Endocrinology/Hormones
Endocrinology/hormone inhibitors are compounds that block the action of hormones or interfere with hormone signaling pathways. These inhibitors are essential for studying the regulation of endocrine systems and for developing treatments for hormone-related diseases, such as diabetes, thyroid disorders, and hormone-dependent cancers. By modulating hormone activity, these inhibitors can help elucidate the complex interactions within the endocrine system. At CymitQuimica, we offer a wide range of high-quality endocrinology/hormone inhibitors to support your research in endocrinology, pharmacology, and medical sciences.
Subcategories of "Endocrinology/Hormones"
- Androgen Receptor(229 products)
- Annexin A(16 products)
- Aromatase(23 products)
- Estrogen/progestogen Receptor(66 products)
- GPR(1 products)
- Glucocorticoid Receptor(165 products)
- LHRH(2 products)
- Opioid Receptor(327 products)
- Prostaglandin Receptor(122 products)
- RAAS(89 products)
- Reductase(51 products)
- Somatostatin(57 products)
- Thyroid hormone receptor(THR)(33 products)
- Vasopressin Receptor(48 products)
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Found 3420 products of "Endocrinology/Hormones"
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σ1 Receptor/μ Opioid receptor modulator 1
CAS:σ 1 Receptor/ μ Opioid receiver modulator 1 (Compound 44) is an effective σ 1 receptor antagonist (Ki=1.86 nM) and μ Opioid receptor agonists (Ki=2.1 nM).Formula:C24H31FN2O2Color and Shape:SolidMolecular weight:398.51Bopindolol
CAS:Bopindolol: oral β1/β2-ARs antagonist and partial agonist; prodrug of pindolol for hypertension research.Formula:C23H28N2O3Color and Shape:SolidMolecular weight:380.48THPN
CAS:THPN is a Nur77 agonist. It also induces autophagy in melanoma cell lines.Formula:C15H22O4Color and Shape:SolidMolecular weight:266.33Rentiapril
CAS:Rentiapril is an orally active inhibitor of angiotensin converting enzyme (ACE), with antihypertensive activity.Formula:C13H15NO4S2Purity:98%Color and Shape:SolidMolecular weight:313.39ERRα antagonist-1
CAS:ERRα antagonist-1 (ERR+/- antagonist-1) is a high-affinity, selective antagonist of the estrogen-related receptor α (ERRα).Formula:C21H19N3S2Purity:99.66%Color and Shape:SolidMolecular weight:377.53TUG-424
CAS:TUG-424 boosts insulin secretion, is a selective FFAR1 agonist with an EC50 of 32 nM.Formula:C18H16O2Purity:98.94%Color and Shape:SolidMolecular weight:264.32Ref: TM-T17177
1mg77.00€1mL*10mM (DMSO)140.00€5mg150.00€10mg210.00€25mg350.00€50mg522.00€100mg747.00€500mg1,513.00€ALR1/2-IN-1
CAS:ALR1/2-IN-1 (Compound 6e) is an aldehyde reductase (ALR1) (IC50: 3.26 μM) and aldose reductase (ALR2) (IC50: 3.06 μM) inhibitor with anticancer effects.Formula:C18H18N4O5S2Color and Shape:SolidMolecular weight:434.49ES 6864
CAS:ES 6864 is an orally active inhibitor of renin.Formula:C42H58N6O7SColor and Shape:SolidMolecular weight:791.01WAY-267464
CAS:WAY-267464, Non-peptide oxytocin receptor agonist and V1A antagonist, impairs social cognition, used for psychiatric disorders.Formula:C32H35N7O4Purity:99.87%Color and Shape:SolidMolecular weight:581.66TIPP
CAS:TIPP is an agent of delta opioid antagonist.Formula:C37H38N4O6Purity:98%Color and Shape:SolidMolecular weight:634.72Milfasartan
CAS:Milfasartan: Potent AT1 antagonist, oral, effectively reduces blood pressure in hypertensive rats.Formula:C30H30N6O3SColor and Shape:SolidMolecular weight:554.66AS-1669058 oxalate
