Diiodohydroxypropane

Details

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Internal ID cd069616-73c3-4272-8502-5cd6ce795e61
Taxonomy Organohalogen compounds > Halohydrins > Iodohydrins
IUPAC Name 1,3-diiodopropan-2-ol
SMILES (Canonical) C(C(CI)O)I
SMILES (Isomeric) C(C(CI)O)I
InChI InChI=1S/C3H6I2O/c4-1-3(6)2-5/h3,6H,1-2H2
InChI Key DNKPFCQEGBJJTE-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C3H6I2O
Molecular Weight 311.89 g/mol
Exact Mass 311.85081 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.22
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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534-08-7
Diiodohydroxypropane
Iopropane
1,3-Diiodo-2-propanol
Iothion
Jothion
Agojodo
Dijodan
Iotone
2-Propanol, 1,3-diiodo-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Diiodohydroxypropane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9648 96.48%
Caco-2 + 0.6003 60.03%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6351 63.51%
OATP2B1 inhibitior - 0.8660 86.60%
OATP1B1 inhibitior + 0.9659 96.59%
OATP1B3 inhibitior + 0.9540 95.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9381 93.81%
P-glycoprotein inhibitior - 0.9869 98.69%
P-glycoprotein substrate - 0.9884 98.84%
CYP3A4 substrate - 0.8206 82.06%
CYP2C9 substrate - 0.8108 81.08%
CYP2D6 substrate - 0.7200 72.00%
CYP3A4 inhibition - 0.9413 94.13%
CYP2C9 inhibition - 0.9049 90.49%
CYP2C19 inhibition - 0.7840 78.40%
CYP2D6 inhibition - 0.9374 93.74%
CYP1A2 inhibition - 0.5345 53.45%
CYP2C8 inhibition - 0.9924 99.24%
CYP inhibitory promiscuity - 0.9308 93.08%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.5962 59.62%
Carcinogenicity (trinary) Non-required 0.5202 52.02%
Eye corrosion + 0.9782 97.82%
Eye irritation + 0.9907 99.07%
Skin irritation + 0.8613 86.13%
Skin corrosion + 0.7390 73.90%
Ames mutagenesis + 0.7117 71.17%
Human Ether-a-go-go-Related Gene inhibition - 0.7223 72.23%
Micronuclear - 0.8841 88.41%
Hepatotoxicity + 0.5909 59.09%
skin sensitisation - 0.6634 66.34%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.5772 57.72%
Acute Oral Toxicity (c) II 0.6685 66.85%
Estrogen receptor binding - 0.9404 94.04%
Androgen receptor binding - 0.9393 93.93%
Thyroid receptor binding - 0.8815 88.15%
Glucocorticoid receptor binding - 0.8708 87.08%
Aromatase binding - 0.8753 87.53%
PPAR gamma - 0.9122 91.22%
Honey bee toxicity - 0.8540 85.40%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.9517 95.17%

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 85.38% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.30% 91.11%

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.
Ainsliaea dissecta
Platycarphella carlinoides
Pulicaria dysenterica
Uncaria homomalla

Cross-Links

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PubChem 68295
NPASS NPC182915