ROCK-IN-32

    WARNING: This product is for research use only, not for human or veterinary use.

Hodoodo CAT#: H562877

CAS#: 1013117-40-2

Description: ROCK-IN-32 is a potent Rho--​kinase (ROCK) inhibitor.


Chemical Structure

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ROCK-IN-32
CAS# 1013117-40-2

Theoretical Analysis

Hodoodo Cat#: H562877
Name: ROCK-IN-32
CAS#: 1013117-40-2
Chemical Formula: C20H17Cl2N3O2
Exact Mass: 401.07
Molecular Weight: 402.270
Elemental Analysis: C, 59.72; H, 4.26; Cl, 17.62; N, 10.45; O, 7.95

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @hodoodo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: ROCK-IN-32; ROCK IN 32; ROCKIN32; ROCK-inhibitor-32; ROCK inhibitor 32;

IUPAC/Chemical Name: trans--​4-​(4-​Chlorophenyl)​pyrrolidine-​3-​carboxylic acid N-​(7-​chloro-​1-​oxo-​1,​2-​dihydroisoquinolin-​6-​yl)​amide

InChi Key: XBFAFSAUQFDEOK-CVEARBPZSA-N

InChi Code: InChI=1S/C20H17Cl2N3O2/c21-13-3-1-11(2-4-13)15-9-23-10-16(15)20(27)25-18-7-12-5-6-24-19(26)14(12)8-17(18)22/h1-8,15-16,23H,9-10H2,(H,24,26)(H,25,27)/t15-,16+/m1/s1

SMILES Code: ClC1=CC=C([C@H]2CNC[C@@H]2C(NC3=CC4=C(C(NC=C4)=O)C=C3Cl)=O)C=C1

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 402.27 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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20: Grisk O, Koenen A, Meissner T, Donner A, Braun D, Steinbach A, Glöckl G, Zimmermann U, Evert K, Evert M, Katsari E, Löhn M, Plettenburg O, Rettig R. Rho kinase inhibition mitigates sunitinib-induced rise in arterial pressure and renal vascular resistance but not increased renal sodium reabsorption. J Hypertens. 2014 Nov;32(11):2199-210; discussion 2110. doi: 10.1097/HJH.0000000000000326. PubMed PMID: 25275248.