CAS:AS-1669058 is a G-protein-coupled receptor 119 (GPR119) agonist for the treatment of type 2 diabetes mellitus.Formula:C20H17BrF2N4O5Color and Shape:SolidMolecular weight:511.27SC 46944
CAS:SC 46944 is a highly potent human renin inhibitor.Formula:C34H55N3O7Color and Shape:SolidMolecular weight:617.82Honokiol DCA
CAS:Honokiol DCA inhibits DRP1, enhances respiration via mitochondrial repair, and is active against Vemurafenib-resistant melanoma.Formula:C22H18Cl4O4Color and Shape:SolidMolecular weight:488.19Fidarestat
CAS:Fidarestat (SNK 860),Aldose reductase inhibitor (IC50=26 nM). Targets AKR1B10 (33 μM) and V301L AKR1B10 (1.8 μM). Potential diabetes treatment.Formula:C12H10FN3O4Purity:98%Color and Shape:SolidMolecular weight:279.22Alrestatin Sodium
CAS:Alrestatin is a specific inhibitor of the aldose reductase enzyme.Formula:C14H9NNaO4Purity:98%Color and Shape:SolidMolecular weight:278.219μ opioid receptor agonist 2
CAS:μ opioid receptor agonist 2 （Compound H-3）is a MOR receptor agonist. μ opioid receptor agonist 2 can be used for the research of pain and pain related diseases.Formula:C25H34N4OColor and Shape:SolidMolecular weight:406.56LG-121071
CAS:LG-121071: oral SARM, high-affinity AR full agonist, Ki=17 nM.Formula:C15H15F3N2OPurity:98%Color and Shape:SolidMolecular weight:296.29ATC0065
CAS:ATC0065 is a melanin-concentrating hormone receptor 1 antagonist with oral activity.Formula:C25H29BrF3N5OColor and Shape:SolidMolecular weight:552.43AS1907417
CAS:AS1907417 is a GPR119 agonist.Formula:C19H27N3O4SColor and Shape:SolidMolecular weight:393.5ALR2-IN-3
ALR2-IN-2 inhibits ALR2 strongly (IC50: 22 nM) and ALR1 less (IC50: 116 nM), used in diabetes complication studies.Formula:C17H12N2O3S2Color and Shape:SolidMolecular weight:356.42EMD 66684
CAS:angiotensin AT1 receptor antagonistFormula:C28H31ClN8O2Purity:98%Color and Shape:SolidMolecular weight:547.06TCS 3035
CAS:GPR35 agonist 4 (compound 10), pEC50 5.86, potent in human/rat but inactive with R3.36 mutation.Formula:C12H9NO5SColor and Shape:SolidMolecular weight:279.27Liothyronine HCl
CAS:Liothyronine is a T3 thyroid hormone normally synthesized and secreted by the thyroid gland in much smaller quantities than thyroxine.Formula:C15H13ClI3NO4Purity:98%Color and Shape:SolidMolecular weight:687.43Androgen receptor antagonist 4
CAS:Compound AT2 is an AR inhibitor with anticancer effects, blocking DHT action and AR nuclear translocation (IC50=0.15μM).Formula:C22H18ClNColor and Shape:SolidMolecular weight:331.84RU 752
CAS:RU 752 is an antagonist of mineralocorticoid receptor that inhibits aldosterone synthesis.Formula:C22H30O4Purity:98%Color and Shape:SolidMolecular weight:358.47TFM-4AS-1
CAS:androgen receptor modulatorFormula:C27H33F3N2O2Purity:98%Color and Shape:SolidMolecular weight:474.56FFA1 agonist-1
CAS:FFA1 agonist-1 (Compound 17a) is an orally active fatty acid receptor (FFA1) agonist (EC50: 0.75 μM).Formula:C27H36ClNO3Color and Shape:SolidMolecular weight:458.04ML138
CAS:ML138 is a probe for MLPCN, an agonist of the κ opioid receptor.Formula:C19H14Cl2N4OSColor and Shape:SolidMolecular weight:417.31Estrogen receptor antagonist 2
CAS:ER antagonist 2 selectively suppresses ERα, a key breast cancer driver, with research potential in the disease.Formula:C26H31F4N5Color and Shape:SolidMolecular weight:489.55Xelaglifam
