenesis - 0.8870 88.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7097 70.97%
Micronuclear + 0.6385 63.85%
Hepatotoxicity + 0.5931 59.31%
skin sensitisation - 0.9144 91.44%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7521 75.21%
Acute Oral Toxicity (c) III 0.7812 78.12%
Estrogen receptor binding - 0.7355 73.55%
Androgen receptor binding - 0.6278 62.78%
Thyroid receptor binding - 0.8320 83.20%
Glucocorticoid receptor binding - 0.6971 69.71%
Aromatase binding - 0.6450 64.50%
PPAR gamma - 0.8022 80.22%
Honey bee toxicity - 0.9603 96.03%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.4240 42.40%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 79.4 nM
79.4 nM
Potency
Potency
via CMAUP
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.84% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.25% 94.62%
CHEMBL2581 P07339 Cathepsin D 91.55% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.73% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.03% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.25% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.03% 91.11%
CHEMBL3891 P07384 Calpain 1 85.92% 93.04%
CHEMBL221 P23219 Cyclooxygenase-1 82.14% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.34% 96.95%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.53% 93.81%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.45% 95.50%

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.
Vigna radiata

Cross-Links

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PubChem 4770
NPASS NPC309279
ChEMBL CHEMBL1079576