Cyanide ion

Details

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Internal ID 1ab1bbba-8468-44d6-83a1-82bdf01ef872
Taxonomy Homogeneous non-metal compounds > Other non-metal organides > Other non-metal nitrides
IUPAC Name cyanide
SMILES (Canonical) [C-]#N
SMILES (Isomeric) [C-]#N
InChI InChI=1S/CN/c1-2/q-1
InChI Key XFXPMWWXUTWYJX-UHFFFAOYSA-N
Popularity 12,997 references in papers

Physical and Chemical Properties

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Molecular Formula CN-
Molecular Weight 26.02 g/mol
Exact Mass 26.003074004 g/mol
Topological Polar Surface Area (TPSA) 23.80 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.10
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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CYANIDE ION
Isocyanide
57-12-5
Cyanide anion
Nitrile anion
Cyanide ions
Cyanure [French]
Cyanide(1-) ion
Cyanide(1-)
Carbon nitride ion (CN1-)
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyanide ion

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9475 94.75%
Caco-2 + 0.5747 57.47%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Lysosomes 0.5620 56.20%
OATP2B1 inhibitior - 0.8769 87.69%
OATP1B1 inhibitior + 0.9769 97.69%
OATP1B3 inhibitior + 0.9605 96.05%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9421 94.21%
P-glycoprotein inhibitior - 0.9856 98.56%
P-glycoprotein substrate - 0.9972 99.72%
CYP3A4 substrate - 0.8406 84.06%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.8090 80.90%
CYP3A4 inhibition - 0.9614 96.14%
CYP2C9 inhibition - 0.9039 90.39%
CYP2C19 inhibition - 0.9286 92.86%
CYP2D6 inhibition - 0.9521 95.21%
CYP1A2 inhibition - 0.8295 82.95%
CYP2C8 inhibition - 0.9955 99.55%
CYP inhibitory promiscuity - 0.8728 87.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6836 68.36%
Eye corrosion + 0.9893 98.93%
Eye irritation + 0.9704 97.04%
Skin irritation + 0.8777 87.77%
Skin corrosion + 0.7317 73.17%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7992 79.92%
Micronuclear + 0.6232 62.32%
Hepatotoxicity + 0.9000 90.00%
skin sensitisation + 0.6177 61.77%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.7134 71.34%
Acute Oral Toxicity (c) II 0.5346 53.46%
Estrogen receptor binding - 0.9072 90.72%
Androgen receptor binding - 0.9514 95.14%
Thyroid receptor binding - 0.8570 85.70%
Glucocorticoid receptor binding - 0.8917 89.17%
Aromatase binding - 0.8914 89.14%
PPAR gamma - 0.9010 90.10%
Honey bee toxicity - 0.5530 55.30%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.7678 76.78%

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
No predicted targets yet!

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.
Ginkgo biloba
Hordeum vulgare
Linum usitatissimum
Phytolacca acinosa
Phytolacca americana
Portulaca oleracea
Prunus armeniaca
Prunus davidiana
Prunus mandshurica
Prunus mume
Prunus persica
Prunus sibirica

Cross-Links

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PubChem 5975
NPASS NPC100128