alpha-L-fucose 1-phosphate

Details

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Internal ID f2cb48d7-96ec-448d-bc3c-872334045060
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Monosaccharide phosphates
IUPAC Name [(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl] dihydrogen phosphate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H13O8P/c1-2-3(7)4(8)5(9)6(13-2)14-15(10,11)12/h2-9H,1H3,(H2,10,11,12)/t2-,3+,4+,5-,6-/m0/s1
InChI Key PTVXQARCLQPGIR-KGJVWPDLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C6H13O8P
Molecular Weight 244.14 g/mol
Exact Mass 244.03480437 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP -3.20
Atomic LogP (AlogP) -2.08
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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alpha-L-fucopyranose 1-(dihydrogen phosphate)
6-deoxy-1-O-phosphono-alpha-L-galactopyranose
6-deoxy-alpha-L-galactopyranose 1-(dihydrogen phosphate)
alpha-Fuc-1P
CHEBI:6220
SCHEMBL7529773
alpha-l-(-)-fucose 1-phosphate

2D Structure

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2D Structure of alpha-L-fucose 1-phosphate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9383 93.83%
Caco-2 - 0.9024 90.24%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.7230 72.30%
OATP2B1 inhibitior - 0.8608 86.08%
OATP1B1 inhibitior + 0.9573 95.73%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9783 97.83%
P-glycoprotein inhibitior - 0.9384 93.84%
P-glycoprotein substrate - 0.9729 97.29%
CYP3A4 substrate - 0.5552 55.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8544 85.44%
CYP3A4 inhibition - 0.9360 93.60%
CYP2C9 inhibition - 0.9207 92.07%
CYP2C19 inhibition - 0.8704 87.04%
CYP2D6 inhibition - 0.9286 92.86%
CYP1A2 inhibition - 0.8929 89.29%
CYP2C8 inhibition - 0.9708 97.08%
CYP inhibitory promiscuity - 0.9612 96.12%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6308 63.08%
Eye corrosion - 0.9025 90.25%
Eye irritation - 0.9819 98.19%
Skin irritation - 0.6600 66.00%
Skin corrosion - 0.6790 67.90%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6764 67.64%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.7072 70.72%
skin sensitisation - 0.8519 85.19%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6222 62.22%
Acute Oral Toxicity (c) III 0.6189 61.89%
Estrogen receptor binding - 0.6898 68.98%
Androgen receptor binding - 0.8673 86.73%
Thyroid receptor binding + 0.5645 56.45%
Glucocorticoid receptor binding - 0.6439 64.39%
Aromatase binding - 0.6327 63.27%
PPAR gamma - 0.7516 75.16%
Honey bee toxicity - 0.6592 65.92%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6855 68.55%
Fish aquatic toxicity - 0.5169 51.69%

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 92.25% 96.09%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 89.26% 87.67%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.83% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 85.79% 94.73%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.39% 81.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.94% 89.00%

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 439397
LOTUS LTS0091678
wikiData Q105214922