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Results for "

Deacetyl

" in MedChemExpress (MCE) Product Catalog:

33

Inhibitors & Agonists

6

Peptides

17

Natural
Products

2

Isotope-Labeled Compounds

2

Click Chemistry

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-G0018
    Norgestimate metabolite Norelgestromin

    17-Deacetyl norgestimate; 17-Deacylnorgestimate

    		 Drug Metabolite Endocrinology
    Norgestimate metabolite Norelgestromin (17-Deacetyl norgestimate) is a metabolite of Norgestimate (HY-W013172). Norgestimate metabolite Norelgestromin is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Norgestimate metabolite Norelgestromin
  • HY-20584
    10-Deacetyl-7-xylosyl paclitaxel

    10-Deacetyl-7-xylosyltaxol; 10-Deacetylpaclitaxel 7-Xyloside; 10-Deacetyltaxol 7-Xyloside

    		 Microtubule/Tubulin ADC Payload Cancer
    10-Deacetyl-7-xylosyl paclitaxel is a Paclitaxel (a microtubule stabilizing agent; enhances tubulin polymerization) derivative with improved pharmacological features.
    10-Deacetyl-7-xylosyl paclitaxel
  • HY-14959
    Ulipristal

    CDB-3236; Deacetyl CDB-2914

    		 Progesterone Receptor Endocrinology Cancer
    Ulipristal (CDB 3236) is a selective progesterone receptor modulator (SPRM). Ulipristal binds to the progesteron receptor, thereby inhibiting PR-mediated gene expression, and interfering with progesterone activity in the reproductive system .
    Ulipristal
  • HY-P2161B
    TAK-683 acetate
    4 Publications Verification

    		 Kisspeptin Receptor Cancer
    TAK-683 acetate is a potent full KISS1 receptor (KISS1R) agonist (IC50=170 pM) with improved metabolic stability. TAK-683 acetate is a nonapeptide metastin analog, exhibits agonistic activities to KISS1R with EC50 values of 0.96 nM and 1.6 nM for human and rat, respectively . TAK-683 acetate depletes GnRH in the hypothalamus and reduces plasma FSH, LH, and testosterone levels in vivo, it has the potential for the study of hormone-dependent prostate cancer .
    TAK-683 acetate
  • HY-77572
    7-Epi 10-desacetyl paclitaxel

    7-epi-10-Deacetyltaxol; 10-Deacetyl-7-epipaclitaxel

    		 ADC Payload Cancer
    7-Epi 10-desacetyl paclitaxel (7-epi-10-deacetyltaxol), a taxol derivative, exhibits cytotoxicity against HeLa cells with an IC50 of 85 μM .
    7-Epi 10-desacetyl paclitaxel
  • HY-P5544
    M-TriDAP

    N-Acetylmuramyl-L-Ala-γ-D-Glu-meso-diaminopimelic acid

    		 NOD-like Receptor (NLR) Others
    M-TriDAP (N-Acetylmuramyl-L-Ala-γ-D-Glu-meso-diaminopimelic acid) is a NOD1/2 agoist and biological active peptide .
    M-TriDAP
  • HY-N3501
    Deacetyl Ganoderic Acid F

    		Others Metabolic Disease
    Deacetyl Ganoderic Acid F is a 7-anostane triterpenoid from Ganoderma lucidum.
    Deacetyl Ganoderic Acid F
  • HY-P2161
    TAK-683

    		Kisspeptin Receptor Cancer
    TAK-683 is a potent full KISS1 receptor (KISS1R) agonist (IC50=170 pM) with improved metabolic stability. TAK-683 is a nonapeptide metastin analog, exhibits agonistic activities to KISS1R with EC50 values of 0.96 nM and 1.6 nM for human and rat, respectively . TAK-683 depletes GnRH in the hypothalamus and reduces plasma FSH, LH, and testosterone levels in vivo, it has the potential for the study of hormone-dependent prostate cancer .
    TAK-683
  • HY-Z8644
    N-Deacetyl-N-formylcolchicine

