4-Guanidino-1-butanol

Details

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Internal ID e9b51b48-0e0b-427e-9302-1825bbe64dff
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Guanidines
IUPAC Name 2-(4-hydroxybutyl)guanidine
SMILES (Canonical) C(CCO)CN=C(N)N
SMILES (Isomeric) C(CCO)CN=C(N)N
InChI InChI=1S/C5H13N3O/c6-5(7)8-3-1-2-4-9/h9H,1-4H2,(H4,6,7,8)
InChI Key FULLTSYFDLSFSF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H13N3O
Molecular Weight 131.18 g/mol
Exact Mass 131.105862047 g/mol
Topological Polar Surface Area (TPSA) 84.60 Ų
XlogP -1.30
Atomic LogP (AlogP) -0.97
H-Bond Acceptor 2
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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2-(4-hydroxybutyl)guanidine
17581-95-2
SCHEMBL1587580
CHEMBL4794818
CHEBI:80947
DTXSID70415728
AKOS006339193
C17146
Q27154918

2D Structure

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2D Structure of 4-Guanidino-1-butanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9059 90.59%
Caco-2 + 0.5143 51.43%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5553 55.53%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9437 94.37%
OATP1B3 inhibitior + 0.9469 94.69%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9644 96.44%
P-glycoprotein inhibitior - 0.9859 98.59%
P-glycoprotein substrate - 0.9271 92.71%
CYP3A4 substrate - 0.7493 74.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7285 72.85%
CYP3A4 inhibition - 0.9240 92.40%
CYP2C9 inhibition - 0.9063 90.63%
CYP2C19 inhibition - 0.9286 92.86%
CYP2D6 inhibition - 0.9322 93.22%
CYP1A2 inhibition - 0.8487 84.87%
CYP2C8 inhibition - 0.9620 96.20%
CYP inhibitory promiscuity - 0.9783 97.83%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5905 59.05%
Eye corrosion - 0.7781 77.81%
Eye irritation + 0.8627 86.27%
Skin irritation + 0.4898 48.98%
Skin corrosion + 0.6294 62.94%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6430 64.30%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.5176 51.76%
skin sensitisation - 0.8252 82.52%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.8217 82.17%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.6570 65.70%
Acute Oral Toxicity (c) III 0.5097 50.97%
Estrogen receptor binding - 0.8896 88.96%
Androgen receptor binding - 0.8654 86.54%
Thyroid receptor binding - 0.8073 80.73%
Glucocorticoid receptor binding - 0.8170 81.70%
Aromatase binding - 0.8160 81.60%
PPAR gamma - 0.9145 91.45%
Honey bee toxicity - 0.9398 93.98%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.8834 88.34%
Fish aquatic toxicity - 0.9853 98.53%

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 93.13% 96.09%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 90.23% 97.88%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.02% 91.11%
CHEMBL204 P00734 Thrombin 89.91% 96.01%
CHEMBL2885 P07451 Carbonic anhydrase III 89.39% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.62% 97.29%
CHEMBL2185 Q96GD4 Serine/threonine-protein kinase Aurora-B 82.24% 96.80%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.17% 99.17%

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.
Leonurus japonicus
Phellodendron chinense

Cross-Links

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PubChem 5317848
NPASS NPC263098