GLPBio

Tacalcitol

Catalog No.: GC10890Purity:>98.50%
Tacalcitol is a calcitriol analogue, regulates calcium metabolism by stimulating intestinal calcium absorption and influencing bone turnover.

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


Tacalcitol
Cas No.: 57333-96-7
1mgIn Stock
$69.00
1
5mgIn Stock
$224.00
1
10mgIn Stock
$358.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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الوصف (Description)

Tacalcitol is a calcitriol analogue, regulates calcium metabolism by stimulating intestinal calcium absorption and influencing bone turnover. But tacalcitol has no significant change in bone formation [1]. Tacalcitol can be used in the research of inflammation, breast cancer, and skin diseases, and prevent the osteoporosis that results from the development of cancer or from chemotherapy or hormone therapy [2-3].

In vitro, treatment of normal human keratinoeytes with tacalcitol (0.01-1μM; 48h) increased the numbers of involucrin positive cells and induced cell differentiation [4].

In vivo, tacalcitol (1.0µg/kg; s.c.; thrice weekly) decreased bone column density, transiently decreased the metastatic spread of 4T1 breast carcinoma without influencing primary tumour growth or angiogenesis in old ovariectomized (OVX) mice [2]. While tacalcitol (1.0µg/kg; s.c.; thrice weekly) increased metastatic spread in young mice bearing 4T1 breast cancer [5].

References:
[1] Yamada, S., J-P. Bonjour, and H. Fleisch. "Effect of 1α, 24 (R)-dihydroxyvitamin D3 on calcium metabolism in the rat." European Journal of Endocrinology 111.4 (1986): 572-576.
[2] Anisiewicz, Artur, et al. "Calcitriol analogues decrease lung metastasis but impair bone metabolism in aged ovariectomized mice bearing 4T1 mammary gland tumours." Aging and disease 10.5 (2019): 977.
[3] Matsumoto, Kunio, et al. "Effect of 1, 24R‐dihydroxyvitamin D3 on the growth of human keratinocytes." The Journal of Dermatology 17.2 (1990): 97-103.
[4] Kobayashi, Teruaki, et al. "1α, 24R‐dihydroxyvitamin D3 has an ability comparable to that of 1α,25‐dihydroxyvitamin D3 to induce keratinocyte differentiation." The Journal of Dermatology 17.11 (1990): 707-709.
[5] Anisiewicz, Artur, et al. "Unfavorable effect of calcitriol and its low-calcemic analogs on metastasis of 4T1 mouse mammary gland cancer." International journal of oncology 52.1 (2018): 103-126.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

Human keratinocytes

Preparation Method

Cells were cultured in the presence or absence of tacalcitol (1,24R(OH)2D3); or 1,25(OH)2D3, for 48h. Cells were immunochemically stained using anti-involucrin antibody, and the number of cells expressing involucrin was determined by Flow cytometry using a FACScan.

Reaction Conditions

0.01-1μM; 48h

Applications

The treatment with tacalcitol increased the numbers of involucrin positive cells.

Animal experiment [2]:

Animal models

60 weeks old ovariectomized (OVX) mice bearing 4T1 tumours

Preparation Method

Tacalcitol were administered subcutaneously (s.c.) thrice weekly starting from day 7 after tumor cell inoculation. The single dose of compounds was as follows: calcitriol, 0.5µg/kg; Tacalcitol, 1.0µg/kg; and PRI-2205, 10.0µg/kg. Control mice (both OVX and sham operated) were administered with vehicle (80% PEG) in the same volume and scheme as vitamin D compounds.

Dosage form

1.0µg/kg; s.c.; thrice weekly

Applications

Tacalcitol transiently decreased the metastatic spread of 4T1 breast carcinoma without influencing primary tumour growth or angiogenesis in old OVX mice.

References:
[1] Kobayashi, Teruaki, et al. "1α, 24R‐dihydroxyvitamin D3 has an ability comparable to that of 1α, 25‐dihydroxyvitamin D3 to induce keratinocyte differentiation." The Journal of Dermatology 17.11 (1990): 707-709.
[2] Anisiewicz, Artur, et al. "Calcitriol analogues decrease lung metastasis but impair bone metabolism in aged ovariectomized mice bearing 4T1 mammary gland tumours." Aging and disease 10.5 (2019): 977.

وثائق المنتج (Product Documents)

Purity:>98.50%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
57333-96-7
الاسم الكيميائي
(1R,3S,5Z)-5-[(2E)-2-[(1R,3aS,7aR)-1-[(2R,5R)-5-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexane-1,3-diol
SMILES
CC(C)C(CCC(C)C1CCC2C1(CCCC2=CC=C3CC(CC(C3=C)O)O)C)O
الصيغة الجزيئية
C27H44O3
الوزن الجزيئي
416.65
الذوبانية
20mg/mL in DMSO, 20mg/mL in DMF, 20mg/mL in Ethanol
التخزين
Store at -20°C,unstable in solution, ready to use.
إرشادات عامة
اختر مذيبًا مناسبًا وفقًا لبيانات ذوبانية المنتج. بعد التحضير، قسّم المحلول المخزون إلى أجزاء لتجنب دورات التجميد والذوبان المتكررة.
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
شروط الشحن
تُشحن عينات التقييم مع عبوات تبريد. وتُشحن الأحجام الأخرى المتاحة في درجة حرارة الغرفة، أو مع عبوات تبريد عند الطلب.

الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية

g/mol

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