    N-Formyl-N-Deacetylcolchicine

    		 Microtubule/Tubulin Apoptosis Cancer
    N-Deacetyl-N-formylcolchicine (N-Formyl-N-deacetylcolchicine, Compound 11) is a selective inhibitor targeting the colchicine-binding site of tubulin. N-Deacetyl-N-formylcolchicine shows antiproliferative activity against various cancer cell lines with IC50 values of 32.61-100.28 nM. N-Deacetyl-N-formylcolchicine inhibits microtubule polymerization to block cell division, induces cancer cell apoptosis and suppresses migration. N-Deacetyl-N-formylcolchicine is promising for research of cancers such as lung cancer and various solid tumors .
    N-Deacetyl-N-formylcolchicine
  • HY-Z8147
    16-O-Deacetyl fusidic acid lactone

    16-Deacetylfusidic acid γ-lactone

    		 Bacterial Infection
    16-O-Deacetyl fusidic acid lactone (16-Deacetylfusidic acid γ-lactone) (FA-9) is a Fusidic acid (HY-B1350) (FA) lactone derivative with antibacterial effects. 16-O-Deacetyl fusidic acid lactone is effective against Gram-positive bacteria, but has no inhibitory effect on Gram-negative bacteria .
    16-O-Deacetyl fusidic acid lactone
  • HY-77572R
    7-Epi 10-desacetyl paclitaxel (Standard)

    7-epi-10-Deacetyltaxol (Standard); 10-Deacetyl-7-epipaclitaxel (Standard)

    		 ADC Payload Reference Standards Cancer
    7-Epi 10-desacetyl paclitaxel (Standard) is the analytical standard of 7-Epi 10-desacetyl paclitaxel. This product is intended for research and analytical applications. 7-Epi 10-desacetyl paclitaxel (7-epi-10-deacetyltaxol), a taxol derivative, exhibits cytotoxicity against HeLa cells with an IC50 of 85 μM .
    7-Epi 10-desacetyl paclitaxel (Standard)
  • HY-G0018S
    Norgestimate metabolite norelgestromin-d6

    17-Deacetyl norgestimate-d6; 17-Deacylnorgestimate-d6

    		 Isotope-Labeled Compounds Drug Metabolite Others
    Norgestimate metabolite norelgestromin-d6 is the deuterium labeled Norgestimate metabolite norelgestromin. Norelgestromin is a metabolite of Norgestimate, which is a progestin or synthetic progestogen. Norgestimate metabolite norelgestromin-d6 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Norgestimate metabolite norelgestromin-d6
  • HY-P2115
    Ramorelix

    		GnRH Receptor Cancer
    Ramorelix is a luteinizing-hormone-releasing hormone (LHRH) antagonist. Ramorelix can inhibit tumor progression in vivo. Ramorelix can be studied in anti-cancer research .
    Ramorelix
  • HY-W778562
    10-Deacetyl-13-oxobaccatin III

    		Others Cancer
    10-Deacetyl-13-oxobaccatin III is an taxane that can be isolated from Taxus sumatrana. 10-Deacetyl-13-oxobaccatin III (30 μg/mL) shows cytotoxicity against A498, NCI-H226, A549, PC-3 cells, with inhibition a rate of 29.7%, 49.2%, 43.9%, 65.3% .
    10-Deacetyl-13-oxobaccatin III
  • HY-W778546
    7-epi-10-Deacetyl baccatin III

    		Others Cancer
    7-epi-10-Deacetyl baccatin III can be isolated from the degradation impurities in Docetaxel (HY-B0011) .
    7-epi-10-Deacetyl baccatin III
  • HY-N9222
    9-Deacetyl-9-benzoyl-10-debenzoyltaxchinin A

    		Others Others
    9-Deacetyl-9-benzoyl-10-debenzoyltaxchinin A is a Diterpenoids product that can be isolated from the stem-barks of Taxus baccata L. cv. stricta. .
    9-Deacetyl-9-benzoyl-10-debenzoyltaxchinin A
  • HY-N1640
    1-O-Deacetyl-2α-hydroxykhayanolide E

