glycero-galacto-Heptose

Details

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Internal ID 5f042b65-baef-4d15-87a1-537dfe5a02e9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Heptoses
IUPAC Name 2,3,4,5,6,7-hexahydroxyheptanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H14O7/c8-1-3(10)5(12)7(14)6(13)4(11)2-9/h1,3-7,9-14H,2H2
InChI Key YPZMPEPLWKRVLD-UHFFFAOYSA-N
Popularity 864 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14O7
Molecular Weight 210.18 g/mol
Exact Mass 210.07395278 g/mol
Topological Polar Surface Area (TPSA) 138.00 Ų
XlogP -3.60
Atomic LogP (AlogP) -4.02
H-Bond Acceptor 7
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

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5328-64-3
RefChem:143776
d-Glycero-d-galacto-heptose
Heptose
D-Mannoheptose
L-glycero-D-gluco-Heptose
2,3,4,5,6,7-hexahydroxyheptanal
BETA-D-GALACTOHEPTOSE
B-D-GALACTOHEPTOSE
D-Glycero-D-galactoheptose
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of glycero-galacto-Heptose

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4790 47.90%
Caco-2 - 0.9386 93.86%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6838 68.38%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9556 95.56%
OATP1B3 inhibitior + 0.9321 93.21%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9802 98.02%
P-glycoprotein inhibitior - 0.9722 97.22%
P-glycoprotein substrate - 0.9659 96.59%
CYP3A4 substrate - 0.7074 70.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7995 79.95%
CYP3A4 inhibition - 0.9065 90.65%
CYP2C9 inhibition - 0.9411 94.11%
CYP2C19 inhibition - 0.9420 94.20%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition - 0.8505 85.05%
CYP2C8 inhibition - 0.9898 98.98%
CYP inhibitory promiscuity - 0.9652 96.52%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.7860 78.60%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9917 99.17%
Skin irritation - 0.7107 71.07%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6555 65.55%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.8625 86.25%
skin sensitisation - 0.9302 93.02%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.5599 55.99%
Acute Oral Toxicity (c) IV 0.6209 62.09%
Estrogen receptor binding - 0.7620 76.20%
Androgen receptor binding - 0.8264 82.64%
Thyroid receptor binding - 0.6190 61.90%
Glucocorticoid receptor binding - 0.4786 47.86%
Aromatase binding - 0.8331 83.31%
PPAR gamma - 0.8643 86.43%
Honey bee toxicity - 0.9657 96.57%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.9800 98.00%
Fish aquatic toxicity - 0.9544 95.44%

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 85.17% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.85% 96.09%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.49% 98.75%

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 219662
LOTUS LTS0106216
wikiData Q82916929