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Organic compounds
Amidines are organic compounds with the functional group RC(NR)NR2, where the R groups can be the same or different. They are the imine derivatives of
Amidine
Reaction of cyanide and alcohol to give imino ester salt
excess of alcohol to form an orthoester With ammonia or an amine to form an amidine (di-nitriles may form imidines, for instance succinimidine from succinonitrile)
Pinner_reaction
Chemical compound
more commonly DBU, is a chemical compound and belongs to the class of amidine compounds. It is used in organic synthesis as a catalyst, a complexing
1,8-Diazabicyclo(5.4.0)undec-7-ene
1,8-Diazabicyclo(5.4.0)undec-7-ene
Aromatic compound (C4H4N2)
Pinner, who synthesized derivatives by condensing ethyl acetoacetate with amidines. Pinner first proposed the name “pyrimidin” in 1885. The parent compound
Pyrimidine
Chemical compound
N’-tetramethylchloroformamidinium hexafluorophosphate) is an electrophilic amidine reagent used to activate a number of functional groups (such as carboxylic
TCFH
Chemical compound
conjugate addition of the amidine nitrogen to the malononitrile followed by loss of ethoxide (3); addition of the remaining amidine nitrogen to one of the
Amprolium
Chemical compound
compounds. It is the hydrochloride of acetamidine, one of the simplest amidines. Acetamidine hydrochloride is a hygroscopic solid which forms colourless
Acetamidine_hydrochloride
Anti-parasite drug with a di-amidine
certain bacteria including Brucella and Streptococcus. Chemically it is a di-amidine and it is formulated as its aceturate salt, diminazene aceturate. The mechanism
Diminazene
Organic compound
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Urea
Pharmaceutical compound
BB-Cl-Amidine is an experimental drug which acts as a non-subtype selective, irreversible inhibitor of the enzyme peptidylarginine deiminase (PAD). It
BB-Cl-Amidine
Organic compounds of the form >C=O
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Ketone
Chemical compound
0]non-5-ene (DBN) is a chemical compound with the formula C7H12N2. It is an amidine base used in organic synthesis. A related compound with related functions
1,5-Diazabicyclo(4.3.0)non-5-ene
1,5-Diazabicyclo(4.3.0)non-5-ene
Extremely strong base
kcal/mol) than proton sponge. Common superbases of this variety feature amidine, guanidine, and phosphazene functional groups. Strong superbases can be
Superbase
Chemical compound
this group is that of an imine, and the group is related structurally to amidines and ureas. Examples of guanidines are arginine, triazabicyclodecene, saxitoxin
Guanidine
Chemical compound
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Glycidamide
Enzyme
that the rodent proteins are special. Irreversible inhibitors Cl-amidine, BB-Cl-Amidine, YW3-56 Reversible inhibitors GSK484, GSK199 Sams, K.L; Mukai, C;
Protein-arginine_deiminase
Chemical compounds with the structure R–O–O–R'
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Peroxide
Chemical compounds and groups containing nitrogen with a lone pair (:N)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Amine
Any organic compound having a sulfanyl group (–SH)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Thiol
Compound derived from an acid
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Ester
Chemical group (–OC(O)CH3)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Acetoxy_group
Chemical property
R. Caminiti, A. Pieretti, L. Bencivenni, F. Ramondo, N. Sanna (1996). "Amidine N−C(N)−N Skeleton: Its Structure in Isolated and Hydrogen-Bonded Guanidines
Aromaticity
Antiviral medication
liver-targeting than ribavirin. The first property is due to taribavirin's basic amidine group which inhibits drug entry into RBCs, and the second property is probably
Ribavirin
Chemical compound
synthesis (named after Adolf Pinner) the reactants are an alkyl or aryl amidine and phosgene. Insertion of an N-H moiety into a hydrazide by a copper carbenoid
1,3,5-Triazine
Chemical group (–OH)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Hydroxy_group
Organic compound containing C–PO(OR)2 groups
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Phosphonate
Chemical group (>N–C(=O)–O–)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Carbamate
Chemical group (–CH=CH2)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Vinyl_group
Species of flowering plant in the nightshade family
tetrahydroharmine, harmaline, manacin, manacein, and dimethyltryptamine and amidine derivatives such as pyrrole 3-carboxamidine. Cultivated plant, Chicago
Brunfelsia_pauciflora
Chemical compound
2-Iminothiolane reacts with primary amines efficiently at pH 7 to 9, creating amidine compounds with a sulfhydryl group. Thus it allows for crosslinking or labeling
2-Iminothiolane
Group of atoms giving a molecule characteristic properties
carboxamido- or carbamoyl- -amide Acetamide (Ethanamide) Amidine Amidine R4C(NR1)(NR2R3) amidino- -amidine acetamidine (acetimidamide) Guanidine Guanidine RNC(NR2)2)
Functional_group
Chemical group (–CH2–C6H5)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Benzyl_group
