Transferase
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Transferases are a collection of a large and diverse group of enzymes that specifically catalyze the transfer of one or more functional groups from one molecule (the donor) to another (the acceptor). A few transferases involved in this category include farnesyltransferase (FTase), diacylglycerol acyltransferase (DGAT) and catechol-O-methyltransferase (COMT). Ftase catalyzes the transfer of a farnesyl moiety to the cysteine terminal residue (the sulfhydryl cysteine of the CAAS motif)) of substrate proteins. DGAT catalyzes the final step of the triacylglycerol (TG) biosynthetic pathway, where diacylglycerol is esterified to produce TG. COMT catalyzes the methylation of catechol substrates utilizing S-adenosyl-L-methionine (SAM) as a methyl donor and generating O-methylated catechol and S-adenosyl-L-homocysteine.
Products Related to Transferase(21)
- GC10330LonafarnibCAS: 193275-84-2Purity: >98.50%
A farnesyltransferase inhibitor with antitumor activity
- GC10905Amodiaquine dihydrochloride dihydrateCAS: 6398-98-7Purity: >99.50%
El dihidrocloruro de amodiaquina dihidrato (Dihidrocloruro de amodiaquina dihidrato), una clase de 4-aminoquinolina de agente antipalÚdico, es un inhibidor potente y activo por vÍa oral de la histamina N-metiltransferasa.
- GC12912BCATc Inhibitor 2CAS: 406191-34-2Purity: >99.00%
BCATc Inhibitor 2 es un inhibidor selectivo de la aminotransferasa de cadena ramificada (BCAT) para la investigaciÓn de enfermedades neurodegenerativas.
- GC14308FK866 (APO866)CAS: 658084-64-1Purity: >99.50%
FK866 (APO866) es un inhibidor de la nicotinamida fosforibosiltransferasa (NMPRTase).
- GC15274PF-04620110CAS: 1109276-89-2Purity: >98.00%
PF-04620110 es un inhibidor oralmente activo y selectivo de diacilglicerol aciltransferasa-1 (DGAT1) (IC 50 = 19nM)
- GC15442Tipifarnib (Zarnestra)CAS: 192185-72-1Purity: >98.50%
A farnesyltransferase inhibitor with antitumor activity
- GC16310FTI 277 HClCAS: 180977-34-8Purity: >99.00%
FTI 277 HCl es un inhibdor potente y selectivo de la farnesiltranferasa (FTasa) con un valor de IC 50 de 0.5nM,que muestra una selectividad qproximadamente 100 veces mayor que la geranylgreaniltransferasa I (GGTase I).
- GC16738Tunicamycin MixtureCAS: 11089-65-9Purity: >95.00%
Tunicamycin Mixture es una mezcla de antibióticos nucleósidos homólogos que inhibe la N-glycosylación y bloquea la fosfotransferasa de GlcNAc (GPT).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC10106 | OR-486 | 7659-29-2 | >98% | |
OR-486 (OR-486) es un potente inhibidor de la catecol-O-metiltransferasa, con una IC50 de 12 nM. | ||||
| GC10265 | Manumycin A | 52665-74-4 | >98.00% | |
La manumicina A es un antibiÓtico. | ||||
| GC10330 | Lonafarnib | 193275-84-2 | >98.50% | |
A farnesyltransferase inhibitor with antitumor activity | ||||
| GC10905 | Amodiaquine dihydrochloride dihydrate | 6398-98-7 | >99.50% | |
El dihidrocloruro de amodiaquina dihidrato (Dihidrocloruro de amodiaquina dihidrato), una clase de 4-aminoquinolina de agente antipalÚdico, es un inhibidor potente y activo por vÍa oral de la histamina N-metiltransferasa. | ||||
| GC11524 | Cystamine dihydrochloride | 56-17-7 | >98% | |
transglutaminase inhibitor | ||||
| GC11884 | GPP 78 hydrochloride | - | >98% | |
NAMPT inhibitor | ||||
| GC12449 | SKF 91488 dihydrochloride | 68941-21-9 | >98% | |
histamine N-methyltransferase inhibitor | ||||
| GC12912 | BCATc Inhibitor 2 | 406191-34-2 | >99.00% | |
BCATc Inhibitor 2 es un inhibidor selectivo de la aminotransferasa de cadena ramificada (BCAT) para la investigaciÓn de enfermedades neurodegenerativas. | ||||
| GC12981 | OU749 | 519170-13-9 | >98% | |
γ-Glutamyl transferase (GGT) inhibitor | ||||
| GC14308 | FK866 (APO866) | 658084-64-1 | >99.50% | |
FK866 (APO866) es un inhibidor de la nicotinamida fosforibosiltransferasa (NMPRTase). | ||||
| GC15274 | PF-04620110 | 1109276-89-2 | >98.00% | |
PF-04620110 es un inhibidor oralmente activo y selectivo de diacilglicerol aciltransferasa-1 (DGAT1) (IC 50 = 19nM) | ||||
| GC15442 | Tipifarnib (Zarnestra) | 192185-72-1 | >98.50% | |
A farnesyltransferase inhibitor with antitumor activity | ||||
| GC15614 | A922500 | 959122-11-3 | >98.50% | |
A922500 es un inhibidor potente, selectivo y biodisponible por vía oral de diacilglicerol aciltransferasa 1 (DGAT-1) con valores de IC 50 de 9 y 22nM contra DGAT-1 humano y ratón, respectivamente | ||||
| GC16129 | LY 78335 | 39959-66-5 | >95.00% | |
phenylethanolamine-N-methyltransferase (PNMT) inhibitor | ||||
| GC16310 | FTI 277 HCl | 180977-34-8 | >99.00% | |
FTI 277 HCl es un inhibdor potente y selectivo de la farnesiltranferasa (FTasa) con un valor de IC 50 de 0.5nM,que muestra una selectividad qproximadamente 100 veces mayor que la geranylgreaniltransferasa I (GGTase I). | ||||
| GC16612 | GGsTop | 926281-37-0 | >95.00% | |
GGsTop es un inhibidor irreversible de la γ-glutamyl transpeptidasa (GGT) (K i = 170μM) | ||||
| GC16738 | Tunicamycin Mixture | 11089-65-9 | >95.00% | |
Tunicamycin Mixture es una mezcla de antibióticos nucleósidos homólogos que inhibe la N-glycosylación y bloquea la fosfotransferasa de GlcNAc (GPT). | ||||
| GC17046 | Tris DBA | 51364-51-3 | >98% | |
N-myristoyltransferase-1 (NMT-1) inhibitor | ||||
| GC17780 | FTase Inhibitor II | 156707-43-6 | >98.50% | |
Ftase inhibitor | ||||
| GC17921 | Tolcapone | 134308-13-7 | >98% | |
A reversible COMT inhibitor | ||||
| GC10170 | LB42708 | 226929-39-1 | >98% | |
LB42708 es un inhibidor de la farnesiltransferasa potente, selectivo y activo por vÍa oral. | ||||
