Product Information

Enocitabine is an organic molecule.

CAS No.	55726-47-1
Product Name	Enocitabine

Heavy Atom Count	40	Rotatable Bond Count	23
Atom Stereo Count	4	Bond Stereo Count	0
HBA	8	HBD	4
TPSA	133.910 Å²	Charge	0
Exact Mass	565.40909	Complexity	863.72
pKa	7.130	XLogP	5.615

Studies related to this compound and its mechanism of action

Idarubicin plus behenoyl cytarabine and 6-thioguanine compares favorably with idarubicin plus cytarabine-based regimen for children with previously untreated acute myeloid leukemia: 10-year retrospective, multicenter study in Korea.

Journal of Korean medical science • Vol. 25, Issue 1 • 2010

PMID: 20052341 PMC: PMC2800026 DOI: 10.3346/jkms.2010.25.1.9

The clinical outcome of FLAG chemotherapy without idarubicin in patients with relapsed or refractory acute myeloid leukemia.

Journal of Korean medical science • Vol. 24, Issue 3 • 2009

PMID: 19543516 PMC: PMC2698199 DOI: 10.3346/jkms.2009.24.3.498

Gemtuzumab ozogamicin in combination with attenuated doses of standard induction chemotherapy can successfully induce complete remission without increasing toxicity in patients with acute myeloid leukemia aged 55 or older.

European journal of haematology • Vol. 79, Issue 5 • 2007

PMID: 17916082 DOI: 10.1111/j.1600-0609.2007.00946.x

[Adams-Stokes attack due to complete atrioventricular block in a patient with acute promyelocytic leukemia during remission induction therapy using all-trans retinoic acid].

[Rinsho ketsueki] The Japanese journal of clinical hematology • Vol. 46, Issue 3 • 2005

PMID: 16447716

Enocitabine

In Stock•Starting at $277 for 25 mg•Purity ≥ 98%

CAS No.	55726-47-1
MDL No.	N/A
MF	C₃₁H₅₅N₃O₆
MW	565.80
InChI Key	SAMRUMKYXPVKPA-VFKOLLTISA-N

CUSTOM SYNTHESIS PRECLINICAL SUPPORT

Pricing & Availability

Pack Size	Purity	Price	Availability	Action
25 mg	98%	$277	In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

Enocitabine is an organic molecule.

CAS No.	55726-47-1
Product Name	Enocitabine

Heavy Atom Count	40	Rotatable Bond Count	23
Atom Stereo Count	4	Bond Stereo Count	0
HBA	8	HBD	4
TPSA	133.910 Å²	Charge	0
Exact Mass	565.40909	Complexity	863.72
pKa	7.130	XLogP	5.615

Enocitabine

Pricing & Availability

Product Information

Properties

Enocitabine

Pricing & Availability

Product Information

Properties

Documentation

Enocitabine

Pricing & Availability

Product Information

Properties

Related Articles

Idarubicin plus behenoyl cytarabine and 6-thioguanine compares favorably with idarubicin plus cytarabine-based regimen for children with previously untreated acute myeloid leukemia: 10-year retrospective, multicenter study in Korea.

The clinical outcome of FLAG chemotherapy without idarubicin in patients with relapsed or refractory acute myeloid leukemia.

Gemtuzumab ozogamicin in combination with attenuated doses of standard induction chemotherapy can successfully induce complete remission without increasing toxicity in patients with acute myeloid leukemia aged 55 or older.

[Adams-Stokes attack due to complete atrioventricular block in a patient with acute promyelocytic leukemia during remission induction therapy using all-trans retinoic acid].

Similar Products

N4-Acetylcytidine

Enocitabine

Pricing & Availability

Product Information

Properties

Related Articles

Idarubicin plus behenoyl cytarabine and 6-thioguanine compares favorably with idarubicin plus cytarabine-based regimen for children with previously untreated acute myeloid leukemia: 10-year retrospective, multicenter study in Korea.

The clinical outcome of FLAG chemotherapy without idarubicin in patients with relapsed or refractory acute myeloid leukemia.

Gemtuzumab ozogamicin in combination with attenuated doses of standard induction chemotherapy can successfully induce complete remission without increasing toxicity in patients with acute myeloid leukemia aged 55 or older.

[Adams-Stokes attack due to complete atrioventricular block in a patient with acute promyelocytic leukemia during remission induction therapy using all-trans retinoic acid].

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N4-Acetylcytidine

Documentation