CAS:Xelaglifam is a potent agonist of G protein-coupled receptor 40 (GPR40) and exhibits hypoglycemic effects.Formula:C30H28FNO5Color and Shape:SolidMolecular weight:501.55Estrogen receptor antagonist 1
CAS:"Potent estrogen receptor blocker with promise for breast cancer treatment per WO2021249533A1."Formula:C28H33F4N5Color and Shape:SolidMolecular weight:515.59GSK1104252A
CAS:GSK1104252A is a potent and selective agonist of GPR119.Formula:C22H27FN4O5SPurity:98%Color and Shape:SolidMolecular weight:478.54Gumelutamide
CAS:Gumelutamide, a tetrahydropyridopyrimidine compound, functions as both an antiandrogen and an antineoplastic agent by acting as an androgen antagonist.Formula:C22H21ClN6OColor and Shape:SolidMolecular weight:420.89Aldose reductase-IN-5
CAS:Aldose reductase-IN-5 inhibits ALR2, boosts inhibitory response and antioxidants, slowing diabetes complications.Formula:C18H15NO5Color and Shape:SolidMolecular weight:325.32ALR2-IN-2
ALR2-IN-2 inhibits ALR2 (27 nM IC50) & ALR1 (228 nM IC50), used in diabetes complication research.Formula:C17H11FN2O2S2Color and Shape:SolidMolecular weight:358.41AT1R antagonist 1
CAS:AT1R Antagonist 1 (compound 10) serves as a potent, selective ligand for AT1R with considerable affinity, demonstrated by a K i value of 8.5 nM [1].Formula:C28H32F3N5O4S2Color and Shape:SolidMolecular weight:623.71Glucocorticoid receptor-IN-2
CAS:Glucocorticoid receptor-IN-2 selectively targets GR with anti-inflammatory effects (IC50: 0.171 nM) and activates MMTV (EC50: 0.94 nM).Formula:C25H20F4N6O2Color and Shape:SolidMolecular weight:512.46Levormeloxifene
CAS:Levormeloxifene is a selective modulator of the estrogen receptor. It inhibits the production of vaginal tropoelastin and transforming growth factor-beta 1.Formula:C30H35NO3Purity:98%Color and Shape:SolidMolecular weight:457.6Nitromifene
CAS:Nitromifene is the estrogen receptor antagonist.Formula:C27H28N2O4Purity:98%Color and Shape:SolidMolecular weight:444.52DK3
CAS:DK3 is a potent and selective agonist of estrogen-related receptor alpha (ERRα). ERRα is a potential drug target for cancer and metabolic diseases [1].Formula:C16H14N2O2Color and Shape:SolidMolecular weight:266.29SB-568849
CAS:SB-568849 is a melanin-concentrating hormone receptor 1 antagonist (pKi: 7.7).Formula:C28H31F3N2O3Purity:98%Color and Shape:SolidMolecular weight:500.55FSHR agonist 1
CAS:FSHR agonist 1: high-affinity, allosteric FSHR activator, pEC50 of 7.72, interacts with TMD.Formula:C26H33N3O3SColor and Shape:SolidMolecular weight:467.62SB 706375
CAS:urotensin-II (UT) receptor antagonistFormula:C20H22BrF3N2O5SPurity:98%Color and Shape:SolidMolecular weight:539.36ATC0065 HCl
CAS:ATC0065 dihydrochloride is a novel nonpeptidic and potent melanin-concentrating hormone receptor 1 (MCHR1) selective antagonist.Formula:C25H31BrCl2F3N5OColor and Shape:SolidMolecular weight:625.35(R,R)-THC
CAS:agonist at ERα receptor and antagonist at ERβ receptorFormula:C22H24O2Purity:98%Color and Shape:SolidMolecular weight:320.42LY285434
CAS:LY285434 is a suitable angiotensin II receptor antagonist.Formula:C23H25N5O2Purity:98%Color and Shape:SolidMolecular weight:403.48Chlorothalonil
CAS:Chlorothalonil (DAC 2787): Broad-spectrum, efficient, low-toxicity fungicide for fruits, vegetables, rice, wheat, cotton.Formula:C8Cl4N2Purity:98.01% - 98.71%Color and Shape:Colorless Crystals SolidMolecular weight:265.91FERb 033