Chemical compound
dihydrochloride salt. It binds free amino groups at pH range 7.0-10.0 to form amidine bonds. DMP is used mainly as bifunctional coupling reagent to link proteins
Dimethyl_pimelimidate
Cyclic chemical group (–C6H5)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Phenyl_group
Class of chemical compounds
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Selenol
Organic compound containing the functional group R–CH=O
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Aldehyde
Functional group with the chemical structure R–S–S–R′
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Disulfide
Organic compounds made of alkyl/aryl groups bound to oxygen (R–O–R')
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Ether
Chemical compound
Intermediate aryl amidine (2) is prepared by aluminium trichloride-catalyzed addition of aniline to the nitrile of 4-cyanothiazole (1). The amidine (2) is then
Tiabendazole
Functional group (C=O)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Carbonyl_group
Chemical group (–N=C=O)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Isocyanate
Chemical group derived from alkanes (one hydrogen removed)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Alkyl_group
Benzodiazepine
of bromazepam (1) with methylamine and titanium tetrachloride gives the amidine (2). Treatment with nitrous acid gives the nitrosylation product (3). Further
Pyrazolam
Simplest secondary alcohol
derivatives Ethacridine lactate 9-Aminoacridine Euflavine Biguanides and amidines Dibrompropamidine Chlorhexidine# Propamidine Hexamidine Polihexanide Phenol
Isopropyl_alcohol
Organic compounds of the form RC(=O)NR′R″
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Amide
Organic molecule with two different functional groups
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Bifunctionality
Chemical compound
discovered that sulfur dicyanide reacts with ammonia à la Pinner to give an amidine without displacing the S–C linkage, although dimethylamine induces decomposition
Sulfur_dicyanide
Chemical group (–CH3) derived from methane
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Methyl_group
Chemical compound
derivatives Ethacridine lactate 9-Aminoacridine Euflavine Biguanides and amidines Dibrompropamidine Chlorhexidine# Propamidine Hexamidine Polihexanide Phenol
Sodium_hypochlorite
Urinary antiseptic drug
derivatives Ethacridine lactate 9-Aminoacridine Euflavine Biguanides and amidines Dibrompropamidine Chlorhexidine# Propamidine Hexamidine Polihexanide Phenol
Methenamine
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Reductone
Chemical compound
derivatives Ethacridine lactate 9-Aminoacridine Euflavine Biguanides and amidines Dibrompropamidine Chlorhexidine# Propamidine Hexamidine Polihexanide Phenol
Silver_nitrate
Chemical group, –C(=O)CH3
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Acetyl_group
Surfactant and antiseptic agent
derivatives Ethacridine lactate 9-Aminoacridine Euflavine Biguanides and amidines Dibrompropamidine Chlorhexidine# Propamidine Hexamidine Polihexanide Phenol
Benzalkonium_chloride
Organic compounds of the form >C=N–OH
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Oxime
Organic compounds with a carbon-carbon-oxygen ring
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Epoxide
Organic compound containing a –C(=O)OH group
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Carboxylic_acid
Organic compounds with the structure R–S(=O)2–OH
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Sulfonic_acid
Hydrocarbon compound containing one or more C=C bonds
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Alkene
Drug discovery
selective binding to FXa. Those early developed small molecules yet had amidine-groups or even higher-basic functions, which were thought to be necessary
Discovery and development of direct Xa inhibitors
Discovery_and_development_of_direct_Xa_inhibitors
Chemical compound
derivatives Ethacridine lactate 9-Aminoacridine Euflavine Biguanides and amidines Dibrompropamidine Chlorhexidine# Propamidine Hexamidine Polihexanide Phenol
Hydrogen_peroxide
Chemical group (–CH2–)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Methylene_group
Atypical antipsychotic medication
Olanzapine, sold under the brand name Zyprexa among others, is an atypical antipsychotic primarily used to treat schizophrenia and bipolar disorder. It
Olanzapine
Organic compound with at least one hydroxyl (–OH) group
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Alcohol_(chemistry)
Chemical group (–C3H7) derived from propane
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Propyl_group
Class of organic compounds
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Chlorofluorocarbon
Chemical compound
FGAR + tetrahydrofolate The biosynthesis pathway next converts FGAR to an amidine by the action of phosphoribosylformylglycinamidine synthase (EC 6.3.5.3)
Phosphoribosyl-N-formylglycineamide
Phosphoribosyl-N-formylglycineamide
Chemical group (–CH2–CH=CH2)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Allyl_group
Chemical compound
