Galactitol

Details

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Internal ID 3f60cac1-cde4-4066-9954-3cd285af579e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Sugar alcohols
IUPAC Name (2R,3S,4R,5S)-hexane-1,2,3,4,5,6-hexol
SMILES (Canonical) C(C(C(C(C(CO)O)O)O)O)O
SMILES (Isomeric) C([C@H]([C@@H]([C@@H]([C@H](CO)O)O)O)O)O
InChI InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5+,6-
InChI Key FBPFZTCFMRRESA-GUCUJZIJSA-N
Popularity 3,478 references in papers

Physical and Chemical Properties

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Molecular Formula C6H14O6
Molecular Weight 182.17 g/mol
Exact Mass 182.07903816 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP -3.10
Atomic LogP (AlogP) -3.59
H-Bond Acceptor 6
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

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galactitol
608-66-2
dulcite
Euonymit
D-Galactitol
dulcose
Melampyrin
Melampyrit
D-Dulcitol
(2R,3S,4R,5S)-Hexane-1,2,3,4,5,6-hexaol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Galactitol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6800 68.00%
Caco-2 - 0.9372 93.72%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.5618 56.18%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9744 97.44%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9773 97.73%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.9861 98.61%
CYP3A4 substrate - 0.8126 81.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7541 75.41%
CYP3A4 inhibition - 0.9402 94.02%
CYP2C9 inhibition - 0.9419 94.19%
CYP2C19 inhibition - 0.9232 92.32%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.8240 82.40%
CYP2C8 inhibition - 0.9969 99.69%
CYP inhibitory promiscuity - 0.9580 95.80%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6932 69.32%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9541 95.41%
Skin irritation - 0.7100 71.00%
Skin corrosion - 0.9677 96.77%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5933 59.33%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.9875 98.75%
skin sensitisation - 0.9251 92.51%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.4682 46.82%
Acute Oral Toxicity (c) IV 0.6451 64.51%
Estrogen receptor binding - 0.9264 92.64%
Androgen receptor binding - 0.8313 83.13%
Thyroid receptor binding - 0.7258 72.58%
Glucocorticoid receptor binding - 0.5915 59.15%
Aromatase binding - 0.8514 85.14%
PPAR gamma - 0.8799 87.99%
Honey bee toxicity - 0.9599 95.99%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity - 0.9745 97.45%

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 86.12% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 84.35% 83.82%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.26% 97.29%

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.
Adenopeltis serrata
Aesculus turbinata
Aglaia elaeagnoidea
Alcea rosea
Alisma plantago-aquatica subsp. orientale
Alnus alnobetula
Alpinia roxburghii
Ampelopsis japonica
Argyreia nervosa
Aristolochia littoralis
Artocarpus styracifolius
Astragalus brachycarpus
Astragalus gummifer
Balanops australiana
Bituminaria bituminosa
Buddleja officinalis
Cajanus cajan
Cannabis sativa
Cardiospermum halicacabum
Carum carvi
Cassytha filiformis
Celastrus angulata
Celastrus orbiculatus
Centaurea nigrescens
Centaurea seridis
Chrozophora tinctoria
Cirsium japonicum
Cistanche deserticola
Cistanche phelypaea
Cneorum pulverulentum
Cocos nucifera
Coreopsis fasciculata
Crepis foetida
Crinum viviparum
Cuphea carthagenensis
Dalbergia stipulacea
Davallia perdurans
Delphinium ajacis
Dioscoreophyllum cumminsii
Dorstenia lindeniana
Dorstenia mannii
Elaeagnus commutata
Elaeodendron croceum
Elaeodendron transvaalense
Erigeron canadensis
Eucalyptus flocktoniae
Euonymus tingens
Euphorbia cornigera
Euphorbia segetalis
Flindersia brayleyana
Forsythia giraldiana
Garcinia celebica
Globba racemosa
Gonzalezia decurrens
Heracleum sphondylium
Homalomena occulta
Hylocomium splendens
Jungermannia obovata
Kokoona reflexa
Krameria erecta
Kummerowia striata
Lagotis brevituba
Litchi chinensis
Lophopetalum javanicum
Maesa ramentacea
Mascarenhasia arborescens
Meconopsis napaulensis
Melampyrum chlorostachyum
Melampyrum elatius
Merremia umbellata
Millettia conraui
Millettia laurentii
Monodora tenuifolia
Nectandra amazonum
Ocimum tenuiflorum
Ozoroa insignis
Pachyrhizus erosus
Palafoxia rosea
Parastrephia lepidophylla
Pedicularis condensata
Penstemon secundiflorus
Perityle vaseyi
Phedimus kamtschaticus
Phlogacanthus thyrsiformis
Phoebe formosana
Phytolacca acinosa
Piloselloides hirsuta
Pinus strobus
Pinus sylvestris
Piper arboreum
Plectranthus garckeanus
Plenckia populnea
Pleurostylia opposita
Pluchea odorata
Porella swartziana
Pouzolzia occidentalis
Prunus spinosa
Punica granatum
Quercus mongolica
Rheum webbianum
Ruta microcarpa
Salacia chinensis
Salacia lehmbachii
Salacia reticulata
Salvia coulteri
Salvia yosgadensis
Satureja cuneifolia
Scutellaria przewalskii
Selinum carvifolium
Semialarium mexicanum
Senecio flavus
Sida cordifolia
Sidastrum multiflorum
Sideritis brevibracteata
Sideroxylon cubense
Solanum sisymbriifolium
Swertia diluta
Syncolostemon parviflorus
Tadehagi triquetrum
Thuja plicata
Thymbra spicata
Triglochin maritima
Turraeanthus mannii
Urtica triangularis
Vahlia capensis
Veronica hederifolia
Veronica persica
Zanthoxylum schreberi

Cross-Links

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PubChem 11850
NPASS NPC293908
LOTUS LTS0012947
wikiData Q420367