    		Others Others
    1-O-Deacetyl-2α-hydroxykhayanolide E is a natural product that can be isolated from Swietenia mahagoni. 1-O-Deacetyl-2α-hydroxykhayanolide E is widely distributed in the leaves and branches of Swietenia mahagoni .
    1-O-Deacetyl-2α-hydroxykhayanolide E
  • HY-W778547
    7-epi-10-Oxo-10-deacetyl baccatin III

    10-Dehydrobaccatin V

    		 Drug Intermediate Cancer
    7-epi-10-Oxo-10-deacetyl baccatin III (10-Dehydrobaccatin V) can be isolated from the degradation impurities in Docetaxel (HY-B0011) .
    7-epi-10-Oxo-10-deacetyl baccatin III
  • HY-N9033
    9-Deacetyl-9-benzoyl-10-debenzoyl-4β,20-epoxytaxchinin A

    		Others Others
    9-Deacetyl-9-benzoyl-10-debenzoyl-4β,20-epoxytaxchinin A is a Diterpenoids product that can be isolated from the stem-barks of Taxus baccata L. cv. stricta. .
    9-Deacetyl-9-benzoyl-10-debenzoyl-4β,20-epoxytaxchinin A
  • HY-125374A
    Larotaxel dihydrate

    XRP9881 dihydrate

    		 Microtubule/Tubulin Cancer
    Larotaxel (dihydrate) (XRP9881 (dihydrate)), a new taxane compound prepared by partial synthesis from 10-deacetyl baccatin III, is active against tumors .
    Larotaxel dihydrate
  • HY-G0018R
    Norgestimate metabolite Norelgestromin (Standard)

    17-Deacetyl norgestimate(Standard); 17-Deacylnorgestimate (Standard)

    		 Reference Standards Drug Metabolite Others
    Norgestimate metabolite Norelgestromin (Standard) is the analytical standard of Norgestimate metabolite Norelgestromin. This product is intended for research and analytical applications.
    Norgestimate metabolite Norelgestromin (Standard)
  • HY-P5544A
    M-TriDAP TFA

    N-Acetylmuramyl-L-Ala-γ-D-Glu-meso-diaminopimelic acid TFA

    		 NOD-like Receptor (NLR) Others
    M-TriDAP (N-Acetylmuramyl-L-Ala-γ-D-Glu-meso-diaminopimelic acid) TFA is a NOD1/2 agoist and biological active peptide .
    M-TriDAP TFA
  • HY-14959S
    Ulipristal-d3

    CDB-3236-d3; Deacetyl CDB-2914-d3

    		 Isotope-Labeled Compounds Progesterone Receptor Endocrinology Cancer
    Ulipristal-d3 (CDB-3236-d3) is deuterium labeled Ulipristal. Ulipristal (CDB 3236) is a selective progesterone receptor modulator (SPRM). Ulipristal binds to the progesteron receptor, thereby inhibiting PR-mediated gene expression, and interfering with progesterone activity in the reproductive system .
    Ulipristal-d3
  • HY-P2161A
    TAK-683 TFA

    		Kisspeptin Receptor Cancer
    TAK-683 TFA is a potent full KISS1 receptor (KISS1R) agonist (IC50=170 pM) with improved metabolic stability. TAK-683 TFA is a nonapeptide metastin analog, exhibits agonistic activities to KISS1R with EC50 values of 0.96 nM and 1.6 nM for human and rat, respectively . TAK-683 TFA depletes GnRH in the hypothalamus and reduces plasma FSH, LH, and testosterone levels in vivo, it has the potential for the study of hormone-dependent prostate cancer .
    TAK-683 TFA
  • HY-N18321
    3-Deacetyl-4-demethylsalannin

    		Drug Derivative Cancer
    3-Deacetyl-4-demethylsalannin, a salannin-type limonoid, is an anticancer agent. 3-Deacetyl-4-demethylsalannin induces cytotoxic activity against leukemia cells and stomach cancer cells, and shows inactivity against lung and breast cancer cells at concentrations up to 100 μM. 3-Deacetyl-4-demethylsalannin can be used for the research of leukemia, stomach cancer .
    3-Deacetyl-4-demethylsalannin
  • HY-N18214
    3-Deacetyl-1,6-diacetylsendanal