is likely similar to the Pinner reaction; preceding via an intermediate amidine. Limited research has been done into identifying alternative solvents or
Oxazoline
Hydrocarbon compound (H2C=CH2)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Ethylene
Unstable oxoacid of sulfur
dioxide in an alkaline solution. To do this, thiourea dioxide first forms an amidine-sulfinic acid tautomer, H2NC(=NH)SO2H, which then breaks apart. Sulfoxylate
Sulfoxylic_acid
Medication that reduces stomach acid
Famotidine, sold under the brand name Pepcid among others, is a histamine H2 receptor antagonist medication that decreases stomach acid production. It
Famotidine
Hydrocarbon compound (C6H6)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Benzene
Organic compound (C6H5OH)
derivatives Ethacridine lactate 9-Aminoacridine Euflavine Biguanides and amidines Dibrompropamidine Chlorhexidine# Propamidine Hexamidine Polihexanide Phenol
Phenol
Obsolete sedative–hypnotic drug
Methaqualone is a sedative-hypnotic medication that was widely prescribed during the mid-20th century. It was marketed under various brand names, including
Methaqualone
System for naming organic chemical compounds
Carboxylic acid derivatives Acid anhydride Esters Acyl halides Amides Imides Amidines −COOCO− −COO− −COX −CONH2 −CONC< −CNHNH2 acyloxy- R-oxycarbonyl- halocarbonyl-
IUPAC nomenclature of organic chemistry
IUPAC_nomenclature_of_organic_chemistry
Chemical group (–CH2–CH3)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Ethyl_group
Organic compound with the structure >C(O–)2
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Acetal
Antiseptic solution
derivatives Ethacridine lactate 9-Aminoacridine Euflavine Biguanides and amidines Dibrompropamidine Chlorhexidine# Propamidine Hexamidine Polihexanide Phenol
Povidone-iodine
Chemical compound
organic compound with the formula C6H5C(NH)NH2. It is the simplest aryl amidine. The compound is a white solid that is slightly soluble in water. It is
Benzamidine
Organic compound containing an –NO2 group
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Nitro_compound
Chemical group (>S(=O)2)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Sulfonyl_group
Chemical group (–C(=O)C6H5
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Benzoyl_group
Heterocyclic aromatic organic compound
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Pyridine
Naturally occurring sedative and hallucinogen
Nielsen B, et al. (2016). Synthesis and Pharmacological Evaluation of Amidine Containing GABAA Receptor Agonists (PDF). EFMC International Symposium
Muscimol
Chemical compound
have been explored. The structure of bottromycin contains a macrocyclic amidine as well as a thiazole ring. The absolute stereochemistry at several chiral
Bottromycin
Type of organosulfur compound
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Sulfinylamine
Chemical group (–C4H9) derived from butane
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Butyl_group
Polyatomic ion (NO3, charge –1) found in explosives and fertilisers
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Nitrate
Chemical compound
nitriles to triazines, and the addition of amines to nitriles to form amidines. PubChem. "Yttrium trifluoromethanesulfonate". pubchem.ncbi.nlm.nih.gov
Yttrium_triflate
Chemical reaction
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Hydrodealkylation
Chemical group (R–O)
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Alkoxy_group
Chemical compound
homolytic bond dissociation energies of the hydrogen-nitrogen bonds in amidines, carboxamides, and thiocarboxamides". Journal of the American Chemical
Benzamide
Organic compound or functional group containing a C=N bond
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Imine
Organic compound with a –C≡N functional group
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Nitrile
Chemical group made of an –S(=O)2 group bound to a halogen
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Sulfonyl_halide
Chemical compound
derivatives Ethacridine lactate 9-Aminoacridine Euflavine Biguanides and amidines Dibrompropamidine Chlorhexidine# Propamidine Hexamidine Polihexanide Phenol
Potassium_permanganate
Chemical compound
Guillaume (2012). "Controlled ROP of β-butyrolactone simply mediated by amidine, guanidine, and phophazene organocatalysts". Macromol. Rapid Commun. 33
Β-Butyrolactone
Chemical reaction which transfers an alkyl group between molecules
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Transalkylation
Functional group
Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite Nitro
Thiosulfinate
AMIDINE
AMIDINE
AMIDINE
AMIDINE
Girl/Female
Welsh
Legendary daughter of GanKy.
Girl/Female
Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Sanskrit, Sindhi
Offering
Boy/Male
Hindu, Indian
Charming; Delightful
Boy/Male
Tamil
Pleasing
Girl/Female
Arabic, Muslim
Graceful; Elegant
Surname or Lastname
English
English : variant of Appling.
Girl/Female
British, English
From Wales
Boy/Male
Arabic
Desire; Object
Girl/Female
Arabic, Muslim, Sindhi
The Daughter of Al-haytam Muhammad Bin Al-haysam was so Named
Boy/Male
Hindu
Lord Shiva
AMIDINE
AMIDINE
AMIDINE
AMIDINE
AMIDINE