Fosmidomycin

Details

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Internal ID 320ce332-9ff2-4c82-b8d0-a39b8f798b4b
Taxonomy Organic acids and derivatives > Organic phosphonic acids and derivatives > Organic phosphonic acids
IUPAC Name 3-[formyl(hydroxy)amino]propylphosphonic acid
SMILES (Canonical) C(CN(C=O)O)CP(=O)(O)O
SMILES (Isomeric) C(CN(C=O)O)CP(=O)(O)O
InChI InChI=1S/C4H10NO5P/c6-4-5(7)2-1-3-11(8,9)10/h4,7H,1-3H2,(H2,8,9,10)
InChI Key GJXWDTUCERCKIX-UHFFFAOYSA-N
Popularity 334 references in papers

Physical and Chemical Properties

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Molecular Formula C4H10NO5P
Molecular Weight 183.10 g/mol
Exact Mass 183.02965942 g/mol
Topological Polar Surface Area (TPSA) 98.10 Ų
XlogP -2.20
Atomic LogP (AlogP) -0.60
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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66508-53-0
Fosmidomycina
Fosmidomycine
Fosmidomycinum
3-[FORMYL(HYDROXY)AMINO]PROPYLPHOSPHONIC ACID
Fosmidomicina
{3-[formyl(hydroxy)amino]propyl}phosphonic acid
3-(N-hydroxyformamido)propylphosphonic acid
5829E3D9I9
CHEBI:443725
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Fosmidomycin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9659 96.59%
Caco-2 + 0.5236 52.36%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.7724 77.24%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9360 93.60%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9761 97.61%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9382 93.82%
CYP3A4 substrate - 0.5557 55.57%
CYP2C9 substrate - 0.7874 78.74%
CYP2D6 substrate - 0.8290 82.90%
CYP3A4 inhibition - 0.6376 63.76%
CYP2C9 inhibition - 0.8560 85.60%
CYP2C19 inhibition - 0.8218 82.18%
CYP2D6 inhibition - 0.9187 91.87%
CYP1A2 inhibition - 0.7958 79.58%
CYP2C8 inhibition - 0.9795 97.95%
CYP inhibitory promiscuity - 0.9611 96.11%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5819 58.19%
Carcinogenicity (trinary) Non-required 0.5591 55.91%
Eye corrosion - 0.8290 82.90%
Eye irritation + 0.5744 57.44%
Skin irritation - 0.7040 70.40%
Skin corrosion - 0.8189 81.89%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7089 70.89%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8481 84.81%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.6273 62.73%
Acute Oral Toxicity (c) III 0.6064 60.64%
Estrogen receptor binding - 0.8872 88.72%
Androgen receptor binding - 0.9261 92.61%
Thyroid receptor binding - 0.7183 71.83%
Glucocorticoid receptor binding - 0.6303 63.03%
Aromatase binding - 0.7294 72.94%
PPAR gamma - 0.7754 77.54%
Honey bee toxicity - 0.5676 56.76%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.8786 87.86%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.76% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.14% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.08% 92.86%
CHEMBL3401 O75469 Pregnane X receptor 82.01% 94.73%

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 572
LOTUS LTS0041783
wikiData Q905038