CAS:ERβ receptor agonistFormula:C13H9ClFNO3Purity:98%Color and Shape:SolidMolecular weight:281.67Dehydro Olmesartan
CAS:Dehydro Olmesartan, from Olmesartan, is an AT1R blocker for researching hypertension.Formula:C24H24N6O2Color and Shape:SolidMolecular weight:428.49LY 281217
CAS:LY 281217, an organic opioid agonist, can produce analgesic effects in mice.Formula:C32H42N4O6Purity:98%Color and Shape:SolidMolecular weight:578.7Idoxifene
CAS:Idoxifene is a tissue-specific selective estrogen receptor modulator.Formula:C28H30INOPurity:100%Color and Shape:SolidMolecular weight:523.45Ref: TM-T14883
5mgTo inquire10mgTo inquire1mL*10mM (DMSO)To inquire1mg71.00€25mg557.00€50mg964.00€100mg1,639.00€Cyprodinil
CAS:Cyprodinil is a fungicide blocking methionine synthesis in fungi and hinders B. cinerea, P. herpotrichoides, H. oryzae growth; it's also an AR agonist.Formula:C14H15N3Color and Shape:SolidMolecular weight:225.29Pipendoxifene hydrochloride
CAS:Pipendoxifene hydrochloride is a selective modulator of estrogen receptor.Formula:C29H33ClN2O3Purity:99.56%Color and Shape:SolidMolecular weight:493.04Ref: TM-T12482
1mg50.00€5mg105.00€1mL*10mM (DMSO)117.00€10mg170.00€25mg356.00€50mg595.00€100mg982.00€Aldose reductase-IN-4
CAS:Aldose reductase-IN-4 (compund IIc) is an inhibitor of aldose reductase with IC50s of 11.70 μM and 0.98 μM for ALR1 and ALR2, respectively [1].Formula:C14H10FNO3SColor and Shape:SolidMolecular weight:291.3Aldose reductase-IN-6
CAS:AR inhibitor Aldose reductase-IN-6: IC50 3.164 μM, Ki 0.018 μM, non-toxic to normal cells.Formula:C20H16N4O2SColor and Shape:SolidMolecular weight:376.43Olmesartan methyl ester
CAS:Olmesartan methyl ester: an intermediate for synthesizing Olmesartan medoxomil, a strong AT1 receptor blocker.Formula:C25H28N6O3Color and Shape:SolidMolecular weight:460.53SIM-688
CAS:SIM-688 is a selective and orally active estrogen receptor inhibitor of NF-κB transcriptional activity (IC50 = 122 nM in HAECT-1 cells).Formula:C34H31F3N2O2Purity:99.56%Color and Shape:SolidMolecular weight:556.62Zuclomiphene citrate
CAS:Zuclomiphene citrate, a cis isomer of Clomiphene, has stronger antiestrogenic effects and better inhibits LH secretion.Formula:C32H36ClNO8Purity:98%Color and Shape:SolidMolecular weight:598.08Estrogen receptor β antagonist 2
CAS:Estrogen receptor β antagonist 2 is a selective, potent estrogen receptor β (ERβ) antagonist that acts on Erα (IC50: 109.10 μM) and Erβ (IC50: 0.63 μM).Formula:C23H26N2O6Color and Shape:SolidMolecular weight:426.46(R)-DPN
CAS:estrogen receptor (ER) β agonistFormula:C15H13NO2Purity:98%Color and Shape:SolidMolecular weight:239.27JTC-801 free base
CAS:JTC-801 is a selective antagonist of the opioid receptor-like1 receptor (Ki: 8.2 nM).Formula:C26H25N3O2Purity:98%Color and Shape:SolidMolecular weight:411.5Viminol
CAS:Viminol is an opioid analgesic. Viminol is based on the α-pyrryl-2-aminoethanol structure, unlike any other class of opioids.Formula:C21H31ClN2OPurity:98%Color and Shape:SolidMolecular weight:362.94Lubabegron fumarate
CAS:Lubabegron (LY591281, LY488756 fumarate) is a beta-agonist approved in 2018 to lower ammonia in cattle waste, aiding environment and health.Formula:C29H29N3O3SC4H4O4Color and Shape:SolidMolecular weight:557.66GSK706
CAS:GSK706 is a novel effective agonist of the GPR119.Formula:C23H29N5O4SPurity:98%Color and Shape:SolidMolecular weight:471.57Dimethomorph