    		Drug Derivative Cancer
    3-Deacetyl-1,6-diacetylsendanal is a limonoid compound isolated from the fruits of Melia azedarach. 3-Deacetyl-1,6-diacetylsendanal reduces the viability of leukemia and gastric cancer cells. 3-Deacetyl-1,6-diacetylsendanal can be used in research related to leukemia and gastric cancer .
    3-Deacetyl-1,6-diacetylsendanal
  • HY-W778558
    2-Debenzoyl-2-tigloyl 10-Deacetyl Baccatin III

    		Drug Derivative Others
    2-Debenzoyl-2-tigloyl 10-Deacetyl Baccatin III is a Baccatin III (HY-N6985) derivative lacking a benzoyl residue. 2-Debenzoyl-2-tigloyl 10-Deacetyl Baccatin III can be isolated from the needles of the European yew (T. barcata L.) .
    2-Debenzoyl-2-tigloyl 10-Deacetyl Baccatin III
  • HY-131559
    N-Deacetyl-SI-109-(OEt)2

    		Ligands for Target Protein for PROTAC STAT Cancer
    N-Deacetyl-SI-109-(OEt)2 (Compound 11) is a STAT3 ligand. N-Deacetyl-SI-109-(OEt)2 serves as a Ligand for target protein for the synthesis of STAT3 PROTAC degraders, such as SD-36 (HY-129602). N-Deacetyl-SI-109-(OEt)2 is applicable for cancer research .
    N-Deacetyl-SI-109-(OEt)2
  • HY-182980
    N-(8-Carboxyoctanoyl)-deacetyl BMS-202

    		Target Protein Ligand-Linker Conjugates PD-1/PD-L1 Cancer
    N-(8-Carboxyoctanoyl)-deacetyl BMS-202 is a target protein ligand-linker conjugate. N-(8-Carboxyoctanoyl)-deacetyl BMS-202 contains the target protein PD-1/PD-L1 ligand and a PROTAC linker. N-(8-Carboxyoctanoyl)-deacetyl BMS-202 can be used for the synthesis of PROTAC PD-L1 Degrader-3 (HY-182959) .
    N-(8-Carboxyoctanoyl)-deacetyl BMS-202
  • HY-N18115
    3-O-Deacetyl-3-O-tigloylsalannin

    		Drug Derivative Cancer
    3-O-Deacetyl-3-O-tigloylsalannin is a salannin-type limonoid and cytotoxic agent found in the fruits of Melia azedarach. 3-O-Deacetyl-3-O-tigloylsalannin can be used for the research of leukemia, stomach cancer, breast cancer .
    3-O-Deacetyl-3-O-tigloylsalannin
  • HY-N18291
    12β-1-O-Tigloyl-1-O-deacetyl-nimbolinin B

    		Others Others
    12β-1-O-Tigloyl-1-O-deacetyl-nimbolinin B (Compound 1b) is a nimbolinin-type limonoid found in the fruits of Melia toosendan.12β-1-O-Tigloyl-1-O-deacetyl-nimbolinin B exists as a tautomer of 12α-1-O-tigloyl-1-O-deacetyl-nimbolinin B .
    12β-1-O-Tigloyl-1-O-deacetyl-nimbolinin B
  • HY-N19814
    3'-Deacetylfusicoccin A

    3'-Deacetyl-FC A ; Fusicoccin C

    		 Others Others
    3'-Deacetylfusicoccin A (3'-Deacetyl-FC A; Fusicoccin C) is a fusicoccin that belongs to the 5-8-5 tricyclic diterpenoid glycosides. It can be isolated from the culture filtrate of the Niigata 2-A isolate of Phomopsis amygdali .
    3'-Deacetylfusicoccin A
  • HY-129230
    Triletide

    		Endogenous Metabolite Cardiovascular Disease
    Triletide is a thromboxane A2 antagonist with good oral absorption activity. The biotransformation of Triletide mainly includes the formation of demethyl, deacetyl, demethyl-deacetyl and hydroxy derivatives. The distribution half-life of Triletide is about 1 hour, and the elimination half-life is about 5 hours .
    Triletide

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