CAS:Dimethomorph is a fungicide and sterol biosynthesis inhibitor that inhibits fungal cell wall formation,. inhibits androgen receptor (AR) .Formula:C21H22ClNO4Purity:99.20%Color and Shape:Solid CrystallineMolecular weight:387.86FK-739 free acid
CAS:FK-739, an angiotensin II receptor blocker, inhibits rat aorta binding (IC50=8.6 nM) but not bovine cerebellum.Formula:C24H23N7Purity:98%Color and Shape:SolidMolecular weight:409.49Aldose reductase-IN-2
CAS:Aldose reductase-IN-2 (5f) inhibits AR with antioxidant effects; potential anti-diabetic drug.Formula:C25H28N4O5Color and Shape:SolidMolecular weight:464.51HG122
CAS:HG122 promotes AR degradation via proteasome, inhibiting castration-resistant prostate cancer.Formula:C15H13N5O5Color and Shape:SolidMolecular weight:343.29Desketoraloxifene
CAS:Desketoraloxifene is a selective estrogen receptor modulator, inhibiting mammalian PLD (PLD1 and PLD2).Formula:C27H27NO3SPurity:98%Color and Shape:SolidMolecular weight:445.57Org-34517
CAS:Org-34517, a glucocorticoid receptor (GR) antagonist, is used potentially for the treatment of depression.Formula:C28H30O4Purity:98%Color and Shape:SolidMolecular weight:430.54GW7604
CAS:GW7604 is an antiestrogen and it also is the metabolite of GW5638. GW5638 is an antagonist of high-affinity estrogen receptor (ER).Formula:C25H22O3Purity:98%Color and Shape:SolidMolecular weight:370.44ICI 154,129
CAS:Selective δ opioid antagonistFormula:C34H46N4O6SPurity:98%Color and Shape:SolidMolecular weight:638.82Prednisolone Tebutate
CAS:Prednisolone Tebutate is a synthetic glucocorticoid, and is an antiinflammatory and immunosuppressant.Formula:C27H38O6Purity:98%Color and Shape:SolidMolecular weight:458.59Renin inhibitor-1
CAS:Renin inhibitor-1 (compound 26) is a potent, orally active renin inhibitor capable of acting on rh-renin (IC50: 0.9 nM) and hPRA (IC50: 1.8 nM). renal disease.Formula:C22H30N4O4Color and Shape:SolidMolecular weight:414.5Fispemifene
CAS:Fispemifene (HM-101) is an estrogen receptor modulator (SERM) used to treat genitourinary syndromes and vaginal atrophy.Formula:C26H27ClO3Purity:98.74% - 99.67%Color and Shape:SolidMolecular weight:422.94Bopindolol fumarate
CAS:Bopindolol fumarate: non-selective β1/β2-adrenoceptor blocker, partial agonist, low β3 affinity, treats hypertension.Formula:C27H32N2O7Color and Shape:SolidMolecular weight:496.56(1R,2R)-2-PCCA hydrochloride
CAS:(1R,2R)-2-PCCA HCl: Potent, selective GPR88 agonist, crosses BBB, EC50 1140 nM in mouse striatum. Useful for CNS research.Formula:C30H39Cl2N3OPurity:98.75% - 99.67%Color and Shape:SolidMolecular weight:528.56Ref: TM-T13423
2mg97.00€5mg144.00€1mL*10mM (DMSO)166.00€10mg274.00€25mg567.00€50mg747.00€100mg1,017.00€L 364918
CAS:L 364918 is an oxytocin antagonist.Formula:C40H54N8O6Purity:98%Color and Shape:SolidMolecular weight:742.91(R)-Viloxazine Hydrochloride
CAS:(R)-Viloxazine Hydrochloride, the R-isomer of Viloxazine.Formula:C13H20ClNO3Purity:99.88% - 99.94%Color and Shape:SolidMolecular weight:273.76Ref: TM-T22413
1mg52.00€1mL*10mM (DMSO)101.00€5mg111.00€10mg162.00€25mg235.00€50mg330.00€100mg452.00€200mg607.00€PF-3882845
CAS:PF-3882845, a high affinity MR antagonist (IC50=2.7 nM) for hypertension, also targets progesterone receptor (IC50: 310 nM).Formula:C24H22ClN3O2Purity:99.63%Color and Shape:SolidMolecular weight:419.9PF-4455242 HCl
CAS:PF-4455242 HCl is a selective and orally available κ-opioid receptor antagonist that exhibiting antidepressant effects.Formula:C21H29ClN2O2SPurity:99.59%Color and Shape:SolidMolecular weight:408.99AZD2906
CAS:AZD2906: selective GR agonist with human/rat IC50s - 2.2/0.3 nM (PBMC), 41.6/7.5 nM (blood); induces rat bone marrow micronuclei.Formula:C26H25FN4O3Color and Shape:SolidMolecular weight:460.5NNC45-0781
CAS:NNC45-0781 is a tissue-selective partial-agonist of estrogen.Formula:C27H29NO3Purity:98%Color and Shape:SolidMolecular weight:415.52AT2R antagonist 1
CAS:AT2R antagonist 1: potent, selective ligand, Ki 29 nM, inhibits CYP enzymes, stable in liver microsomes.Formula:C23H30N4O4S2Color and Shape:SolidMolecular weight:490.64Capesaris
CAS:Capesaris (GTX-758) is an oral estrogen receptor α agonist, used in prostate cancer research.Formula:C19H13F2NO3Purity:99.65%Color and Shape:SolidMolecular weight:341.31DK1
CAS:DK1: potent ERRα modulator, lowers blood glucose, promising for diabetes research.Formula:C16H13ClN2O2Color and Shape:SolidMolecular weight:300.74LY191704
CAS:LY 191704 is a 5α-reductase type 1 inhibitor.Formula:C14H16ClNOColor and Shape:SolidMolecular weight:249.74LGD-2226
CAS:LGD-2226: selective oral androgen receptor modulator, EC50: 0.2nM, Ki: 1.5nM. Treats muscle loss, osteoporosis, sexual issues.Formula:C14H9F9N2OPurity:98%Color and Shape:SolidMolecular weight:392.22SC 51316
CAS:SC 51316 is a nonpeptidic angiotensin II (AII) receptor antagonist.Formula:C24H29N7OColor and Shape:SolidMolecular weight:431.53Estrogen receptor-IN-1
CAS:Estrogen receptor-IN-1 (compound 16) is an effective estrogen receptor (ER) inhibitor with IC 50 s of 13, 5μM for ERα and Erβ, respectively [1].Formula:C14H16OSiColor and Shape:SolidMolecular weight:228.36GPR40 agonist 1
CAS:GPR40 agonist 1 is an effective new GPR40 agonist (EC50s: 17 nM and 2 nM for rGPR40 and hGPR40).Formula:C27H30FN3O4Purity:98%Color and Shape:SolidMolecular weight:479.54BMS-819881
CAS:BMS-819881 is a melaninconcentrating hormone receptor 1 (MCHR1) antagonist, which binds rat MCHR1 with a Ki of 7 nM and it also is selective and potent forFormula:C24H21ClN2O4SPurity:98%Color and Shape:SolidMolecular weight:468.95Androgen receptor antagonist 3
CAS:Androgen receptor antagonist 3 (Compound C18) has anticancer activities that is an antagonist of androgen receptor (AR) (IC 50 = 2.4 μM) [1].Formula:C22H18ClNColor and Shape:SolidMolecular weight:331.84L162441
CAS:L162441 is an antagonist of Angiotensin type 1 receptor.Formula:C34H43N5O5SPurity:98%Color and Shape:SolidMolecular weight:633.8L-366509
CAS:L-366,509 is an antagonist of oxytocin.Formula:C25H33NO5SPurity:98%Color and Shape:SolidMolecular weight:459.6RU 43044
CAS:RU 43044 is a selective glucocorticoid receptor antagonist that has exhibited an antidepressant-like effect.Formula:C29H34O2Purity:98%Color and Shape:SolidMolecular weight:414.58KB-130015
CAS:KB-130015, a activator of hERG1 potassium channels, blocks native and recombinant hERG1 channels at high voltages.Formula:C18H14I2O4Purity:98%Color and Shape:SolidMolecular weight:548.11OP-1074
CAS:OP-1074 is a pure antiestrogen and a selective degrader of ER, shows specific antiestrogenic activity for ERα and ERβ.Formula:C29H31NO4Purity:98%Color and Shape:SolidMolecular weight:457.56MK-4541
CAS:MK-4541: oral, selective AR modulator, blocks 5α-reductase, curbs AR+ prostate cancer growth, effective in mouse model.Formula:C22H31F3N2O3Color and Shape:SolidMolecular weight:428.49
